Results for:
Species: Fusarium oxysporum MSA 35

Compound Details

Synonymous names
Isolongipholene
Isolongifolene
trans-Isolongifolene
CQUAYTJDLQBXCQ-UHFFFAOYSA-N
AC1L2T2C
(-)-Isolongifoline
PL001072
AN-48692
AKOS015901700
FT-0694511
I14-14688
2,3A-ethanoindan, 3a,4,5,6-tetrahydro-1,1,4,4-tetramethyl-
2,2,7,7-TETRAMETHYLTRICYCLO[6.2.1.0(1),?]UNDEC-5-ENE
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)-
2H-2,4a-Methanonaphthalene, 1,3,4,5,6,7-hexahydro-1,1,5,5-tetramethyl-, (2S-cis)-
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)-
IUPAC name
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
FormulaC15H24
PubChem ID102562
Molweight204.357
LogP4.11
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
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 35long-distance antagonistic actionMinerdi et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/an/a
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSno


(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)


(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene

Mass-Spectra

Compound Details

Synonymous names
ALPHA-CARYOPHYLLENE
Humulene
FAMPSKZZVDUYOS-HRGUGZIWSA-N
alpha-Humulene
alpha-Humalene
AC1NQYKM
alpha-Humulene, analytical standard
.alpha.-Caryophyllene
.alpha.-Humulene
6292AF
54W56MD2WD
CHEMBL251280
UNII-54W56MD2WD
CHEBI:5768
C09684
OR325391
OR031368
LS-58866
DTXSID30858793
ZINC30726967
3,7,10-Humulatriene
MFCD00042689
AKOS015965488
BRN 3240075
FT-0622161
LMPR0103110001
(1E,4E,8E)-alpha-humulene
6753-98-6
EINECS 229-816-7
65907-25-7
19132-75-3
alpha-Humulene, >=96.0% (GC)
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene
2,6,6,9-tetramethyl-cycloundeca-1,4,8-triene
trans,trans,trans-2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene
4-05-00-01171 (Beilstein Handbook Reference)
(E,E,E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene
(1E,4E,8E)-humula-1(11),4,8-triene
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene (E,E,E)-
(1E,4E,8E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene
(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (E,E,E)-
Cycloundeca-1,4,8-triene,2,6,6,9-tetramethyl-, (E,E,E)-
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene-, (1E,4E,8E)-
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-
IUPAC name(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene
SMILESCC1=CCC(C=CCC(=CCC1)C)(C)C
InchiInChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3/b11-6+,13-7+,14-10+
FormulaC15H24
PubChem ID5281520
Molweight204.357
LogP4.88
Atoms39
Bonds39
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes sesquiterpene

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiHypoxylon Antochroum Blacinaendophytic in Bursera lancifoliaUlloa-Benítez et al., 2016
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
FungiPhoma Sp.n/aStrobel et al., 2014
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
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiHypoxylon Antochroum BlaciPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSNo
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiPhoma Sp.n/aSolid phase microextraction (SPME)
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
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSyes
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes


4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane

Compound Details

Synonymous names
FITHEODIIYWPLM-UHFFFAOYSA-N
AC1LBUZB
CTK5J3403
4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane
4,8,8-Trimethyl-2-methylene-4-vinylbicyclo[5.2.0]nonane
4,8,8-Trimethyl-2-methylene-4-vinylbicyclo[5.2.0]nonane #
Bicyclo[5.2.0]nonane, 2-methylene-4,8,8-trimethyl-4-vinyl-
IUPAC name4-ethenyl-4,9,9-trimethyl-6-methylidenebicyclo[5.2.0]nonane
SMILESCC1(CC2C1CCC(CC2=C)(C)C=C)C
InchiInChI=1S/C15H24/c1-6-15(5)8-7-13-12(11(2)9-15)10-14(13,3)4/h6,12-13H,1-2,7-10H2,3-5H3
FormulaC15H24
PubChem ID564746
Molweight204.357
LogP4.48
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
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
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiCU Fusarium Oxysporum Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS


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

Compound Details

Synonymous names
Isocaryophyllene
Caryophyllene
trans-Caryophyllene
gamma-caryophyllene
beta-Caryophyllen
NPNUFJAVOOONJE-FLFDDASRSA-N
L-Caryophyllene
E-Caryophyllene
trans-beta-caryophyllene
AC1NQYKS
NRY8I0KNIR
UNII-NRY8I0KNIR
Caryophyllene (VAN)
beta-Caryophyllene (natural)
(E)-Caryophyllene
BHW853AU9H
.beta.-cis-Caryophyllene
C15H24
UNII-BHW853AU9H
(-)-ISOCARYOPHYLLENE
CHEMBL448700
C09691
CCRIS 8094
CHEBI:5993
OR050747
LS-1865
CARYOPHYLLENE ,ALPHA + BETA MIXT
(-)-E-Caryophyllene
NSC 11906
ZINC30726969
AI3-36121
CARYOPHYLLENE ,ALPHA + BETA MIXT.
FEMA No. 2252
87-44-5
LMPR0103120002
118-65-0
8007-38-3
1407-53-0
EINECS 201-746-1
EINECS 204-267-6
MolPort-000-002-651
1233519-47-5
caryophyllene, (R-(R*,4E,9S))-isomer
2-Methylene-6,10,10-trimethylbicyclo(7.2.0)undec-5-ene
4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene #
8-Methylene-4,11,11-(trimethyl)bicyclo(7.2.0)undec-4-ene
(1beta,9alpha)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undeca-4-ene
(1R,4Z,9S)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
(1R-(1R*,4Z,9S*))-4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene
Bicyclo(7.2.0)undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4Z,9S)-
Bicyclo(7.2.0)undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4E,9S)-
4,11,11-Trimethyl-8-methylenebicyclo(7.2.0)undec-4-ene, (1R-(1R*,4E,9S))-
. E(1/2)-(1R,9S)-8-NC(1/4)x>>u-4,11,11-Ey(1/4)x>>u paragraph signthorn>>.[7.2.0]E(R)O>>Ie-4-I(c)
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*))-
IUPAC name(1R,4Z,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 ID5281522
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSno


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

Compound Details

Synonymous names
NPNUFJAVOOONJE-QWAJQTJBSA-N
9-epi-trans-Caryophyllene
AC1O57UK
epi-.beta.-Caryophyllene
C20478
beta-Caryophyllene (1)
BDBM113763
CHEBI:68667
9-epi-.beta.-Caryophyllene
ZINC49538667
9-epi-(E)-caryophyllene
2-epi-(E)-beta-Caryophyllene
(E)-2-epi-beta-caryophyllene
(−)-trans-Caryophyllene
(+)-9-epi-.beta.-Caryophyllene
(1R,9R,E)-4,11,11-Trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene
(1R,4E,9R)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, (1R,4E,9R)-
Bicyclo[7.2.0]undec-4-ene, 4,11,11-trimethyl-8-methylene-, [1R-(1R*,4E,9R*)]-
IUPAC name(1R,4E,9R)-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+/m0/s1
FormulaC15H24
PubChem ID6429274
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
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
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS