Results for:
Species: Penicillium decumbens

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

Compound Details

Synonymous names
.beta.-Acoradiene
Microorganism:

No

IUPAC name(1S,4R,5R)-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-/m0/s1
FormulaC15H24
PubChem ID6428280
Molweight204.35
LogP5.1
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID172925
Supernatural-IDSN0076261-08

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFusarium OxysporumNAWeikl et al. 2016
EukaryotaPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Fusarium GraminearumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFusarium OxysporumSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,9-diene

Compound Details

Synonymous names
alpha-Chamigrene
19912-83-5
C09635
(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,9-diene
AC1L9CNK
CHEBI:10220
(6R)-3,7,11,11-tetramethylspiro[5.5]undeca-3,7-diene
DTXSID40331805
SPIRO[5.5]UNDECA-1,8-DIENE,1,
Q27108602
Microorganism:

No

IUPAC name(6R)-1,5,5,9-tetramethylspiro[5.5]undeca-1,9-diene
SMILESCC1=CCC2(CC1)C(=CCCC2(C)C)C
InchiInChI=1S/C15H24/c1-12-7-10-15(11-8-12)13(2)6-5-9-14(15,3)4/h6-7H,5,8-11H2,1-4H3/t15-/m1/s1
FormulaC15H24
PubChem ID442351
Molweight204.35
LogP4.4
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10220
Supernatural-IDSN0346089-02

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaXylaria Sp.naHaematoxylon brasiletto, Morelos, MexicoSánchez-Ortiz et al. 2016
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Roquefortin/aobtained fronm department of Biotechnology , Denmark Technical Universität at CopenhagenJelen 2003
Fusarium GraminearumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaXylaria Sp.PDA mediumSPME-GC/MSyes
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Roqueforti wheat kernel mediumincubated at 20°C for 14 days, isolation by SPME with different fibresno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(6R)-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-ene

Compound Details

Synonymous names
(-)-beta-Chamigrene
beta-Chamigrene
18431-82-8
(-)-chamigrene
(R)-beta-chamigrene
Chamigrene
Chamigren
(6R)-3,7,7-trimethyl-11-methylidenespiro[5.5]undec-2-ene
(6R)-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-ene
CHEBI:10359
(R)-11-Methylene-3,7,7-trimethylspiro[5.5]undec-2-ene
DTXSID60939822
WLNGPDPILFYWKF-OAHLLOKOSA-N
C09637
Q27108622
Microorganism:

No

IUPAC name(6R)-5,5,9-trimethyl-1-methylidenespiro[5.5]undec-9-ene
SMILESCC1=CCC2(CC1)C(=C)CCCC2(C)C
InchiInChI=1S/C15H24/c1-12-7-10-15(11-8-12)13(2)6-5-9-14(15,3)4/h7H,2,5-6,8-11H2,1,3-4H3/t15-/m1/s1
FormulaC15H24
PubChem ID442353
Molweight204.35
LogP4.7
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10359
Supernatural-IDSN0413520-02

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus CalidoustusNANAKoo et al. 2014
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaPhoma Sp.n/aNAStrobel et al. 2011
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Fusarium GraminearumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus CalidoustusYPDTD/GC-MSno
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaPhoma Sp.n/aSolid phase microextraction (SPME)no
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(6E)-7,11-dimethyl-3-methylidenedodeca-1,6,10-triene

Mass-Spectra

Compound Details

Synonymous names
18794-84-8
trans-beta-Farnesene
(E)-beta-farnesene
BETA-FARNESENE
(E)-7,11-Dimethyl-3-methylenedodeca-1,6,10-triene
7,11-Dimethyl-3-methylenedodeca-1,6,10-triene
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-, (6E)-
b-farnesene
(6E)-7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
trans-B-farnesene
.beta.-Farnesene
77129-48-7
trans-7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
beta-trans-farnesene
(E)-|A-Farnesene
(6E)-7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-, (E)-
EINECS 278-628-1
E5STW643HU
(6E)-7,11-dimethyl-3-methylene-dodeca-1,6,10-triene
DTXSID9047049
MFCD00065433
(E)-.beta.-Farnesene
7,11-Dimethyl-3-methylene-1,6E,10-dodecatriene
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
UNII-E5STW643HU
trans--Farnesene
b-trans-Farnesene
(e)-b-Farnesene
I(2)-farnesene
EINECS 242-582-0
(6E)-beta-farnesene
trans- beta -Farnesene
(Z,E)-.beta.-Farnesene
EC 242-582-0
FARNESENE, .BETA.-
FARNESENE, TRANS-BETA-
TRANS-.BETA.-FARNESENE
QSPL 026
.BETA.-FARNESENE [MI]
DTXCID7027049
FEMA NO. 4971
CHEBI:10418
CHEBI:39241
JSNRRGGBADWTMC-UHFFFAOYSA-N
HY-N7364
.BETA.-FARNESENE, (6E)-
Tox21_303792
LMFA11000040
AKOS015913412
NCGC00357080-01
trans-beta-Farnesene, analytical standard
BS-53181
CAS-18794-84-8
CS-0113875
FEMA NO. 3839, (6E)-.BETA.-
C09666
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-
Q27108631
(6E)-7,11-dimethyl-3-methylenedodeca-1,6,10-triene
(E)-7,11-dimethyl-3-methylene-dodeca-1,6,10-triene
(E)-7,11-DIMETHYL-3-METHYLENE-1,6,10-DODECATRIENE
TRANS-.BETA.-FARNESENE (CONSTITUENT OF CHAMOMILE) [DSC]
1207091-65-3
Microorganism:

Yes

IUPAC name(6E)-7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
SMILESCC(=CCCC(=CCCC(=C)C=C)C)C
InchiInChI=1S/C15H24/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12H,1,4,7-8,10-11H2,2-3,5H3/b15-12+
FormulaC15H24
PubChem ID5281517
Molweight204.35
LogP6.2
Atoms15
Bonds7
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID10418
Supernatural-IDSN0174069-01

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFusarium Oxysporum0NALi et al. 2018
EukaryotaCandida AlbicansATCC MYA-2876, American Type Culture CollectionCosta et al. 2020
EukaryotaCandida GlabrataATCC 90030, American Type Culture CollectionCosta et al. 2020
EukaryotaCandida TropicalisATCC 750, American Type Culture CollectionCosta et al. 2020
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
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
EukaryotaGanoderma Lucidumnasaprophytic on deciduous treesCampos Ziegenbein et al. 2006
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaTrichoderma AtrovirideNAStoppacher et al. 2010
EukaryotaAspergillus Fumigatuscompost Fischer et al. 1999
EukaryotaTrichoderma VirensNACrutcher et al. 2013
EukaryotaTrichoderma AtrovirideNACrutcher et al. 2013
EukaryotaTrichoderma ReeseiNACrutcher et al. 2013
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
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaCandida AlbicansYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida GlabrataYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida TropicalisYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaTrichoderma AsperellumPDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma AtroviridePDA mediaHS-SPME/GC-MSno
EukaryotaTrichoderma HarzianumPDA mediaHS-SPME/GC-MSno
EukaryotaDebaryomyces Hanseniiartificial nectar mediaGC-MSno
EukaryotaGanoderma LucidumnaGC/MSno
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaAspergillus Fumigatusyest extract sucroseTenax/GC-MSno
EukaryotaTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma ReeseiPotato 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


(1R,2R,6S)-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undec-8-ene

Compound Details

Synonymous names
.alpha.-Barbatene
RMKQBFUAKZOVPQ-JALIKCBVSA-N
DTXSID201344194
C19740
Microorganism:

No

IUPAC name(1R,2R,6S)-1,2,6,8-tetramethyltricyclo[5.3.1.02,6]undec-8-ene
SMILESCC1=CCC2(CC1C3(C2(CCC3)C)C)C
InchiInChI=1S/C15H24/c1-11-6-9-13(2)10-12(11)14(3)7-5-8-15(13,14)4/h6,12H,5,7-10H2,1-4H3/t12?,13-,14+,15-/m1/s1
FormulaC15H24
PubChem ID6427471
Molweight204.35
LogP4.8
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


(1S,2S,4R)-1-ethenyl-1-methyl-2,4-bis(prop-1-en-2-yl)cyclohexane

Compound Details

Synonymous names
BETA-ELEMENE
515-13-9
(-)-beta-Elemene
beta-Elemen
Levo-beta-elemene
(1S,2S,4R)-1-methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane
Elemene
2,4-Diisopropenyl-1-methyl-1-vinylcyclohexane
b-elemene
beta-Elemene, (-)-
CHEBI:62855
Levo-b-elemene
UNII-2QG8CX6LXD
2QG8CX6LXD
(-)-b-Elemene
(1S,2S,4R)-1-ethenyl-1-methyl-2,4-bis(prop-1-en-2-yl)cyclohexane
33880-83-0
(1S,2S,4R)-2,4-diisopropenyl-1-methyl-1-vinylcyclohexane
(1S,2S,4R)-(-)-1-methyl-1-vinyl-2,4-diisopropenylcyclohexane
ELEMENE, (-)-BETA-
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S,2S,4R)-
(+/-)-beta-Elemene
(1S,2S,4R)-1-ethenyl-1-methyl-2,4-di(prop-1-en-2-yl)cyclohexane
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S-(1-alpha,2-beta,4-beta))-
.beta.-Elemene
1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-cyclohexane
Cyclohexane, 2,4-diisopropenyl-1-methyl-1-vinyl-, (1S,2S,4R)-
EINECS 251-713-0
(-)-.beta.-Elemene
b-Elemen
(-)-bete-elemene
E- .beta.-Elemene
Beta elemene [WHO-DD]
Epitope ID:153551
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-
(1S,2S,4R)-beta-elemene
Levo-b-elemene(-)-b-Elemene
CHEMBL448502
CHEBI:62854
DTXSID40865690
DTXSID60881211
SDP-111
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1alpha,2beta,4beta)-
OPFTUNCRGUEPRZ-QLFBSQMISA-N
?-Elemene (10mg/ml in ethanol)
ELEMENE, (-)-.BETA.-
s6957
AKOS028108977
(-)-beta-Elemene, analytical standard
AS-82909
HY-107324
CS-0028143
NS00096333
C17094
E79113
EN300-1709739
Q27132237
rel-(1S,2S,4R)-1-ethenyl-1-methyl-2,4-di(prop-1-en-2-yl)cyclohexane
rel-(1S,2S,4R)-1-methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane
(1alpha,2beta,4beta)-1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)cyclohexane
Microorganism:

Yes

IUPAC name(1S,2S,4R)-1-ethenyl-1-methyl-2,4-bis(prop-1-en-2-yl)cyclohexane
SMILESCC(=C)C1CCC(C(C1)C(=C)C)(C)C=C
InchiInChI=1S/C15H24/c1-7-15(6)9-8-13(11(2)3)10-14(15)12(4)5/h7,13-14H,1-2,4,8-10H2,3,5-6H3/t13-,14+,15-/m1/s1
FormulaC15H24
PubChem ID6918391
Molweight204.35
LogP6.1
Atoms15
Bonds3
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID62854
Supernatural-IDSN0271562-04

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaFusarium OxysporumNAWeikl et al. 2016
EukaryotaFusarium CulmorumNASchmidt et al. 2018
EukaryotaAspergillus KawachiiNADickschat et al. 2018
ProkaryotaStreptomyces Philanthiantifungal activity against Aspergillus parasiticus TISTR 3276 and Aspergillus flavus PSRDC-4NABoukaew and Prasertsan 2020
EukaryotaPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al. 2000
EukaryotaLaccaria BicolornanaDitengou et al. 2015
EukaryotaHypoxylon Anthochroumnaendophytic in Bursera lancifoliaUlloa-Benítez et al. 2016
EukaryotaTrichoderma VirensNACrutcher et al. 2013
EukaryotaTrichoderma AtrovirideNACrutcher et al. 2013
EukaryotaTrichoderma ReeseiNACrutcher et al. 2013
EukaryotaAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
ProkaryotaStreptomyces Citreusn/aNASchulz and Dickschat 2007
EukaryotaPenicillium Roquefortin/aobtained fronm department of Biotechnology , Denmark Technical Universität at CopenhagenJelen 2003
EukaryotaPholiota Squarrosan/aNAMueller et al. 2013
EukaryotaLaccaria Bicolorn/aNAMueller et al. 2013
EukaryotaPaxillus Involutusn/aNAMueller et al. 2013
EukaryotaArmillaria Mellean/aNAMueller et al. 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaFusarium OxysporumSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaFusarium CulmorumKing`s B agarUPLC-MSno
EukaryotaAspergillus Kawachiimedium 129CLSA-GCMSno
ProkaryotaStreptomyces Philanthisterile wheat seedsGC-MSno
EukaryotaPiptoporus BetulinusnaGC/MSno
EukaryotaLaccaria Bicolormodified Pachlewski mediumcapillary gas chromatography, GC/MSyes
EukaryotaHypoxylon AnthochroumPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSno
EukaryotaTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
EukaryotaTrichoderma ReeseiPotato dextrose agarHS-SPME/GC-MS no
EukaryotaAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
ProkaryotaStreptomyces Citreusn/an/ano
EukaryotaPenicillium Roqueforti wheat kernel mediumincubated at 20°C for 14 days, isolation by SPME with different fibresno
EukaryotaPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MSno
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


(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane

Compound Details

Synonymous names
beta-Cedrene
(+)-beta-Cedrene
546-28-1
.beta.-Cedrene
(+)-.beta.-Cedrene
6QL7ERD5Q1
1H-3a,7-Methanoazulene, octahydro-3,8,8-trimethyl-6-methylene-, (3R,3aS,7S,8aS)-
(+)-beta-Funebrene
Cedr-8(15)-ene
(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane
(3R,3aS,7S,8aS)-3,8,8-Trimethyl-6-methyleneoctahydro-1H-3a,7-methanoazulene
1H-3a,7-Methanoazulene, octahydro-3,8,8-trimethyl-6-methylene-, [3R-(3.alpha.,3a.beta.,7.beta.,8a.alpha.)]-
1H-3A,7-METHANOAZULENE, OCTAHYDRO-3,8,8-TRIMETHYL-6-METHYLENE-, (3R-(3.ALPHA.,3A.BETA.,7.BETA.,8A.ALPHA.))-
EINECS 208-898-8
(+)-ss-Cedrene
(+)- beta -Cedrene
UNII-6QL7ERD5Q1
DTXSID40883435
HY-N11706
AKOS015896901
FS-7321
1H-3a,7-Methanoazulene,octahydro-3,8,8-trimethyl-6-methylene-,(3R,3aS,7S,8aS)-
1H-3a,7-Methanoazulene, octahydro-3,8,8-trimethyl-6-methylene-, (3R-(3alpha,3abeta,7beta,8aalpha))-
CS-0783420
(+)-beta-Cedrene (major, contains (-)-cedrene)
(+)-beta-Cedrene, >=95.0% (sum of enantiomers, GC)
(3R-(3alpha,3Abeta,7beta,8aalpha))-octahydro-3,8,8-trimethyl-6-methylene-1H-3a,7-methanoazulene
Microorganism:

Yes

IUPAC name(1S,2R,5S,7S)-2,6,6-trimethyl-8-methylidenetricyclo[5.3.1.01,5]undecane
SMILESCC1CCC2C13CCC(=C)C(C3)C2(C)C
InchiInChI=1S/C15H24/c1-10-7-8-15-9-12(10)14(3,4)13(15)6-5-11(15)2/h11-13H,1,5-9H2,2-4H3/t11-,12+,13+,15+/m1/s1
FormulaC15H24
PubChem ID11106485
Molweight204.35
LogP4.9
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAlternaria AlternataNAWeikl et al. 2016
EukaryotaFusarium OxysporumNAWeikl et al. 2016
EukaryotaFusarium Oxysporum0NALi et al. 2018
EukaryotaFusarium OxysporumNALi et al. 2018
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
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Kluyveromyces MarxianusJi et al. 2024
Saccharomyces CerevisiaeJi et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAlternaria AlternataSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaFusarium OxysporumSynthetic nutrientHead-space sorptive extraction, GC-MSno
EukaryotaFusarium OxysporumPDA plateSPME-GC-MSno
EukaryotaFusarium Oxysporumpotato dextrose agarSPME, GC-MSno
EukaryotaMrakia Blollopisartificial nectar mediaGC-MSno
EukaryotaTausonia Pullulansartificial nectar mediaGC-MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
Kluyveromyces MarxianusSauce Meat during StorageSPME–GC–MSno
Saccharomyces CerevisiaeSauce Meat during StorageSPME–GC–MSno


(1R,8S)-2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-ene

Compound Details

Synonymous names
Isolongifolene
(-)-Isolongifolene
1135-66-6
iso-Longifolene
(+/-)-Isolongifolene
Isolongifolene, (-)-
Isolongifolene, (+/-)-
PX6N25M90H
E0LN4V7EY4
UNII-PX6N25M90H
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-
DTXSID1044518
17015-38-2
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (+/-)-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S,4aR)-
2H-2,4a-Methanonaphthalene,1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S,4aR)-
2H-2alpha,4aalpha-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (+/-)-
UNII-E0LN4V7EY4
EINECS 214-494-2
(1R)-2,2,7,7-Tetramethyltricyclo[6.2.1.01.6]undec-5-ene
(1R,8S)-2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-ene
CHEMBL3183415
DTXCID9024518
CQUAYTJDLQBXCQ-NHYWBVRUSA-N
HY-N7363
Tox21_302253
MFCD00042616
(-)-Isolongifolene(-)-Isolongifolene
(2S)-1,3,4,5,6,7-Hexahydro-1,1,5,5-tetramethyl-2H-2,4a-methanonaphthalene
NCGC00255851-01
CAS-1135-66-6
CS-0113874
NS00012552
J-002993
Q63392412
(-)-Isolongifolene, >=98.0% (sum of enantiomers, GC)
(1R,8S)-2,2,7,7-TETRAMETHYLTRICYCLO[6.2.1.0(1),?]UNDEC-5-ENE
2H-2.ALPHA.,4A.ALPHA.-METHANONAPHTHALENE, 1,3,4,5,6,7-HEXAHYDRO-1,1,5,5-TETRAMETHYL-, (+/-)-
Microorganism:

No

IUPAC name(1R,8S)-2,2,7,7-tetramethyltricyclo[6.2.1.01,6]undec-5-ene
SMILESCC1(CCC=C2C13CCC(C3)C2(C)C)C
InchiInChI=1S/C15H24/c1-13(2)8-5-6-12-14(3,4)11-7-9-15(12,13)10-11/h6,11H,5,7-10H2,1-4H3/t11-,15-/m0/s1
FormulaC15H24
PubChem ID11127402
Molweight204.35
LogP5
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
Supernatural-IDSN0053116-02

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


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

Compound Details

Synonymous names
(+)-thujopsene
cis-Thujopsene
470-40-6
(1aR,4aR,8aR)-2,4a,8,8-tetramethyl-1,1a,4,4a,5,6,7,8-octahydrocyclopropa[d]naphthalene
CHEBI:61737
DTXSID50881245
Cyclopropa(D)Naphthalene, 1,1A,4,4A,5,6,7,8-Octahydro-2,4A,8,8-Tetramethyl-, (1As,4As,8As)
C20724
Q27131354
(1S,6S,10S)-2,2,6,9-Tetramethyltricyclo[8.1.0.01.6]undec-8-ene
(1aR,4aR,81R)-2,4a,8,8-tetramethyl-1,1a,4,4a,5,6,7,8-octahydrocyclopropa[d]naphthalene
Microorganism:

No

IUPAC name(1aR,4aR,8aR)-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-/m1/s1
FormulaC15H24
PubChem ID11401461
Molweight204.35
LogP4.8
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID61737
Supernatural-IDSN0422771-02

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPenicillium Decumbensmalt 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


3-methylidene-6-(1,2,2-trimethylcyclopentyl)cyclohexene

Compound Details

Synonymous names
delta-cuprenene
.delta.-Cuprenene
QPXHUMFBJLASJO-UHFFFAOYSA-N
(R)-3-Methylene-6-((S)-1,2,2-trimethylcyclopentyl)cyclohex-1-ene
Cyclohexene, 3-methylene-6-(1,2,2-trimethylcyclopentyl)-, [S-(R*,S*)]-
Microorganism:

No

IUPAC name3-methylidene-6-(1,2,2-trimethylcyclopentyl)cyclohexene
SMILESCC1(CCCC1(C)C2CCC(=C)C=C2)C
InchiInChI=1S/C15H24/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(15,2)3/h6,8,13H,1,5,7,9-11H2,2-4H3
FormulaC15H24
PubChem ID25202927
Molweight204.35
LogP5.4
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
Supernatural-IDSN0312001

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus FischeriNADickschat et al. 2018
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus Fischerimedium 129CLSA-GCMSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno


(1S,6S,7S,8S)-1-methyl-3-methylidene-8-propan-2-yltricyclo[4.4.0.02,7]decane

Compound Details

Synonymous names
beta-Copaene
(1S,6S,7S,8S)-1-methyl-3-methylene-8-(propan-2-yl)-tricyclo[4.4.0.0(2,7)]decane
(1S,6S,7S,8S)-8-isopropyl-1-methyl-3-methylenetricyclo[4.4.0.0(2,7)]decane
CHEBI:64799
C20274
Q27133439
Microorganism:

Yes

IUPAC name(1S,6S,7S,8S)-1-methyl-3-methylidene-8-propan-2-yltricyclo[4.4.0.02,7]decane
SMILESCC(C)C1CCC2(C3C1C2C(=C)CC3)C
InchiInChI=1S/C15H24/c1-9(2)11-7-8-15(4)12-6-5-10(3)14(15)13(11)12/h9,11-14H,3,5-8H2,1-2,4H3/t11-,12-,13-,14?,15-/m0/s1
FormulaC15H24
PubChem ID57339298
Molweight204.35
LogP4.7
Atoms15
Bonds1
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes
CHEBI-ID64799
Supernatural-IDSN0376929-06

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaFusarium CulmorumNASchmidt et al. 2018
EukaryotaAspergillus KawachiiNADickschat et al. 2018
ProkaryotaStreptomyces GriseusNARiu et al. 2022
EukaryotaFomitopsis PinicolanaGermanyRösecke et al. 2000
EukaryotaAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
ProkaryotaChondromyces Crocatusn/aNASchulz et al. 2004
ProkaryotaStigmatella Aurantiacan/aNADickschat et al. 2005_5
ProkaryotaStigmatella Aurantiacan/aNASchulz and Dickschat 2007
Fusarium GraminearumBallot et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaFusarium CulmorumKing`s B agarUPLC-MSno
EukaryotaAspergillus Kawachiimedium 129CLSA-GCMSno
ProkaryotaStreptomyces GriseusTSA mediaSPME/GC-MSno
EukaryotaFomitopsis PinicolanaGC/MSno
EukaryotaAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
ProkaryotaChondromyces Crocatusn/an/ano
ProkaryotaStigmatella Aurantiacan/an/ano
Fusarium Graminearumtryptone soy (TS medium; Carl Roth, Karlsruhe, Germany)GC-QQQ-MSno


(1R,2S,5S,7R)-2,6,6,8-tetramethyltricyclo[5.3.1.01,5]undec-8-ene

Compound Details

Synonymous names
2-epi-.alpha.-Funebrene
IRAQOCYXUMOFCW-SFDCQRBFSA-N
Microorganism:

No

IUPAC name(1R,2S,5S,7R)-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+/m0/s1
FormulaC15H24
PubChem ID91753249
Molweight204.35
LogP4.6
Atoms15
Bonds0
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al. 2012
EukaryotaPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al. 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno
EukaryotaPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSno