Results for:
Species: Laccaria bicolor S238N

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

Compound Details

Synonymous names
delta-Amorphene
DELTA-CADINENE
AC1L9ADP
C6H8P2
6614AB
X3450
CHEMBL445759
7848KI47OS
C06394
AK110299
ZINC8220462
UNII-7848KI47OS
CHEBI:15385
DTXSID70858792
AJ-57371
(+)-delta-Cadinene
AKOS016008860
(1S,8aR)-delta-cadinene
(+)-D-Cadinene
LMPR0103330001
483-76-1
Cadina-1(10),4-diene
(1S,8aR)-1-Isopropyl-4,7-dimethyl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-1-isopropyl-4,7-di-methyl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthalene
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
Molweight204.357
LogP4.4
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolorn/aMueller et al., 2013
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiTrichoderma Viriden/aMueller et al., 2013
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
BacteriaStreptomyces Caviscabiesn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Citreusn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
FungiAspergillus UstusPolizzi et al., 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPiptoporus BetulinusnaGC/MSNo
BacteriaStreptomyces Caviscabiesn/an/a
BacteriaStreptomyces Citreusn/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS


1,6-dimethyl-4-propan-2-yl-1,2,3,7,8,8a-hexahydronaphthalene

Mass-Spectra

Compound Details

Synonymous names
Epizonarene
FIAKMTRUEKZMNO-UHFFFAOYSA-N
AC1LC6UO
4,6-Cadinadiene
CTK8I6853
4-Isopropyl-1,6-dimethyl-1,2,3,7,8,8a-hexahydronaphthalene
4-Isopropyl-1,6-dimethyl-1,2,3,7,8,8a-hexahydronaphthalene #
1,6-dimethyl-4-propan-2-yl-1,2,3,7,8,8a-hexahydronaphthalene
IUPAC name1,6-dimethyl-4-propan-2-yl-1,2,3,7,8,8a-hexahydronaphthalene
SMILESCC1CCC(=C2C1CCC(=C2)C)C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,12,14H,5-8H2,1-4H3
FormulaC15H24
PubChem ID595385
Molweight204.357
LogP4.4
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPholiota Squarrosan/aMueller et al., 2013
FungiVerticillium Longisporumn/aMueller et al., 2013
BacteriaChondromyces Crocatusn/aSchulz and Dickschat, 2007
BacteriaChondromyces Crocatus Cm C2n/aSchulz et al., 2004
BacteriaChondromyces Crocatus Cm C5n/aSchulz et al., 2004
BacteriaStreptomyces Caviscabiesn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiVerticillium LongisporumMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
BacteriaChondromyces Crocatusn/an/a
BacteriaChondromyces Crocatus Cm C2n/an/a
BacteriaChondromyces Crocatus Cm C5n/an/a
BacteriaStreptomyces Caviscabiesn/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a


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

Compound Details

Synonymous names
OPFTUNCRGUEPRZ-QLFBSQMISA-N
AC1OCFDE
beta-Elemen
BETA-ELEMENE
Levo-beta-elemene
2QG8CX6LXD
UNII-2QG8CX6LXD
8064AH
SDP-111
CHEMBL448502
C17094
CHEBI:62855
ZINC14096289
E- .beta.-Elemene
2,4-Diisopropenyl-1-methyl-1-vinylcyclohexane
(-)-beta-Elemene
Epitope ID:153551
AKOS028108977
(-)-beta-Elemene, analytical standard
515-13-9
beta-Elemene, (-)-
33880-83-0
20296-36-0
11033-44-6
154028-29-2
1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-cyclohexane
(1S,2S,4R)-2,4-diisopropenyl-1-methyl-1-vinylcyclohexane
(1S,2S,4R)-(-)-1-methyl-1-vinyl-2,4-diisopropenylcyclohexane
Cyclohexane, 2,4-diisopropenyl-1-methyl-1-vinyl-, (1S,2S,4R)-
(1S,2S,4R)-1-ethenyl-1-methyl-2,4-bis(prop-1-en-2-yl)cyclohexane
(1S,2S,4R)-1-ethenyl-1-methyl-2,4-di(prop-1-en-2-yl)cyclohexane
(1S,2S,4R)-1-methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S,2S,4R)-
Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S-(1-alpha,2-beta,4-beta))-
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
Molweight204.357
LogP4.74
Atoms39
Bonds39
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiHypoxylon Antochroum Blacinaendophytic in Bursera lancifoliaUlloa-Benítez et al., 2016
FungiTrichoderma AtrovirideCrutcher et al., 2013
FungiTrichoderma ReeseiCrutcher et al., 2013
FungiTrichoderma VirensCrutcher et al., 2013
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolorn/aMueller et al., 2013
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al., 2012
BacteriaStreptomyces Citreusn/aSchulz and Dickschat, 2007
FungiAspergillus UstusPolizzi et al., 2012
FungiPericonia BritannicaPolizzi et al., 2012
FungiPenicillium Roqueforti (IBT 16404)n/aobtained fronm department of Biotechnology , Denmark Technical Universität at CopenhagenJelen, 2003
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2019
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiHypoxylon Antochroum BlaciPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSNo
FungiTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
FungiTrichoderma ReeseiPotato dextrose agarHS-SPME/GC-MS no
FungiTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPiptoporus BetulinusnaGC/MSNo
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
BacteriaStreptomyces Citreusn/an/a
FungiAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiPericonia Britannicamalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiPenicillium Roqueforti (IBT 16404) wheat kernel mediumincubated at 20°C for 14 days, isolation by SPME with different fibres
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)malt extract agarSBSE-GC-MSno


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

Compound Details

Synonymous names
Muurolene
alpha-Muurolene
B1-Cadinene
C20272
CHEBI:64797
(+)-alpha-muurolene
DTXSID90144629
10208-80-7
(1S,4aS,8aR)-1-isopropyl-4,7-dimethyl-1,2,4a,5,6,8a-hexahydronaphthalene
(1S,4aS,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,4a,5,6,8a-hexahydronaphthalene
Naphthalene, 1,2,4a,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S-(1alpha,4aalpha,8aalpha))-
IUPAC name(1S,4aS,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene
SMILESCC1=CC2C(CC1)C(=CCC2C(C)C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h6,9-10,13-15H,5,7-8H2,1-4H3/t13-,14+,15-/m0/s1
FormulaC15H24
PubChem ID12306047
Molweight204.357
LogP4.45
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiAspergillus Vesicolorcompost Fischer et al. 2041
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPenicillium Glabrumcompost Fischer et al. 2041
BacteriaChondromyces Crocatusn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Caviscabiesn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
FungiAspergillus UstusPolizzi et al., 2012
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiSpongiporus Leucomallellusnasaprophytic mostly on wet, old pinesZiegenbein et al., 2006
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiAspergillus Vesicoloryest extract sucroseTenax/GC-MSno
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPenicillium Glabrumyest extract sucroseTenax/GC-MSno
BacteriaChondromyces Crocatusn/an/a
BacteriaStreptomyces Caviscabiesn/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiFomitopsis PinicolanaGC/MSNo
FungiSpongiporus LeucomallellusnaGC/MSNo


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

Mass-Spectra

Compound Details

Synonymous names
RMZHSBMIZBMVMN-UHFFFAOYSA-N
gamma-Selinene
AC1LAVGE
4a-methyl-1-methylidene-7-(propan-2-ylidene)-decahydronaphthalene
4(15),7(11)-Eudesmadiene
(4aR,8aS)-4a-Methyl-1-methylene-7-(propan-2-ylidene)decahydronaphthalene
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethylidene)-, trans-
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethylidene)-, (4aR,8aS)-
8a-methyl-4-methylidene-6-propan-2-ylidene-2,3,4a,5,7,8-hexahydro-1H-naphthalene
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
Molweight204.357
LogP4.48
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPleurotus Eryngii Var. TuoliensisnanaUsami et al., 2014
FungiTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPleurotus Eryngii Var. TuoliensisnaGC/MS, GC-O, AEDANo
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene

Compound Details

Synonymous names
Caryophyllene
trans-Caryophyllene
NPNUFJAVOOONJE-GFUGXAQUSA-N
BETA-CARYOPHYLLENE
Beta-Caryophylene
trans-beta-caryophyllene
L-Caryophyllene
Caryophyllene B
AC1NQYK7
.beta.-Caryophyllen
.beta.-Caryophyllene
trans-.beta.-Caryophyllene
BHW853AU9H
(E)-Caryophyllene
.beta.-trans-Caryophyllene
AC1Q2A41
C15H24
UNII-BHW853AU9H
(E)-beta-caryophyllene
E-.beta.-caryophyllene
V0915
(E)-beta-caryophylene
NSC11906
CHEMBL445740
Caryophyllene, (E)
(-)-Caryophyllene
C09629
OR355343
(-)-trans-Caryophyllene
ST072181
DTXSID8024739
DR000334
DSSTox_CID_4739
CHEBI:10357
ZINC8234282
(-)-beta-caryophyllene
DSSTox_GSID_24739
(-)-trans-Caryophyllene, analytical standard
ZINC08234282
MFCD00075925
DSSTox_RID_77517
.beta.-(E)-Caryophyllene
W-109317
AKOS024283988
FT-0603049
LMPR0103120001
87-44-5
Tox21_301497
beta-Caryophyllene, >=80%, FCC, FG
(-)-(E)-Caryophyllene
CAS-87-44-5
NCGC00142620-01
NCGC00255159-01
.beta.-Caryophyllene, (-)
MolPort-001-793-250
(-)-trans-Caryophyllene, >=98.5% (sum of enantiomers, GC)
(1S,9R)-6,10,10-trimethyl-2-methylenebicyclo[7.2.0]undec-5-ene
trans-(1R,9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene
trans-(1R,9S)-8-Methylene-4,11,11-trimethylbicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene
(1R,4E,9S)-4,11,11-trimethyl-8-methylene-bicyclo[7.2.0]undec-4-ene
8-Methylene-4,11,11-(trimethyl)bicyclo(7.2.0)undec-4-ene, (1R,4E,9S)-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (E)-(1R,9S)-(-)-
Bicyclo[7.2.0]undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-
Bicyclo(7.2.0)undec-4-ene, 8-methylene-4,11,11-trimethyl-, (E)-(1R,9S)-(-)-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R-(1R*,4E,9S*)]-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R- (1R*,4E,9S*)]-
IUPAC name(1R,4E,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
SMILESCC1=CCCC(=C)C2CC(C2CC1)(C)C
InchiInChI=1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6+/t13-,14-/m1/s1
FormulaC15H24
PubChem ID5281515
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiPenicillium Clavigerumcompost Fischer et al. 2027
FungiCU Fusarium Oxysporum Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiFusarium Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPhialophora Fastigiata ConantnanaSunesson et al., 1995
FungiTrichodema Viriden/aWheatley et al., 1997
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPhoma Sp.n/aStrobel et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiPenicillium Clavigerumyest extract sucroseTenax/GC-MSno
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPhialophora Fastigiata ConantDG18GC/MS
FungiTrichodema VirideMalt extractGC/MS
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSyes
FungiFomitopsis PinicolanaGC/MSNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPhoma Sp.n/aSolid phase microextraction (SPME)


(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
YOVSPTNQHMDJAG-QLFBSQMISA-N
BETA-SELINENE
beta-Eudesmene
AC1L9CQH
.beta.-Selinene
.beta.-Eudesmene
C09723
OR115896
CHEMBL2287242
ZINC8234293
CHEBI:10443
(+)-beta-Selinene
LMPR0103190014
(+)-.beta.-Selinene
17066-67-0
Eudesma-4(14),11-diene
Selina-4(14),11-diene
(4aR,7R,8aS)-7-isopropenyl-4a-methyl-1-methylenedecahydronaphthalene
[4aR-(4aalpha,7alpha,8abeta)]-decahydro-4a-methyl-1-methylene-7-(1-methylethenyl)-naphthalene
(4aR,7R,8aS)-4a-methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalene
7-Isopropenyl-4a-methyl-1-methylenedecahydronaphthalene-, (4aR-(4a.alpha.,7.alpha.,8a.beta.))-
(4aR,7R,8aS)-4a-methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalene eudesma-4(14),11-diene
Naphthalene, decahydro-4a-methyl-1-methylene-7-(1-methylethenyl)-, [4aR-(4a.alpha.,7.alpha.,8a.beta.)]-
(3R,4aS,8aR)-8a-methyl-5-methylidene-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene
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
Molweight204.357
LogP4.58
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPericonia Britannicanawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPericonia BritannicaPolizzi et al., 2012
FungiPhoma Sp.n/aStrobel et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPericonia Britannicamalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPericonia Britannicamalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiPhoma Sp.n/aSolid phase microextraction (SPME)


Compound Details

Synonymous names
alpha-Ylangene
AC1L9CRH
C09749
PL020546
CHEBI:10341
14912-44-8
(1S)-1,3-DIMETHYL-8-(PROPAN-2-YL)TRICYCLO[4.4.0.0(2),?]DEC-3-ENE
IUPAC name
SMILESCC1=CCC2C3C1C2(CCC3C(C)C)C
InchiInChI=1S/C15H24/c1-9(2)11-7-8-15(4)12-6-5-10(3)14(15)13(11)12/h5,9,11-14H,6-8H2,1-4H3/t11?,12?,13?,14?,15-/m0/s1
FormulaC15H24
PubChem ID442409
Molweight204.357
LogP4.09
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiTrichoderma Viriden/aMueller et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace ( using stir bar sorptive extraction )/ GC-MS


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

Compound Details

Synonymous names
QMAYBMKBYCGXDH-SOUVJXGZSA-N
.alpha.-Cadinene
(?)-alpha-Amorphene
(+)-alpha-amorphene
(-)-.alpha.-Cadinene
23515-88-0
.alpha.-Cadinene, (-)-
Cadina-4,9-diene-, (-)-
(1S,4aR,8aR)-1-Isopropyl-4,7-dimethyl-1,2,4a,5,6,8a-hexahydronaphthalene
[1s-(1a,4ab,8aa)]-1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1methylethyl)-naphthalene
Naphthalene, 1,2,4a,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, (1S,4aR,8aR)-
Naphthalene, 1,2,4a,5,6,8a-hexahydro-4,7-dimethyl-1-(1-methylethyl)-, [1S-(1.alpha.,4a.beta.,8a.alpha.)]-
IUPAC name(1S,4aR,8aS)-4,7-dimethyl-1-propan-2-yl-1,2,4a,5,6,8a-hexahydronaphthalene
SMILESCC1=CC2C(CC1)C(=CCC2C(C)C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h6,9-10,13-15H,5,7-8H2,1-4H3/t13-,14-,15+/m0/s1
FormulaC15H24
PubChem ID12306052
Molweight204.357
LogP4.45
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolorn/aMueller et al., 2013
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiTrichoderma Viriden/aMueller et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS


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

Compound Details

Synonymous names
JUQGWBAOQUBVFP-OPFPJEHXSA-N
AC1O537I
Cadina-1,4-diene
Cadina-1,4-diene, cis
Cadina-1(2),4-diene
(1S,4S,4aR)-4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7-hexahydronaphthalene
(1S)-1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7-hexahydronaphthalene-, [1S-(1.alpha.,4.alpha.,4a.alpha.)]-
Naphthalene, 1,2,3,4,4a,7-hexahydro-1,6-dimethyl-4-(1-methylethyl)-, [1S-(1.alpha.,4.alpha.,4a.alpha.)]-
IUPAC name(1S)-1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene
SMILESCC1CCC(C2C1=CCC(=C2)C)C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h7,9-10,12-13,15H,5-6,8H2,1-4H3/t12-,13?,15?/m0/s1
FormulaC15H24
PubChem ID6427091
Molweight204.357
LogP4.45
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPholiota Squarrosan/aMueller et al., 2013
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiTrichoderma Viriden/aMueller et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS


(1aR,4R,7R,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,5,6,7,7b-octahydrocyclopropa[e]azulene

Compound Details

Synonymous names
(-)-Isoledene
DTXSID40572716
ZINC57989145
FT-0642315
95910-36-4
(-)-Isoledene, >=95.0% (sum of enantiomers, GC)
(1aR,4R,7R,7bS)-1,1,4,7-Tetramethyl-1a,2,3,4,5,6,7,7b-octahydro-1H-cyclopropa[e]azulene
IUPAC name(1aR,4R,7R,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,5,6,7,7b-octahydrocyclopropa[e]azulene
SMILESCC1CCC2C(C2(C)C)C3=C1CCC3C
InchiInChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h9-10,12,14H,5-8H2,1-4H3/t9-,10-,12-,14-/m1/s1
FormulaC15H24
PubChem ID15431199
Molweight204.357
LogP4.04
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiFusarium Culmorum PVnasandy dune soil, NetherlandsSchmidt et al., 2016
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiFusarium Culmorum PVwater agar supplied with artificial root exudatesGC/MS-Q-TOFNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes


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

Compound Details

Synonymous names
Sesquichamene
Thujopsene
WIDDRENE
cis-Thujopsene
AC1L9CR2
CTK8F1421
VC30563
E116U47P7N
CHEBI:9578
C09740
(-)-Thujopsene
PL001566
ZINC8234295
A827133
(-)-Thujopsen
UNII-E116U47P7N
(-)-widdrene
CC-00064
NSC 44707
C-10040
AKOS015914102
I14-45277
LMPR0103860001
Thujopsene, (-)-
470-40-6
EINECS 207-426-8
(-)-Thujopsene, >=97.0% (GC)
(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,5,6,7-hexahydrocyclopropa[j]naphthalene
(1S,6S,10S)-2,2,6,9-Tetramethyltricyclo[8.1.0.01.6]undec-8-ene
(1aS,4aS,8aS)-2,4a,8,8-tetramethyl-1,1a,4,4a,5,6,7,8-octahydrocyclopropa[d]naphthalene
(4AS,8AS,8BS)-2,4A,8,8-TETRAMETHYL-1H,4H,4AH,5H,6H,7H,8H,8BH-CYCLOPROPA[E]NAPHTHALENE
(1AS-(1aalpha,4abeta,8aR*))-1,1a,4,4a,5,6,7,8-octahydro-2,4a,8,8-tetramethylcyclopropa(d)naphthalene
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,4aS,8aS)-
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
Molweight204.357
LogP4.11
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238Nstimulates lateral root (LR) formation in Arabidopsis thaliana and Populus sp.naDitengou et al., 2015
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2023
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2040
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)malt extract agarSBSE-GC-MSno
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)malt extract agarSBSE-GC-MSno


4,4-dimethylpentan-2-one

Mass-Spectra

Compound Details

Synonymous names
AZASWMGVGQEVCS-UHFFFAOYSA-N
Neopentyl methyl ketone
Methyl neopentyl ketone
Methyl neoamyl ketone
ACMC-1AWGM
AC1L1XL1
NSC944
AC1Q1K42
OR0844
CTK5A9363
neo-C5H11COCH3
NSC-944
SCHEMBL104505
VZ27540
OR099241
OR000375
DTXSID4073914
ZINC1587723
A832134
CJ-25357
KB-35494
4,4-DIMETHYLPENTAN-2-ONE
ZINC01587723
MFCD00008854
4,4-Dimethyl-2-pentanone
2,2-dimethyl-4-pentanone
DB-053310
TC-169212
AKOS009156830
4,4-DIMETHYL-2-PENTA
FT-0632456
I14-50276
4,4-dimethyl-pentan-2-one
2-Pentanone,4,4-dimethyl-
590-50-1
Z2235409406
2-Pentanone, 4,4-dimethyl-
EINECS 209-685-2
4,4-Dimethyl-2-pentanone, 99%
MolPort-001-757-203
InChI=1/C7H14O/c1-6(8)5-7(2,3)4/h5H2,1-4H
IUPAC name4,4-dimethylpentan-2-one
SMILESCC(=O)CC(C)(C)C
InchiInChI=1S/C7H14O/c1-6(8)5-7(2,3)4/h5H2,1-4H3
FormulaC7H14O
PubChem ID11546
Molweight114.188
LogP1.84
Atoms22
Bonds21
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationKetones

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes


4,7,7-trimethylbicyclo[4.1.0]hept-3-ene

Mass-Spectra

Compound Details

Synonymous names
Monoterpenes
BQOFWKZOCNGFEC-UHFFFAOYSA-N
Carene
alpha-Carene
AC1L1AAR
d3-carene
3-Carene
Delta-3-Carene
ACMC-1ADO8
3-Carene, analytical standard
AC1Q29W8
S-3-Carene
CTK3J2995
NE10089
Delta(3)-Carene
CHEMBL506854
Delta-car-3-ene
OR126426
OR038357
DTXSID4047462
OR126427
delta(sup 3)-Carene
SBB060476
CHEBI:35661
3-Karen [Czech]
AN-18424
ANW-19700
.delta. 3-carene
FCH1117427
LS-43716
LS-52533
DSSTox_GSID_47462
3-.delta.-Carene
DSSTox_RID_82362
DSSTox_CID_27462
3-Carene, >=90%
3-Carene, 90%
ST51046655
TR-004700
DB-063033
RTR-004700
AKOS015840953
Delta 3 Carene 90 PF
W-110341
FT-0624500
.DELTA.-caR-3-ene
BRN 1902766
I14-52597
Tox21_302632
(+)Car-3-ene
4,7,7-Trimethyl-3-norcarene
(+-)-delta3-Carene
EN300-173315
NCGC00256842-01
MCULE-2811504753
(+-)-3-Carene
EINECS 236-719-3
13466-78-9
74806-04-5
CAS-13466-78-9
MolPort-006-120-436
3-Norcarene, 3,7,7-trimethyl-
3,7,7-Trimethylbicyclo[4.1.0]-3-heptene
3,7,7-Trimethylbicyclo(4.1.0)hept-3-ene
3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
4,7,7-trimethylbicyclo[4.1.0]hept-3-ene
3,7,7-trimethyl-bicyclo[4.1.0]hept-3-ene
Bicyclo(4.1.0)hept-3-ene, 3,7,7-trimethyl-
Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-
3,7,7(or 4,7,7)-Trimethylbicyclo(4.1.0)hept-3-ene
Bicyclo[4.1.0]hept-3-ene, 3,7,7-trimethyl-, (1S)-
Bicyclo(4.1.0)hept-3-ene, 3,7,7(or 4,7,7)-trimethyl-
Bicyclo[4.1.0]hept-3-ene, 3,7,7(or 4,7,7)-trimethyl-
IUPAC name4,7,7-trimethylbicyclo[4.1.0]hept-3-ene
SMILESCC1=CCC2C(C1)C2(C)C
InchiInChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3
FormulaC10H16
PubChem ID26049
Molweight136.238
LogP2.8
Atoms26
Bonds27
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaBacillus Pumilus ES4promotion of performance of Chlorella sorokiniana ShihAmavizca et al. 2017
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiCenococcum GeophilumnanaDitengou et al., 2015
FungiFusarium Culmorum PVaffects swarming and swimming motility of Serratia plymuthica PRI-2C; affects swarming ability of Collimonas pratensis Ter291sandy dune soil, NetherlandsSchmidt et al., 2016
FungiFusarium Graminearum 15AcDONn/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON 1001tan/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON ZFR 29n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_4n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_5n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_6n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_7n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_8n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_9n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1002tn/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 11791n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1509n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 8046n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL38369n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL6394n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 15n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 37n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 51n/aBusko et al., 2014
FungiFusarium Graminearum NIVn/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 119n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 23n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 48n/aBusko et al., 2014
FungiFusarium Graminearum NIV_5n/aBusko et al., 2014
FungiFusarium Graminearum NIV_6n/aBusko et al., 2014
FungiFusarium Graminearum NIV_7n/aBusko et al., 2014
FungiFusarium Graminearum NIV_8n/aBusko et al., 2014
FungiFusarium Graminearum NIV_9n/aBusko et al., 2014
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiOgataea Pininamycangia of Dendroctonus brevicomisDavis et al., 2011
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
BacteriaPropionibacterium Acidifaciens DSM 21887 as a biomarker for a breath test for detection of cariesHertel et al., 2015
BacteriaStreptococcus Mutans DSM 20523 as a biomarker for a breath test for detection of cariesHertel et al., 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaBacillus Pumilus ES4TSASPME-GCno
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiCenococcum Geophilummodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiFusarium Culmorum PVwater agar supplied with artificial root exudatesGC/MS-Q-TOFNo
FungiFusarium Graminearum 15AcDONyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON 1001tayeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON ZFR 29yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_4yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_9yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1002tyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 11791yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1509yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 8046yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL38369yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL6394yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 15yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 37yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 51yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIVyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 119yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 23yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 48yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_9yeast extract sucrose agarSPME/GC-MS
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiOgataea PiniMEAGC/MS
FungiPiptoporus BetulinusnaGC/MSNo
BacteriaPropionibacterium Acidifaciens DSM 21887Brain-Heart-Infusion agarTenaxâ„¢-trap/GC-MS
BacteriaStreptococcus Mutans DSM 20523Brain-Heart-Infusion agarTenaxâ„¢-trap/GC-MS


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

Compound Details

Synonymous names
WRHGORWNJGOVQY-RBSFLKMASA-N
GAMMA-CADINENE
AC1L3NV1
AC1Q29YU
2GHT32E0JU
UNII-2GHT32E0JU
(?)-gamma-Cadinene
C19738
trans- .gamma.-Cadinene
OR265993
CHEBI:63203
(-)-gamma-cadinene
(-)-g-cadinene
gamma-Cadinene, (-)-
1460-97-5
39029-41-9
(1R,4aS,8aS)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
(1R,4aS,8aS)-7-methyl-4-methylidene-1-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
C15 H24, NAPHTHALENE, 1,2,3,4,4A,5,6,8A-OCTAHYDRO-7-METHYL-4-METHYLENE-1-(1-METHYLETHYL)-
Naphthalene, 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4-methylene-1-(1-methylethyl)-, (1alpha,4abeta,8aalpha)-
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
Molweight204.357
LogP4.51
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiAspergillus UstusPolizzi et al., 2012
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2033
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2046
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)malt extract agarSBSE-GC-MSno
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)malt extract agarSBSE-GC-MSno
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiFomitopsis PinicolanaGC/MSNo