Results for:
Species: Alternaria alternata(Fr.)Keissler (DSMZ 62010)

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

Compound Details

Synonymous names
AC1NSV6N
(3R,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene
IUPAC name(3R,5S)-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?/m0/s1
FormulaC15H24
PubChem ID5317160
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaChondromyces Crocatusn/aSchulz et al., 2004
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2031
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2044
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaChondromyces Crocatusn/an/a
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


(7S,9aS)-4,4,7,9a-tetramethyl-1,2,3,6,8,9-hexahydrobenzo[7]annulen-7-ol

Compound Details

Synonymous names
Widdrol
AC1L3S0E
AC1Q59NR
CHEMBL2253133
OR328218
SCHEMBL6519819
6892-80-4
(7S,9aS)-4,4,7,9a-tetramethyl-1,2,3,6,8,9-hexahydrobenzo[7]annulen-7-ol
1H-Benzocyclohepten-7-ol, 2,3,4,4a,5,6,7,8-octahydro-1,1,4a,7-tetramethyl-, cis-
1H-Benzocyclohepten-7-ol, 2,3,4,4a,5,6,7,8-octahydro-1,1,4a,7-tetramethyl-, (4aS-cis)-
IUPAC name(7S,9aS)-4,4,7,9a-tetramethyl-1,2,3,6,8,9-hexahydrobenzo[7]annulen-7-ol
SMILESCC1(CCCC2(C1=CCC(CC2)(C)O)C)C
InchiInChI=1S/C15H26O/c1-13(2)7-5-8-14(3)10-11-15(4,16)9-6-12(13)14/h6,16H,5,7-11H2,1-4H3/t14-,15+/m0/s1
FormulaC15H26O
PubChem ID94334
Molweight222.372
LogP3.49
Atoms42
Bonds43
H-bond Acceptor1
H-bond Donor1
Chemical Classificationterpenes alcohols

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaStreptomyces Platensis F-1n/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al., 2008
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2036
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2049
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaStreptomyces Platensis F-1autoclaved wheat seedsHeadspace volatiles from Streptomyces platensis F1 were collected using solid-phase micro extraction (SPME) technique. The volatile compounds produced by 1-week-old cultures grown on autoclaved wheat seeds were identified using 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


Compound Details

Synonymous names
IRAQOCYXUMOFCW-UHFFFAOYSA-N
Cedrene
Cedarwood oil terpenoid
Cedarwood oil terpenes fraction
Cedarwood oil terpenes
Cedarwood oil terpene fraction
Cedarwood oil terpene
AC1LAVA0
Terpene, cedarwood oil
Cedarwood oils, heavy fraction
Terpenes and terpenoids, cedarwood-oil
CTK4E0455
Cedr-8-ene #
PL041404
OR031369
LS-2622
Di-epi-.alpha.-cedrene
KB-18079
DB-025783
FT-0693131
469-61-4
MCULE-9345089020
11028-42-5
19069-48-8
2,6,6,8-TETRAMETHYLTRICYCLO[5.3.1.0(1),?]UNDEC-8-ENE
2,6,6,8-TETRAMETHYLTRICYCLO[5.3.1.0(1,5)]UNDEC-8-ENE
2,6,6,8-Tetramethyl tricyclo[5.3.1.0(1,5)]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.)]-
IUPAC name
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
Molweight204.357
LogP4.1
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiPhoma Sp.n/aplant of L. tridentataStrobel et al., 2011
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2020
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2038
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiPhoma Sp.n/aSolid phase microextraction (SPME)
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


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

Mass-Spectra

Compound Details

Synonymous names
JSNRRGGBADWTMC-NTCAYCPXSA-N
JSNRRGGBADWTMC-UHFFFAOYSA-N
BETA-FARNESENE
trans-beta-Farnesene
AC1NQYKD
beta-trans-farnesene
trans-|A-Farnesene
AC1Q1NVG
trans--Farnesene
trans-beta-Farnesene, analytical standard
E5STW643HU
.beta.-Farnesene
AC1Q2A67
UNII-E5STW643HU
QSPL 026
UNII-4P3OFI15E1 component JSNRRGGBADWTMC-NTCAYCPXSA-N
(E)-beta-farnesene
C09666
DTXSID9047049
LP001693
ZINC1531533
CHEBI:39241
CHEBI:10418
AN-18819
CC-00913
DSSTox_GSID_47049
CJ-24098
MFCD00065433
LMFA11000040
DSSTox_CID_27049
AKOS015913412
FT-0637749
FT-0604961
FT-0604950
I14-46913
Tox21_303792
502-60-3
(Z,E)-.beta.-Farnesene
Ambap18794-84-8
NCGC00357080-01
EINECS 242-582-0
EINECS 278-628-1
18794-84-8
77129-48-7
CAS-18794-84-8
MolPort-006-122-759
1,3(15),6,10-Farnesatetraene
7,11-Dimethyl-3-methylene-1,6E,10-dodecatriene
7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
7,11-Dimethyl-3-methylenedodeca-1,6,10-triene
trans-7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-
(E)-7,11-Dimethyl-3-methylenedodeca-1,6,10-triene
(6E)-7,11-dimethyl-3-methylidenedodeca-1,6,10-triene
(6E)-7,11-dimethyl-3-methylenedodeca-1,6,10-triene
(6E)-7,11-Dimethyl-3-methylene-1,6,10-dodecatriene
(E)-7,11-dimethyl-3-methylene-dodeca-1,6,10-triene
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-, (E)-
1,6,10-Dodecatriene, 7,11-dimethyl-3-methylene-, (6E)-
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
Molweight204.357
LogP5.2
Atoms39
Bonds38
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPenicillium PolonicumPolizzi et al., 2012
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2024
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2041
FungiTrichoderma Atroviride ATCC 74058Stoppacher et al., 2010
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
FungiAspergillus Fumigatuscompost Fischer et al. 2034
FungiTrichoderma AtrovirideCrutcher et al., 2013
FungiTrichoderma ReeseiCrutcher et al., 2013
FungiTrichoderma VirensCrutcher et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPenicillium Polonicummalt 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-MSyes
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)malt extract agarSBSE-GC-MSyes
FungiTrichoderma Atroviride ATCC 74058Potato dextrose agarHS-SPME/GC-MS no
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
FungiAspergillus Fumigatusyest extract sucroseTenax/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


(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


(4aS,7R,7aR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene

Compound Details

Synonymous names
Allo-Aromadendrene
LMPR0103430003
IUPAC name(4aS,7R,7aR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene
SMILESCC1CCC2C1C3C(C3(C)C)CCC2=C
InchiInChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h10-14H,1,5-8H2,2-4H3/t10-,11-,12?,13-,14?/m1/s1
FormulaC15H24
PubChem ID42608158
Molweight204.357
LogP4.15
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
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


(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


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

Compound Details

Synonymous names
Chamigrene
Chamigren
beta-Chamigrene
AC1L9CNQ
(R)-beta-chamigrene
C09637
(-)-chamigrene
CHEBI:10359
(-)-beta-Chamigrene
18431-82-8
(6R)-3,7,7-trimethyl-11-methylidenespiro[5.5]undec-2-ene
(6R)-3,11,11-trimethyl-7-methylidenespiro[5.5]undec-3-ene
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
Molweight204.357
LogP4.53
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62006) Coculture With Fusarium Oxysporum F. Aechmeae(Fr.)Schltdl. (DSMZ 62297)DSMZWeikl et al. 2027
FungiAlternaria Alternata(Fr.)Keissler (DSMZ 62010)DSMZWeikl et al. 2042
FungiPenicillium Decumbensnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
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
FungiPenicillium Decumbensmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiPiptoporus BetulinusnaGC/MSNo


2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-ol

Compound Details

Synonymous names
WMOPMQRJLLIEJV-DOMZBBRYSA-N
epi-Eudesmol
AC1O5B1H
W2237
10-epi-gamma-Eudesmol
SCHEMBL310948
10-epi-?-eudesmol
C19893
CHEBI:62514
ZINC15209455
epi-10- .gamma.-Eudesmol
10alpha-Eudesm-4-en-11-ol
15051-81-7
MolPort-027-637-273
10-epi-eudesm-4-en-11-ol
(-)-10-epi- .gamma.-eudesmol
(2R-trans)-1,2,3,4,4a,5,6,7-Octahydro-alpha,alpha,4a,8-tetramethyl-2-naphthalenemethanol
2-Naphthalenemethanol, 1,2,3,4,4a,5,6,7-octahydro-alpha,alpha,4a,8-tetramethyl-, (2R-trans)-
2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-ol
2-[(2R,4aS)-4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl]propan-2-ol
IUPAC name2-[(2R,4aS)-4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl]propan-2-ol
SMILESCC1=C2CC(CCC2(CCC1)C)C(C)(C)O
InchiInChI=1S/C15H26O/c1-11-6-5-8-15(4)9-7-12(10-13(11)15)14(2,3)16/h12,16H,5-10H2,1-4H3/t12-,15+/m1/s1
FormulaC15H26O
PubChem ID6430754
Molweight222.372
LogP3.43
Atoms42
Bonds43
H-bond Acceptor1
H-bond Donor1
Chemical Classificationterpenes alcohols

mVOC Specific Details


Microorganisms emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
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


(2R)-2,4a,8,8-tetramethyl-1a,3,4,5,6,7-hexahydro-1H-cyclopropa[j]naphthalen-2-ol

Compound Details

Synonymous names
YTLMZAPWDFQBAI-LSPKCOCLSA-N
Thujopsan-2.beta.-ol
IUPAC name(2R)-2,4a,8,8-tetramethyl-1a,3,4,5,6,7-hexahydro-1H-cyclopropa[j]naphthalen-2-ol
SMILESCC1(CCCC2(C13CC3C(CC2)(C)O)C)C
InchiInChI=1S/C15H26O/c1-12(2)6-5-7-13(3)8-9-14(4,16)11-10-15(11,12)13/h11,16H,5-10H2,1-4H3/t11?,13?,14-,15?/m1/s1
FormulaC15H26O
PubChem ID91753211
Molweight222.372
LogP3.2
Atoms42
Bonds44
H-bond Acceptor1
H-bond Donor1
Chemical Classificationterpenes alcohols

mVOC Specific Details


Microorganisms emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
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