Results for:
Species: Trichoderma hamatum

(2R,5R)-2-methyl-5-propan-2-ylcyclohexan-1-one

Compound Details

Synonymous names
Tetrahydrocarvone
(R,R)-Tetrahydrocarvone
Carvomenthone, (+-)-
(+)-carvomenthone
(+-)-Carvomenthone
(+-)-Tetrahydrocarvone
N2VIB4RXFK
UNII-N2VIB4RXFK
(+-)-(R,R)-Tetrahydrocarvone
trans-p-Menthan-2-one
p-Menthan-2-one, trans-
D5PYY1B83Q
(1R,4R)-p-Menthan-2-one, (+-)-
p-Menthan-2-one, (1R,4R)-(+-)-
Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (2R,5R)-
5206-83-7
Cyclohexanone, 2-methyl-5-(1-methylethyl)-, (2R-trans)-
p-Menthan-2-one
Cyclohexanone, 2-methyl-5-(1-methylethyl)-, trans-
5-Isopropyl-2-methylcyclohexanone, trans-
5-Isopropyl-2-methyl-cyclohexanone
(2R,5R)-2-methyl-5-propan-2-ylcyclohexan-1-one
trans-5-Isopropyl-2-methylcyclohexanone
(E)-para-menthan-2-one
FEMA No. 3176
trans-5-Isopropyl-2-methylcyclohexan-1-one
trans-Cyclohexanone, 2-methyl-5-(1-methylethyl)-
UNII-D5PYY1B83Q
(+)-TETRAHYDROCARVONE
CARVOMENTHONE, (+)-
SCHEMBL20608621
DTXSID70200035
P-MENTHAN-2-ONE [FHFI]
(+/-)-P-MENTHAN-2-ONE
EINECS 207-887-5
(+)-(R,R)-TETRAHYDROCARVONE
NS00080177
(1R,4R)-P-MENTHAN-2-ONE, (+)-
P-MENTHAN-2-ONE, (1R,4R)-(+)-
(2R,5R)-5-Isopropyl-2-methylcyclohexan-1-one
2-Methyl-5-(1-methylethyl)cyclohexanone, trans-
CYCLOHEXANONE, 2-METHYL-5-(1-METHYLETHYL)-, (2R,5R)-REL-
Microorganism:

Yes

IUPAC name(2R,5R)-2-methyl-5-propan-2-ylcyclohexan-1-one
SMILESCC1CCC(CC1=O)C(C)C
InchiInChI=1S/C10H18O/c1-7(2)9-5-4-8(3)10(11)6-9/h7-9H,4-6H2,1-3H3/t8-,9-/m1/s1
FormulaC10H18O
PubChem ID10997258
Molweight154.25
LogP2.7
Atoms11
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationterpenes ketones

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


1-methyl-4-propan-2-ylcyclohexa-1,4-diene

Mass-Spectra

Compound Details

Synonymous names
GAMMA-TERPINENE
99-85-4
p-Mentha-1,4-diene
Crithmene
Moslene
gamma-Terpinen
1,4-p-Menthadiene
4-Isopropyl-1-methyl-1,4-cyclohexadiene
.gamma.-Terpinen
TERPINENE, ALPHA
.gamma.-Terpinene
1-methyl-4-propan-2-ylcyclohexa-1,4-diene
1,4-Cyclohexadiene, 1-methyl-4-(1-methylethyl)-
1-Isopropyl-4-methyl-1,4-cyclohexadiene
1-Methyl-4-(1-methylethyl)-1,4-cyclohexadiene
FEMA No. 3559
gamma-Terpinene (natural)
1-Methyl-4-isopropylcyclohexadiene-1,4
1-isopropyl-4-methylcyclohexa-1,4-diene
NSC 21448
1-methyl-4-(propan-2-yl)cyclohexa-1,4-diene
UNII-4YGF4PQP49
1,4-Cyclohexadiene, 1-methyl-4-isopropyl-
EINECS 202-794-6
4YGF4PQP49
1-Methyl-4-isopropyl-1,4-cyclohexadiene
DTXSID6041210
CHEBI:10577
AI3-26468
NSC-21448
DTXCID4021210
MFCD00001537
Crithmene; Moslene; NSC 21448; gamma-Terpinene
Gamma-terpinene gamma-terpinene
Alpha terpinene
Gamma terpinene
-terpinene
gamma -Terpinene
Terpinene, .gamma.-
? TERPINENE
?-TERPINENE
gamma-Terpinene, 97%
1-isopropyl-4-methyl-cyclohexa-1,4-diene
|A-TPN
bmse000778
1, 1-methyl-4-isopropyl-
GAMMA-TERPINENE [FCC]
CHEMBL449693
gamma-Terpinene, >=95%, FG
NSC21448
gamma-Terpinene, analytical standard
Tox21_300963
WLN: L6U CUTJ AY1&1 D1
gamma-Terpinene, natural, 95%, FG
P-MENTHA-1,4-DIENE [FHFI]
AKOS015840812
1ST1650
HY-W020183
LMPR0102090027
CAS-99-85-4
NCGC00248232-01
NCGC00254865-01
BS-23574
gamma-Terpinene, purum, >=97.0% (GC)
1-Isopropyl-4-methyl-1,4-cyclohexadiene #
M0318
NS00013198
C09900
E80754
EN300-211578
Q423975
W-100015
Z1255382936
gamma-Terpinene, primary pharmaceutical reference standard
InChI=1/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8H,5-6H2,1-3H
9NI
Microorganism:

Yes

IUPAC name1-methyl-4-propan-2-ylcyclohexa-1,4-diene
SMILESCC1=CCC(=CC1)C(C)C
InchiInChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,7-8H,5-6H2,1-3H3
FormulaC10H16
PubChem ID7461
Molweight136.23
LogP2.8
Atoms10
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10577
Supernatural-IDSN0452646

mVOC Specific Details

MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAHeddergott et al. 2014
EukaryotaPythium OligandrumN/APythium oligandrum GAQ1 strain was isolated from soil from a field where infected ginger was growing in Laiwu district, Jinan City, Shandong Province, China. China General Microbiological Culture Collection Center (CGMCC) deposit number No. 17470.Sheikh et al. 2023
EukaryotaHypoxylon AnthochroumNAMacías-Rubalcava et al. 2018
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAmanita OvoideaFranceBreheret et al. 1997
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
ProkaryotaCollimonas Pratensisnarhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
ProkaryotaCollimonas Pratensisn/aNAGarbeva et al. 2014
EukaryotaTrichoderma Atroviridenawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
EukaryotaTrichoderma AtrovirideNAStoppacher et al. 2010
Kluyveromyces MarxianusJi et al. 2024
Saccharomyces CerevisiaeJi et al. 2024
Enterobacter CloacaeTallon et al. 2023
Klebsiella OxytocaTallon et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBrianSPME/GC-MSno
EukaryotaPythium OligandrumV8 juice agarSPME/GC-MS/MSno
EukaryotaHypoxylon Anthochroumrice medium (RM, 300g of rice and 300ml of water)SPME, GC-MSyes
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
ProkaryotaCollimonas Pratensissand containing artificial root exudatesGC/MSno
ProkaryotaCollimonas PratensisHeadspace trapping/GC-MSno
EukaryotaTrichoderma Atroviridemalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
Kluyveromyces MarxianusSauce Meat during StorageSPME–GC–MSno
Saccharomyces CerevisiaeSauce Meat during StorageSPME–GC–MSno
Enterobacter Cloacaetryptone soya broth (TSB) mediaTenax/GC/MSno
Klebsiella Oxytocatryptone soya broth (TSB) mediaTenax/GC/MSno


(1R,4S,5S)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene

Compound Details

Synonymous names
24048-44-0
(1R,4S,5S)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene
Acoradiene
DTXSID60946894
DVBSKQAFCDJNSL-QLFBSQMISA-N
1,8-Dimethyl-4-(1-methylethenyl)-spiro(4,5)dec-7-ene (1R-(1alpha,4beta,5beta))-
Spiro(4,5)dec-7-ene, 1,8-dimethyl-4-(1-methylethenyl)-, (1R-(1alpha,4beta,5beta))-
1,8-dimethyl-4-(1-methylethenyl)spiro(4.5)dec-7-ene
1,8-DIMETHYL-4-(PROP-1-EN-2-YL)SPIRO[4.5]DEC-7-ENE
Microorganism:

No

IUPAC name(1R,4S,5S)-1,8-dimethyl-4-prop-1-en-2-ylspiro[4.5]dec-8-ene
SMILESCC1CCC(C12CCC(=CC2)C)C(=C)C
InchiInChI=1S/C15H24/c1-11(2)14-6-5-13(4)15(14)9-7-12(3)8-10-15/h7,13-14H,1,5-6,8-10H2,2-4H3/t13-,14+,15-/m1/s1
FormulaC15H24
PubChem ID90351
Molweight204.35
LogP5.1
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID172926
Supernatural-IDSN0076261-04

mVOC Specific Details


Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus TerreusYPDTD/GC-MSno
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno


(1R,4aS,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene

Compound Details

Synonymous names
(-)-gamma-cadinene
GAMMA-CADINENE
1460-97-5
2GHT32E0JU
39029-41-9
(1R,4aS,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
gamma-Cadinene, (-)-
(1R,4aS,8aS)-7-methyl-4-methylidene-1-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
UNII-2GHT32E0JU
g-Cadinene
D-g-Cadinene
(+)-g-Cadinene
Racemic gamma Cadinene
trans- .gamma.-Cadinene
CHEBI:63203
WRHGORWNJGOVQY-RBSFLKMASA-N
DTXSID301017689
.GAMMA.-CADINENE, (-)-
HY-N9432
CADINENE, .GAMMA.-, (-)-
CS-0167725
NS00126425
C19738
1BETA,6ALPHA,7BETAH-CADINA-4,10(15)-DIENE
Q27132466
1.BETA.,6.ALPHA.,7.BETA.H-CADINA-4,10(15)-DIENE
[1R,(-)]-1,2,3,4,4aalpha,5,6,8abeta-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene
1,2,3,4,4a,5,6,8a-Octahydro-7-methyl-4-methylene-1-(1-methylethyl)-(1S,4aR,8aR)-Naphthalene
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4-methylene-1-(1-methylethyl)-, (1alpha,4abeta,8aalpha)-
Microorganism:

No

IUPAC name(1R,4aS,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
SMILESCC1=CC2C(CC1)C(=C)CCC2C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13-15H,4-8H2,1-3H3/t13-,14-,15-/m1/s1
FormulaC15H24
PubChem ID92313
Molweight204.35
LogP4.3
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID63203
Supernatural-IDSN0417892-05

mVOC Specific Details


Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaAntrodia CinnamomeaPDAGC/MSyes
EukaryotaAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


(5R)-2-methyl-5-[(2S)-6-methylhept-5-en-2-yl]cyclohexa-1,3-diene

Compound Details

Synonymous names
Zingiberene
495-60-3
alpha-Zingiberene
.alpha.-Sesquiphellandrene
(5R)-2-methyl-5-[(2S)-6-methylhept-5-en-2-yl]cyclohexa-1,3-diene
8XOC63EI5F
(-)-Zingiberene
a-zingiberene
Zingiberene from ginger
(R)-2-Methyl-5-((S)-6-methylhept-5-en-2-yl)cyclohexa-1,3-diene
[S-(R*,S*)]-5-(1,5-dimethylhexen-4-yl)-2-methyl-1,3-cyclohexa-1,3-diene
UNII-8XOC63EI5F
(S-(R*,S*))-5-(1,5-Dimethylhexen-4-yl)-2-methyl-1,3-cyclohexa-1,3-diene
EINECS 207-804-2
(-)-Zingiberene; l-Zingiberene; -Zingiberene
(-)-alpha-zingiberene
CHEBI:10115
DTXSID00197808
1,3-Cyclohexadiene, 5-[(1S)-1,5-dimethyl-4-hexenyl]-2-methyl-, (5R)-
AKOS028112427
LMPR0103060002
HY-14618
MS-23112
CS-0003477
NS00022237
C09750
G13993
Q4117486
(5r)-2-methyl-5-[(2s)-6-methylhept-5-en-2yl] cyclohexa-1,3-diene
(5R)-5-[(1S)-1,5-dimethyl-4-hexenyl]-2-methyl-1,3-cyclohexadiene
1,3-CYCLOHEXADIENE, 5-((1S)-1,5-DIMETHYL-4-HEXEN-1-YL)-2-METHYL-, (5R)-
Microorganism:

Yes

IUPAC name(5R)-2-methyl-5-[(2S)-6-methylhept-5-en-2-yl]cyclohexa-1,3-diene
SMILESCC1=CCC(C=C1)C(C)CCC=C(C)C
InchiInChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8-10,14-15H,5,7,11H2,1-4H3/t14-,15+/m0/s1
FormulaC15H24
PubChem ID92776
Molweight204.35
LogP5.2
Atoms15
Bonds4
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10115
Supernatural-IDSN0188146-04

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaCandida AlbicansNAKarami et al. 2017
ProkaryotaEscherichia ColiNAKarami et al. 2017
ProkaryotaStaphylococcus AureusNAKarami et al. 2017
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaCandida AlbicansMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaEscherichia ColiMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaStaphylococcus AureusMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno


(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene

Compound Details

Synonymous names
(+)-delta-Cadinene
483-76-1
DELTA-CADINENE
(1S,8aR)-1-Isopropyl-4,7-dimethyl-1,2,3,5,6,8a-hexahydronaphthalene
D-Cadinene
(+)-D-Cadinene
CHEBI:15385
7848KI47OS
(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
.delta.-Cadinene, (+)-
delta-Amorphene
(1S,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthalene
(+)-?-Cadinene
UNII-7848KI47OS
(+)-??-Cadinene
(1S,8aR)-delta-cadinene
CADINENE, .DELTA.-
CHEMBL445759
FEMA NO. 4967
(+)-1(10),4-Cadinadiene
DTXSID70858792
MFCD02683434
AKOS016008860
LMPR0103330001
(+)-1S,8aR-Cadina-1(10),4-diene
1ST158489
DB-361881
C3734
NS00094789
C06394
F88000
Q27089406
NAPHTHALENE, DECAHYDRO-1,6-DIMETHYL-4- (1-METHYLETHYL)
(1S,8aR)-1-isopropyl-4,7-di-methyl-1,2,3,5,6,8a-hexahydronaphthalene
1,2,3,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)-(1S,8aR)-Naphthalene
Microorganism:

Yes

IUPAC name(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
SMILESCC1=CC2C(CCC(=C2CC1)C)C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13,15H,5-8H2,1-4H3/t13-,15-/m0/s1
FormulaC15H24
PubChem ID441005
Molweight204.35
LogP3.8
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID15385
Supernatural-IDSN0095604-05

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAspergillus FlavusITEM collection of CNR-ISPA (Research National Council of Italy - Institute of Sciences of Food Production) in Bari, ItalyJosselin et al. 2021
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
EukaryotaGanoderma Lucidumnasaprophytic on deciduous treesCampos Ziegenbein et al. 2006
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaAntrodia CinnamomeananaLu et al. 2014
EukaryotaAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaLaccaria BicolornanaDitengou et al. 2015
ProkaryotaStreptomyces Citreusn/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Caviscabiesn/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.n/aNADickschat et al. 2005_2
EukaryotaAspergillus UstusNAPolizzi et al. 2012
EukaryotaLaccaria Bicolorn/aNAMueller et al. 2013
EukaryotaPaxillus Involutusn/aNAMueller et al. 2013
EukaryotaArmillaria Mellean/aNAMueller et al. 2013
EukaryotaPholiota Squarrosan/aNAMueller et al. 2013
EukaryotaStropharia Rugosoannulatan/aNAMueller et al. 2013
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAspergillus FlavusSNA mediaSPME/GC-MSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
EukaryotaGanoderma LucidumnaGC/MSno
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaAntrodia CinnamomeaPDAGC/MSyes
EukaryotaAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
ProkaryotaStreptomyces Citreusn/an/ano
ProkaryotaStreptomyces Caviscabiesn/an/ano
ProkaryotaStreptomyces Sp.n/an/ano
EukaryotaAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS no
EukaryotaLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPaxillus InvolutusMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno


(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene

Compound Details

Synonymous names
ALPHA-CEDRENE
C09630
Cedrene
AC1L9CNB
alpha-cederene
DSSTox_CID_27032
DSSTox_RID_82053
CHEMBL3185669
CHEBI:173122
AKOS015951086
F82502
Q-200617
Q1956285
Microorganism:

Yes

IUPAC name(1S,2R,5S)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene
SMILESCC1CCC2C13CC=C(C(C3)C2(C)C)C
InchiInChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3/t11-,12?,13+,15+/m1/s1
FormulaC15H24
PubChem ID442348
Molweight204.35
LogP4.6
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10216
Supernatural-IDSN0153027-11

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaFusarium Oxysporum0NALi et al. 2018
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaFusarium OxysporumNALi et al. 2018
EukaryotaFusarium VerticillioidesNAUsseglio et al. 2017
EukaryotaMetschnikowia Reukaufiiinhibitory and promoting effects on the growth of different microorganismsisolate from Aconitum piepunense, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaDebaryomyces Hanseniiinhibitory and promoting effects on the growth of different microorganismsisolate from Silene acaulis, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaMrakia Blollopisinhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaTausonia Pullulansinhibitory and promoting effects on the growth of different microorganismsisolate from Silene acaulis, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaCystofilobasidium Sp.inhibitory and promoting effects on the growth of different microorganismsisolate from Silene acaulis, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaCystofilobasidium Capitatuminhibitory and promoting effects on the growth of different microorganismsisolate from Silene acaulis, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaGoffeauzyma Gilvescensinhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaRhodotorula Mucilaginosainhibitory and promoting effects on the growth of different microorganismsisolate from Dryas octopetala, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaSporidiobolus Salmonicolorinhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaCryptococcus Sp.inhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaVishniacozyma Victoriaeinhibitory and promoting effects on the growth of different microorganismsisolate from Dryas octopetala, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaMrakia Gelidainhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaCystobasidium Laryngisinhibitory and promoting effects on the growth of different microorganismsisolate from Cerasticum arcticum, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno
EukaryotaFusarium VerticillioidesCzapek-dox agarSPME, GC-MSyes
EukaryotaMetschnikowia Reukaufiiartificial nectar mediaGC-MSno
EukaryotaDebaryomyces Hanseniiartificial nectar mediaGC-MSno
EukaryotaMrakia Blollopisartificial nectar mediaGC-MSno
EukaryotaTausonia Pullulansartificial nectar mediaGC-MSno
EukaryotaCystofilobasidium Sp.artificial nectar mediaGC-MSno
EukaryotaCystofilobasidium Capitatumartificial nectar mediaGC-MSno
EukaryotaGoffeauzyma Gilvescensartificial nectar mediaGC-MSno
EukaryotaRhodotorula Mucilaginosaartificial nectar mediaGC-MSno
EukaryotaSporidiobolus Salmonicolorartificial nectar mediaGC-MSno
EukaryotaCryptococcus Sp.artificial nectar mediaGC-MSno
EukaryotaVishniacozyma Victoriaeartificial nectar mediaGC-MSno
EukaryotaMrakia Gelidaartificial nectar mediaGC-MSno
EukaryotaCystobasidium Laryngisartificial nectar mediaGC-MSno


(3R,4aS,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene

Compound Details

Synonymous names
BETA-SELINENE
(+)-beta-Selinene
beta-Eudesmene
17066-67-0
.beta.-Selinene
CHEBI:10443
Eudesma-4(14),11-diene
[4aR-(4aalpha,7alpha,8abeta)]-decahydro-4a-methyl-1-methylene-7-(1-methylethenyl)-naphthalene
(4aR,7R,8aS)-7-isopropenyl-4a-methyl-1-methylenedecahydronaphthalene
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethenyl)-, [4aR-(4a.alpha.,7.alpha.,8a.beta.)]-
.beta.-Eudesmene
(4aR,7R,8aS)-4a-methyl-1-methylidene-7-(prop-1-en-2-yl)-decahydronaphthalene
(4aR,7R,8aS)-4a-methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalene eudesma-4(14),11-diene
(+)-.beta.-Selinene
b-Selinene, (~90%)
C09723
CHEMBL2287242
YOVSPTNQHMDJAG-QLFBSQMISA-N
DTXSID201020829
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene-, (4aR-(4a.alpha.,7.alpha.,8a.beta.))-
LMPR0103190014
NS00113988
Q27108640
(4AR,7R,8aS)-4a-methyl-1-methylene-7-(prop-1-en-2-yl)decahydronaphthalene
(4aR,7R,8aS)-4a-methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalene
(4ar,7r,8as)-decahydro-4a-methyl-1-methylene-7-(1-methylethenyl)-naphthalene
Microorganism:

No

IUPAC name(3R,4aS,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene
SMILESCC(=C)C1CCC2(CCCC(=C)C2C1)C
InchiInChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h13-14H,1,3,5-10H2,2,4H3/t13-,14+,15-/m1/s1
FormulaC15H24
PubChem ID442393
Molweight204.35
LogP5.4
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10443
Supernatural-IDSN0456307-04

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAspergillus FlavusITEM collection of CNR-ISPA (Research National Council of Italy - Institute of Sciences of Food Production) in Bari, ItalyJosselin et al. 2021
EukaryotaPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaLaccaria BicolornanaDitengou et al. 2015
EukaryotaPhoma Sp.n/aNAStrobel et al. 2011
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAspergillus FlavusSNA mediaSPME/GC-MSno
EukaryotaPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
EukaryotaPhoma Sp.n/aSolid phase microextraction (SPME)no


(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene

Compound Details

Synonymous names
Thujopsene
(-)-Thujopsene
470-40-6
WIDDRENE
Thujopsene, (-)-
Sesquichamene
(-)-Thujopsen
cis-Thujopsene
E116U47P7N
(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene
cis-(-)-Thujopsene
Thujopsen
Cyclopropa(d)naphthalene, 1,1a,4,4a,5,6,7,8-octahydro-2,4a,8,8-tetramethyl-, (1aS,4aS,8aS)-
UNII-E116U47P7N
NSC-44707
(-)-widdrene
EINECS 207-426-8
NSC 44707
THUJOPSENE [MI]
CHEBI:9578
WXQGPFZDVCRBME-QEJZJMRPSA-N
Cyclopropa(D)Naphthalene, 1,1A,4,4A,5,6,7,8-Octahydro-2,4A,8,8-Tetramethyl-, (1As,4As,8As)
CYCLOPROPA(D)NAPHTHALENE, 1,1A,4,4A,5,6,7,8-OCTAHYDRO-2,4A,8,8-TETRAMETHYL-, (1AS-(1A.ALPHA.,4A.BETA.,8AR*))-
AKOS015914102
LMPR0103860001
(-)-Thujopsene, >=97.0% (GC)
C09740
A827133
Q15269711
(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,4a,5,6,7,8-octahydrocyclopropa[d]naphthalene
(1AS-(1aalpha,4abeta,8aR*))-1,1a,4,4a,5,6,7,8-octahydro-2,4a,8,8-tetramethylcyclopropa(d)naphthalene
Microorganism:

No

IUPAC name(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene
SMILESCC1=CCC2(CCCC(C23C1C3)(C)C)C
InchiInChI=1S/C15H24/c1-11-6-9-14(4)8-5-7-13(2,3)15(14)10-12(11)15/h6,12H,5,7-10H2,1-4H3/t12-,14-,15-/m0/s1
FormulaC15H24
PubChem ID442402
Molweight204.35
LogP4.8
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID9578
Supernatural-IDSN0422771-05

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaLaccaria Bicolorstimulates lateral root (LR) formation in Arabidopsis thaliana and Populus sp.naDitengou et al. 2015
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaXylaria Sp.naHaematoxylon brasiletto, Morelos, MexicoSánchez-Ortiz et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaXylaria Sp.PDA mediumSPME-GC/MSyes


3-(6-methylhept-5-en-2-yl)-6-methylidenecyclohexene

Mass-Spectra

Compound Details

Synonymous names
Sesquiphellandrene
3-(6-methylhept-5-en-2-yl)-6-methylidenecyclohexene
20307-83-9
3-(1,5-Dimethyl-4-hexenyl)-6-methylene-1-cyclohexene
UNII-T636HYS7CY
T636HYS7CY
Sesquiphellandrene, (-)-beta-
.beta.-Sesquiphellandrene
Cyclohexene, 3-(1,5-dimethyl-4-hexenyl)-6-methylene-, (S-(R*,S*))-
Cyclohexene, 3-(1,5-dimethyl-4-hexenyl)-6-methylene-, [S-(R*,S*)]-
(?)-?-Sesquiphellandrene
b-Sesquiphellandrene
beta-sesquiphellanderene
sesquiphellandrene (beta-)
3-((1S)-1,5-Dimethyl-4-hexenyl)-6-methylene-1-cyclohexene, (3R)-
DTXSID70864939
PHWISBHSBNDZDX-UHFFFAOYSA-N
DS-001018
NS00124356
3-(1,5-dimethyl-4-hexenyl)-6-methylene-cyclohexene
3-(1,5-Dimethyl-4-hexenyl)-6-methylenecyclohexene, 9CI
3-(6-METHYLHEPT-5-EN-2-YL)-6-METHYLIDENECYCLOHEX-1-ENE
Microorganism:

Yes

IUPAC name3-(6-methylhept-5-en-2-yl)-6-methylidenecyclohexene
SMILESCC(CCC=C(C)C)C1CCC(=C)C=C1
InchiInChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8,10,14-15H,3,5,7,9,11H2,1-2,4H3
FormulaC15H24
PubChem ID519764
Molweight204.35
LogP5.4
Atoms15
Bonds4
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID64361
Supernatural-IDSN0285867

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus CalidoustusNANAKoo et al. 2014
EukaryotaCandida AlbicansNAKarami et al. 2017
ProkaryotaEscherichia ColiNAKarami et al. 2017
EukaryotaAspergillus FischeriNADickschat et al. 2018
EukaryotaFusarium Oxysporum0NALi et al. 2018
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaFusarium OxysporumNALi et al. 2018
EukaryotaTrichoderma VirideNAMoisan et al. 2021
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
ProkaryotaBacillus AtrophaeusAgriculture University of Nanjing, ChinaTahir et al. 2017
ProkaryotaPseudomonas Fluorescensnafrom geo-authentic Atractylodes lanceaZhou et al. 2016
EukaryotaPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTrichoderma Atroviridenawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTrichoderma AtrovirideNAStoppacher et al. 2010
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus CalidoustusYPDTD/GC-MSno
EukaryotaCandida AlbicansMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaEscherichia ColiMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
EukaryotaAspergillus Fischerimedium 129CLSA-GCMSno
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno
EukaryotaTrichoderma Viride1/5th PDA mediumGC-MSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
ProkaryotaBacillus AtrophaeusLBSPME-GC-MSno
ProkaryotaPseudomonas FluorescensMS rooting agarGC/MS + comparison to NISTno
EukaryotaPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTrichoderma Atroviridemalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno


2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene

Mass-Spectra

Compound Details

Synonymous names
Cedrene
19069-48-8
2,6,6,8-TETRAMETHYLTRICYCLO[5.3.1.0(1,5)]UNDEC-8-ENE
68608-32-2
ALPHA-CEDRENE
Di-epi-.alpha.-cedrene
2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene
1H-3a,7-Methanoazulene, 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-
1H-3a,7-Methanoazulene, 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-, (3R,3aS,7S,8aS)-
1H-3a,7-Methanoazulene, 2,3,4,7,8,8a-hexahydro-3,6,8,8-tetramethyl-, [3R-(3.alpha.,3a.beta.,7.beta.,8a.alpha.)]-
Cedr-8-ene #
DTXSID00859378
CHEBI:167345
MCULE-9345089020
DB-025783
DB-051411
NS00012082
Microorganism:

Yes

IUPAC name2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene
SMILESCC1CCC2C13CC=C(C(C3)C2(C)C)C
InchiInChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h7,11-13H,5-6,8-9H2,1-4H3
FormulaC15H24
PubChem ID521207
Molweight204.35
LogP4.6
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID167345
Supernatural-IDSN0153027

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaMetschnikowia Reukaufiiinhibitory and promoting effects on the growth of different microorganismsisolate from Aconitum piepunense, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaGoffeauzyma Gilvescensinhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaRhodotorula Mucilaginosainhibitory and promoting effects on the growth of different microorganismsisolate from Dryas octopetala, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaSporidiobolus Salmonicolorinhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaCryptococcus Sp.inhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaVishniacozyma Victoriaeinhibitory and promoting effects on the growth of different microorganismsisolate from Dryas octopetala, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaMrakia Gelidainhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaPhoma Sp.n/aplant of L. tridentataStrobel et al. 2011
ProkaryotaStreptomyces ThermocarboxydusNANAPassari et al. 2019
Fusarium GraminearumBallot et al. 2023
Kluyveromyces MarxianusJi et al. 2024
Saccharomyces CerevisiaeJi et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaMetschnikowia Reukaufiiartificial nectar mediaGC-MSno
EukaryotaGoffeauzyma Gilvescensartificial nectar mediaGC-MSno
EukaryotaRhodotorula Mucilaginosaartificial nectar mediaGC-MSno
EukaryotaSporidiobolus Salmonicolorartificial nectar mediaGC-MSno
EukaryotaCryptococcus Sp.artificial nectar mediaGC-MSno
EukaryotaVishniacozyma Victoriaeartificial nectar mediaGC-MSno
EukaryotaMrakia Gelidaartificial nectar mediaGC-MSno
EukaryotaPhoma Sp.n/aSolid phase microextraction (SPME)no
ProkaryotaStreptomyces Thermocarboxydusactinomycetes isolation agar (AIA)GC-MSno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno
Kluyveromyces MarxianusSauce Meat during StorageSPME–GC–MSno
Saccharomyces CerevisiaeSauce Meat during StorageSPME–GC–MSno


8a-methyl-4-methylidene-6-propan-2-ylidene-2,3,4a,5,7,8-hexahydro-1H-naphthalene

Mass-Spectra

Compound Details

Synonymous names
gamma-Selinene
Eudesma-4(14),7(11)-diene
Eudesma-4(15),7(11)-diene
Selina-4(14),7(11)-diene
g-Selinene
(4aR,8aS)-4a-Methyl-1-methylene-7-(propan-2-ylidene)decahydronaphthalene
4(15),7(11)-Selinadiene
CHEBI:167347
RMZHSBMIZBMVMN-UHFFFAOYSA-N
8a-methyl-4-methylidene-6-propan-2-ylidene-2,3,4a,5,7,8-hexahydro-1H-naphthalene
4a-methyl-1-methylidene-7-(propan-2-ylidene)-decahydronaphthalene
decahydro-4a-methyl-1-methylene-7-(1-methylethylidene) naphthalene
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethylidene)-, (4aR,8aS)-
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethylidene)-, trans-
Microorganism:

No

IUPAC name8a-methyl-4-methylidene-6-propan-2-ylidene-2,3,4a,5,7,8-hexahydro-1H-naphthalene
SMILESCC(=C1CCC2(CCCC(=C)C2C1)C)C
InchiInChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h14H,3,5-10H2,1-2,4H3
FormulaC15H24
PubChem ID521334
Molweight204.35
LogP4.7
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID167347
Supernatural-IDSN0329816

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaPleurotus EryngiinanaUsami et al. 2014
EukaryotaLaccaria BicolornanaDitengou et al. 2015
EukaryotaTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaPleurotus EryngiinaGC/MS, GC-O, AEDAno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no


(1S,4S,7R)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulene

Compound Details

Synonymous names
alpha-Guaiene
3691-12-1
Guaia-1(5),11-diene
DTXSID5052046
CHEBI:63443
(1S,4S,7R)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulene
(1S,4S,7R)-1,4-dimethyl-7-(prop-1-en-2-yl)-1,2,3,4,5,6,7,8-octahydroazulene
alpha-guaiene,guaia-1(5),11-diene,[1S-(1a,4a,7a)]-1,2,3,4,5,6,7,8-octahydro-1,4-dimethyl-7-(1-methylethenyl)-azulene
Azulene, 1,2,3,4,5,6,7,8-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, [1S-(1.alpha.,4.alpha.,7.alpha.)]-
ABQ2CB7VAC
Azulene, 1,2,3,4,5,6,7,8-octahydro-1,4-dimethyl-7-(1-methylethenyl)-, (1S,4S,7R)-
a-Guaiene (>85%)
DTXCID0030613
7-Isopropenyl-1,4-dimethyl-1,2,3,4,5,6,7,8-octahydroazulene-, [1S-(1.alpha.,4.alpha.,7.alpha.)]-
C20161
Q5613309
Microorganism:

No

IUPAC name(1S,4S,7R)-1,4-dimethyl-7-prop-1-en-2-yl-1,2,3,4,5,6,7,8-octahydroazulene
SMILESCC1CCC(CC2=C1CCC2C)C(=C)C
InchiInChI=1S/C15H24/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h11-13H,1,5-9H2,2-4H3/t11-,12-,13+/m0/s1
FormulaC15H24
PubChem ID5317844
Molweight204.35
LogP4.6
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID63443
Supernatural-IDSN0002560-02

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaHypoxylon AnthochroumNAMacías-Rubalcava et al. 2018
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaHypoxylon Anthochroumnaendophytic in Bursera lancifoliaUlloa-Benítez et al. 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaHypoxylon Anthochroumrice medium (RM, 300g of rice and 300ml of water)SPME, GC-MSyes
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaHypoxylon AnthochroumPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSno


1-methyl-4-(6-methylhept-5-en-2-yl)cyclohexa-1,4-diene

Compound Details

Synonymous names
beta-Curcumene
.beta.-curcumene
1-methyl-4-(6-methylhept-5-en-2-yl)cyclohexa-1,4-diene
CHEBI:62759
DTXSID001197513
72345-84-7
Q27132149
1-(1,5-dimethyl-4-hexenyl)-4-methyl-1,4-cyclohexadiene
1-(1,5-Dimethyl-4-hexen-1-yl)-4-methyl-1,4-cyclohexadiene
1-(1,5-dimethyl-hex-4-enyl)-4-methyl-cyclohexa-1,4-diene
Microorganism:

No

IUPAC name1-methyl-4-(6-methylhept-5-en-2-yl)cyclohexa-1,4-diene
SMILESCC1=CCC(=CC1)C(C)CCC=C(C)C
InchiInChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8,11,14H,5,7,9-10H2,1-4H3
FormulaC15H24
PubChem ID6428461
Molweight204.35
LogP4.7
Atoms15
Bonds4
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID62760
Supernatural-IDSN0178355

mVOC Specific Details


Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(3R,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene

Compound Details

Synonymous names
Valencene
(+)-Valencene
4630-07-3
Valencen
(3R,4aS,5R)-4a,5-dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene
FEMA No. 3443
DTXSID8047052
CHEBI:61700
96H21P91IG
Valencene (natural)
ent-7betaH-eremophila-10(1),11-diene
(+)-Valencene 1000 microg/mL in Isopropanol
(1R-(1alpha,7beta,8alpha))-1,2,3,5,6,7,8,8a-Octahydro-1,8a-dimethyl-7-(1-methylvinyl)naphthalene
Naphthalene, 1,2,3,5,6,7,8,8a-octahydro-1,8a-dimethyl-7-(1-methylethenyl)-, (1R,7R,8aS)-
NSC-148969
(3R,4aS,5R)-4a,5-Dimethyl-3-isopropenyl-1,2,3,4,4a,5,6,7-octahydronaphthalene
(A+/-)-valencene
4.beta.H,5.alpha.-Eremophila-1(10),11-diene
VALENCENE [FHFI]
VALENCENE [INCI]
(+)-Valencene, tech grade
Valencene (Technical Grade)
UNII-96H21P91IG
Valencene, natural, >=65%
CHEMBL3186909
DTXCID6027052
(+)-Valencene, analytical standard
HY-N6636
NAPHTHALENE, 1,2,3,5,6,7,8,8A-OCTAHYDRO-1,8A-DIMETHYL-7-(1-METHYLETHENYL)-, (1R-(1.ALPHA.,7.BETA.,8A.ALPHA.))-
EINECS 225-047-6
Tox21_302397
MFCD00075884
(+)-Valencene, technical, >=70%
AKOS027460688
NSC 148969
NCGC00256249-01
MS-23110
CAS-4630-07-3
4Betah,5alpha-eremophila-1(10),11-diene
CS-0044199
C17277
F71379
Q289496
4alpha,10alpha-Dimethyl-6beta-isopropyl-delta1,9-octalin
4alpha,10alpha-Dimethyl-6beta-isopropyl-.DELTA.1,9-octalin
(3R,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene
1,2,3,5,6,7,8,8a-Octahydro-1,8A-dimethyl-7-(1-methylethenyl)naphthalene, (1R-(1alpha,7beta,8aalpha))-
Naphthalene, 1,2,3,5,6,7,8,8A-octahydro-1,8A-dimethyl-7-(1-methylethenyl)-, (1R-(1alpha,7beta,8aalpha))-
Microorganism:

Yes

IUPAC name(3R,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene
SMILESCC1CCC=C2C1(CC(CC2)C(=C)C)C
InchiInChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h7,12-13H,1,5-6,8-10H2,2-4H3/t12-,13-,15+/m1/s1
FormulaC15H24
PubChem ID9855795
Molweight204.35
LogP5.2
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID61700
Supernatural-IDSN0302870-06

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaHypoxylon AnthochroumNAMacías-Rubalcava et al. 2018
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
ProkaryotaStreptomyces Salmoniscontrol of postharvest anthracnose disease of chili caused by Colletotrichum gloeosporioides PSU-03Phitsanulok Seed Research and Development Center, Department of Agriculture, Ministry of Agriculture and Cooperatives, ThailanBoukaew et al. 2021
EukaryotaPenicillium Roquefortin/aobtained fronm department of Biotechnology , Denmark Technical Universität at CopenhagenJelen 2003
EukaryotaMuscodor Albusn/aobtained from limbs of vineAtmosukarto et al. 2005
EukaryotaMuscodor Fengyangensisn/aZhejiang Province of Southeast ChinaZhang et al. 2010
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
EukaryotaPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaHypoxylon Anthochroumrice medium (RM, 300g of rice and 300ml of water)SPME, GC-MSyes
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
ProkaryotaStreptomyces SalmonisGYM agarSPME/GC-MSno
EukaryotaPenicillium Roqueforti wheat kernel mediumincubated at 20°C for 14 days, isolation by SPME with different fibresno
EukaryotaMuscodor AlbusPotato dextrose agar (PDA)SPME - GC - MS - culture 12 days oldno
EukaryotaMuscodor Fengyangensispotato dextrose agarThe MVOCs emitted by the mycelia of Muscodor were investigated by Solid phase microextraction/Gas chromatograph/Mass spectra (SPME/GC/MS). no
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


(4S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohexene

Mass-Spectra

Compound Details

Synonymous names
beta-Bisabolene
495-61-4
(S)-beta-bisabolene
(-)-beta-bisabolene
l-beta-Bisabolene
(S)-1-Methyl-4-(5-methyl-1-methylene-4-hexenyl)cyclohexene
.beta.-Bisabolene
(S)-1-Methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene
(-)-.beta.-bisabolene
S19BRC22QA
CHEBI:49263
Cyclohexene, 1-methyl-4-(5-methyl-1-methylene-4-hexenyl)-, (S)-
(4S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohexene
(S)-(-)-6-methyl-2-(4-methyl-3-cyclohexen-1-yl)-1,5-heptadiene
6-methyl-2-[(1R)-4-methyl-1-cyclohex-3-enyl]hepta-1,5-diene
1,5-Heptadiene, 6-methyl-2-(4-methyl-3-cyclohexen-1-yl)-, (S)-(-)-
(1S)-bisabola-4,7(11),10(15)-triene (4S)-1-methyl-4-(5-methyl-1-methylenehex-4-en-1-yl)cyclohexene
UNII-S19BRC22QA
??-Bisabolene
l-.beta.-Bisabolene
BISABOLENE [FHFI]
(+,-)-.beta.-Bisabolene
CHEMBL1077088
FEMA NO. 4940
(-)-b-Bisabolene (>85%)
(-)-beta-Bisabolene (>85%)
DTXSID701017550
Cyclohexene, 1-methyl-4-(5-methyl-1-methylene-4-hexenyl)-, (4S)-
AKOS040758160
LMPR0103060013
BS-47085
HY-136552
CS-0131096
(1S)-bisabola-4,7(11),10(15)-triene
F73181
Q11595687
(s)-1-methyl-4-(5-methyl-1-methylene-4-hexenyl)-cyclohexene
1-Methyl-4-(5-methyl-1-methylene-4-hexenyl)-(S)-cyclohexene
(4S)-1-methyl-4-(5-methyl-1-methylenehex-4-en-1-yl)cyclohexene
(4S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohex-1-ene
1-Methyl-4-(5-methyl-1-methylene-4-hexenyl)-1-cyclohexene-, (4S)-
CYCLOHEXENE, 1-METHYL-4-(5-METHYL-1-METHYLENE-4-HEXENYL-(S)-
CYCLOHEXENE, 1-METHYL-4-(5-METHYL-1-METHYLENE-4-HEXEN-1-YL)-, (4S)-
Microorganism:

Yes

IUPAC name(4S)-1-methyl-4-(6-methylhepta-1,5-dien-2-yl)cyclohexene
SMILESCC1=CCC(CC1)C(=C)CCC=C(C)C
InchiInChI=1S/C15H24/c1-12(2)6-5-7-14(4)15-10-8-13(3)9-11-15/h6,8,15H,4-5,7,9-11H2,1-3H3/t15-/m1/s1
FormulaC15H24
PubChem ID10104370
Molweight204.35
LogP5.2
Atoms15
Bonds4
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID49263
Supernatural-IDSN0444416-02

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAHeddergott et al. 2014
EukaryotaAspergillus ClavatusNADickschat et al. 2018
EukaryotaAspergillus FischeriNADickschat et al. 2018
EukaryotaFusarium Oxysporum0NALi et al. 2018
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaFusarium OxysporumNALi et al. 2018
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
EukaryotaPleurotus CystidiosusnanaUsami et al. 2014
EukaryotaTrichoderma Harzianumn/aNAZhang et al. 2014
EukaryotaTrichoderma AtrovirideNAStoppacher et al. 2010
EukaryotaLaccaria Bicolorn/aNAMueller et al. 2013
EukaryotaPaxillus Involutusn/aNAMueller et al. 2013
EukaryotaArmillaria Mellean/aNAMueller et al. 2013
EukaryotaPholiota Squarrosan/aNAMueller et al. 2013
EukaryotaStropharia Rugosoannulatan/aNAMueller et al. 2013
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
EukaryotaGanoderma Lucidumnasaprophytic on deciduous treesCampos Ziegenbein et al. 2006
EukaryotaPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTrichoderma Atroviridenawater damaged buildings, BelgiumPolizzi et al. 2012
ProkaryotaLentilactobacillus BuchneriNANASquara et al. 2022
ProkaryotaLacticaseibacillus ParacaseiNANASquara et al. 2022
Kluyveromyces MarxianusJi et al. 2024
Saccharomyces CerevisiaeJi et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusBrianSPME/GC-MSno
EukaryotaAspergillus Clavatusmedium 129CLSA-GCMSno
EukaryotaAspergillus Fischerimedium 129CLSA-GCMSno
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
EukaryotaPleurotus CystidiosusnaGC/MS, GC-O, AEDAno
EukaryotaTrichoderma HarzianumMinimal mediaSPME/GC-MSno
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPaxillus InvolutusMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaGanoderma LucidumnaGC/MSno
EukaryotaPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTrichoderma Atroviridemalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
Kluyveromyces MarxianusSauce Meat during StorageSPME–GC–MSno
Saccharomyces CerevisiaeSauce Meat during StorageSPME–GC–MSno


(1S,4S,5S,9R)-1,8-dimethyl-4-propan-2-ylspiro[4.5]dec-7-en-9-ol

Compound Details

Synonymous names
SCHEMBL20199944
Microorganism:

No

IUPAC name(1S,4S,5S,9R)-1,8-dimethyl-4-propan-2-ylspiro[4.5]dec-7-en-9-ol
SMILESCC1CCC(C12CC=C(C(C2)O)C)C(C)C
InchiInChI=1S/C15H26O/c1-10(2)13-6-5-12(4)15(13)8-7-11(3)14(16)9-15/h7,10,12-14,16H,5-6,8-9H2,1-4H3/t12-,13-,14+,15-/m0/s1
FormulaC15H26O
PubChem ID10331156
Molweight222.37
LogP3.9
Atoms16
Bonds1
H-bond Acceptor1
H-bond Donor1
Chemical Classificationterpenes
Supernatural-IDSN0406103-04

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno


(3R,4aR,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene

Compound Details

Synonymous names
ALPHA-SELINENE
473-13-2
Eudesma-3,11-diene
alpha-Selinine
UNII-99ZHA8F274
99ZHA8F274
SELINA-3,11-DIENE
(2R,4aR,8aR)-4a,8-dimethyl-2-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
(2R-(2alpha,4aalpha,8abeta))-1,2,3,4,4a,5,6,8a-Octahydro-4a,8-dimethyl-2-(1-methylethenyl)naphthalene
CHEBI:59961
(3R,4aR,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-4a,8-dimethyl-2-(1-methylethenyl)-, (2R-(2alpha,4aalpha,8abeta))-
(-)-alpha-Selinene
alpha-celinene
Selina-4,11-diene
a-Selinine, >85%
alpha-SELINENE, (-)-
(-)-.ALPHA.-SELINENE
DTXSID50963792
.ALPHA.-SELINENE, (-)-
XS174882
C22044
Q7448480
(2R-(2.ALPHA.,4A.ALPHA.,8A.BETA.))-1,2,3,4,4A,5,6,8A-OCTAHYDRO-4A,8-DIMETHYL-2-(1-METHYLETHENYL)NAPHTHALENE
NAPHTHALENE, 1,2,3,4,4A,5,6,8A-OCTAHYDRO-4A,8-DIMETHYL-2-(1-METHYLETHENYL)-, (2R,4AR,8AR)-
Microorganism:

No

IUPAC name(3R,4aR,8aR)-5,8a-dimethyl-3-prop-1-en-2-yl-2,3,4,4a,7,8-hexahydro-1H-naphthalene
SMILESCC1=CCCC2(C1CC(CC2)C(=C)C)C
InchiInChI=1S/C15H24/c1-11(2)13-7-9-15(4)8-5-6-12(3)14(15)10-13/h6,13-14H,1,5,7-10H2,2-4H3/t13-,14+,15-/m1/s1
FormulaC15H24
PubChem ID10856614
Molweight204.35
LogP5.2
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID59961
Supernatural-IDSN0279450-03

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAspergillus FlavusITEM collection of CNR-ISPA (Research National Council of Italy - Institute of Sciences of Food Production) in Bari, ItalyJosselin et al. 2021
EukaryotaPenicillium Roquefortin/aobtained fronm department of Biotechnology , Denmark Technical Universität at CopenhagenJelen 2003
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaAntrodia CinnamomeananaLu et al. 2014
EukaryotaPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAspergillus FlavusSNA mediaSPME/GC-MSno
EukaryotaPenicillium Roqueforti wheat kernel mediumincubated at 20°C for 14 days, isolation by SPME with different fibresno
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaAntrodia CinnamomeaPDAGC/MSyes
EukaryotaPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


(4aR)-3,5,5,9-tetramethyl-1,2,4a,6,7,8-hexahydrobenzo[7]annulene

Compound Details

Synonymous names
beta-Himachalene
1461-03-6
Himachalene
.beta.-Himachalene
(R)-beta-himachalene
(+)-.beta.-Himachalene
himachal-1(11),4-diene
F8Y2422O3M
(4aR)-3,5,5,9-tetramethyl-1,2,4a,6,7,8-hexahydrobenzo[7]annulene
(R)-2,4a,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-1H-benzocycloheptene
(R)-3,5,5,9-Tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene
(+)-2,4abeta,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-1H-benzocycloheptene
(4aR)-3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene
1H-Benzocycloheptene, 2,4a.beta.,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-, (+)-
1H-Benzocycloheptene, 2,4a,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-, (R)-
UNII-F8Y2422O3M
CHEBI:49208
LCOSCMLXPAQCLQ-AWEZNQCLSA-N
.BETA.-HIMACHALENE, (+)-
1H-Benzocycloheptene, 2,4abeta,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-, (+)-
Q27121532
1H-BENZOCYCLOHEPTENE, 2,4A,5,6,7,8-HEXAHYDRO-3,5,5,9-TETRAMETHYL-, (4AR)
1H-Benzocycloheptene, 2,4a,5,6,7,8-hexahydro-3,5,5,9-tetramethyl-, (4aR)-
3,5,5,9-Tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[a]cycloheptene-, (R)-
Microorganism:

No

IUPAC name(4aR)-3,5,5,9-tetramethyl-1,2,4a,6,7,8-hexahydrobenzo[7]annulene
SMILESCC1=CC2C(=C(CCCC2(C)C)C)CC1
InchiInChI=1S/C15H24/c1-11-7-8-13-12(2)6-5-9-15(3,4)14(13)10-11/h10,14H,5-9H2,1-4H3/t14-/m0/s1
FormulaC15H24
PubChem ID11586487
Molweight204.35
LogP3.9
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID49208
Supernatural-IDSN0201839-01

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FumigatusNANAAhmed et al. 2018
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAspergillus FlavusITEM collection of CNR-ISPA (Research National Council of Italy - Institute of Sciences of Food Production) in Bari, ItalyJosselin et al. 2021
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTrichoderma Viriden/aNAHung et al. 2013
EukaryotaPhoma Sp.n/aNAStrobel et al. 2011
EukaryotaTrichoderma VirensNACrutcher et al. 2013
EukaryotaTrichoderma AtrovirideNACrutcher et al. 2013
EukaryotaTrichoderma ReeseiNACrutcher et al. 2013
EukaryotaTuber Magnatumn/aItalian geographical areas ( Umbria)Gioacchini et al. 2008
EukaryotaLaccaria Bicolorn/aNAMueller et al. 2013
EukaryotaPaxillus Involutusn/aNAMueller et al. 2013
EukaryotaArmillaria Mellean/aNAMueller et al. 2013
EukaryotaPholiota Squarrosan/aNAMueller et al. 2013
EukaryotaStropharia Rugosoannulatan/aNAMueller et al. 2013
EukaryotaTrichoderma Viriden/aNAMueller et al. 2013
Fusarium GraminearumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus FumigatusAMMTD/GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAspergillus FlavusSNA mediaSPME/GC-MSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTrichoderma VirideMalt extract agar Headspace volatiles collected with colomn/TD-GC-MSno
EukaryotaPhoma Sp.n/aSolid phase microextraction (SPME)no
EukaryotaTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma ReeseiPotato dextrose agarHS-SPME/GC-MS no
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPaxillus InvolutusMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(1S,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene

Compound Details

Synonymous names
gamma-Muurolene
(+)-gamma-muurolene
CHEBI:64798
DTXSID401017737
(1S,4aS,8aR)-1-isopropyl-7-methyl-4-methylene-1,2,3,4,4a,5,6,8a-octahydronaphthalene
(1S,4aS,8aR)-7-methyl-4-methylene-1-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
(1S,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
DTXCID701475932
C20273
Q27133437
Microorganism:

Yes

IUPAC name(1S,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
SMILESCC1=CC2C(CC1)C(=C)CCC2C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13-15H,4-8H2,1-3H3/t13-,14+,15-/m0/s1
FormulaC15H24
PubChem ID12313020
Molweight204.35
LogP4.3
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID64798
Supernatural-IDSN0417892-09

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaTrichoderma HamatumNAGuo et al. 2019
EukaryotaTrichoderma HarzianumNAGuo et al. 2019
EukaryotaTrichoderma VirensNAGuo et al. 2019
EukaryotaAspergillus FlavusITEM collection of CNR-ISPA (Research National Council of Italy - Institute of Sciences of Food Production) in Bari, ItalyJosselin et al. 2021
EukaryotaTrichoderma Asperellumreduce downy mildew severity on Vitis vinifera (grapevine plants)Cotxarrera et al., 2002Lazazzara et al. 2021
EukaryotaTrichoderma Atroviridereduce downy mildew severity on Vitis vinifera (grapevine plants)Pertot et al., 2008Lazazzara et al. 2021
EukaryotaTrichoderma Harzianumreduce downy mildew severity on Vitis vinifera (grapevine plants)Eladet al., 1997Lazazzara et al. 2021
ProkaryotaStreptomyces GriseusNARiu et al. 2022
EukaryotaFusarium Culmorumnasandy dune soil, NetherlandsSchmidt et al. 2015
ProkaryotaStreptomyces Caviscabiesn/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.n/aNADickschat et al. 2005_2
EukaryotaTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al. 2008
EukaryotaArmillaria Mellean/aNAMueller et al. 2013
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaAntrodia CinnamomeananaLu et al. 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaTrichoderma HamatumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma HarzianumMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaTrichoderma VirensMelin-Norkrans synthetic mediumSBSE-GC-MSno
EukaryotaAspergillus FlavusSNA mediaSPME/GC-MSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
ProkaryotaStreptomyces GriseusTSA mediaSPME/GC-MSno
EukaryotaFusarium Culmorumpotato dextrose agarGC/MS-Q-TOFno
ProkaryotaStreptomyces Caviscabiesn/an/ano
ProkaryotaStreptomyces Sp.n/an/ano
EukaryotaTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)no
EukaryotaArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaAntrodia CinnamomeaPDAGC/MSyes