Results for:
Species: Streptomyces platensis

1-(3-methylphenyl)ethanone

Mass-Spectra

Compound Details

Synonymous names
3'-Methylacetophenone
585-74-0
1-(m-Tolyl)ethanone
3-METHYLACETOPHENONE
m-Methylacetophenone
Ethanone, 1-(3-methylphenyl)-
1-(3-Methylphenyl)ethanone
Acetophenone, m-methyl-
Acetophenone, 3'-methyl-
1-m-tolylethanone
1-m-Tolyl-ethanone
V3KL17Y68N
MFCD00008742
NSC-46632
Methyl m-tolyl ketone
1-[3-methylphenyl]ethanone
3-Acetyltoluene
1-(3-methylphenyl)-Ethanone
1-(3-methylphenyl)ethan-1-one
UNII-V3KL17Y68N
EINECS 209-561-8
NSC 46632
3'-methyl acetophenone
3\'-Methylacetophenone
3 inverted exclamation marka-Methylacetophenone
SCHEMBL76212
3'-Methylacetophenone, 98%
1-(3-Methylphenyl)ethanone #
DTXSID5074717
CHEBI:178621
NSC46632
STL183829
AKOS009031466
AC-3644
CS-W013375
MCULE-9520106797
SY049547
DB-053228
AM20040783
M0191
NS00033963
EN300-20807
3 inverted exclamation mark -Methylacetophenone
A19719
W-105383
Q27291491
F0001-1527
Z104482920
InChI=1/C9H10O/c1-7-4-3-5-9(6-7)8(2)10/h3-6H,1-2H
Microorganism:

Yes

IUPAC name1-(3-methylphenyl)ethanone
SMILESCC1=CC(=CC=C1)C(=O)C
InchiInChI=1S/C9H10O/c1-7-4-3-5-9(6-7)8(2)10/h3-6H,1-2H3
FormulaC9H10O
PubChem ID11455
Molweight134.17
LogP2.3
Atoms10
Bonds1
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids aromatic compounds aromatic ketones ketones
CHEBI-ID178621
Supernatural-IDSN0094480

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus Versicolorn/aNAFischer et al. 1999
EukaryotaAspergillus Versicolorcompost Fischer et al. 1999
ProkaryotaStreptomyces Platensisn/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus Versicoloryeast extract sucrose agarn/ano
EukaryotaAspergillus Versicoloryest extract sucroseTenax/GC-MSno
ProkaryotaStreptomyces Platensisautoclaved 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.no


2,5-ditert-butylphenol

Mass-Spectra

Compound Details

Synonymous names
2,5-Di-tert-butylphenol
5875-45-6
2,5-ditert-butylphenol
Phenol, 2,5-bis(1,1-dimethylethyl)-
Phenol, 2,5-di-tert-butyl-
2,5-bis(1,1-Dimethylethyl)phenol
R9R0A277K1
NSC-68767
UNII-R9R0A277K1
NSC68767
EINECS 227-543-8
NSC 68767
2,5-di-t-butyl phenol
3,6-di-tert-butylphenol
2,5-di-tert-butyl-phenol
NCIOpen2_003366
SCHEMBL142987
CHEMBL1795399
DTXSID0064046
CHEBI:143859
MFCD00233163
AKOS016347308
MCULE-3858730472
2,5-DI-TERT-BUTYLHYDROXYBENZENE
CS-0364969
NS00020433
AG-672/25002578
Q27288018
Microorganism:

Yes

IUPAC name2,5-ditert-butylphenol
SMILESCC(C)(C)C1=CC(=C(C=C1)C(C)(C)C)O
InchiInChI=1S/C14H22O/c1-13(2,3)10-7-8-11(12(15)9-10)14(4,5)6/h7-9,15H,1-6H3
FormulaC14H22O
PubChem ID79983
Molweight206.32
LogP4.9
Atoms15
Bonds2
H-bond Acceptor1
H-bond Donor1
Chemical Classificationaromatic compounds phenols benzenoids
CHEBI-ID143859
Supernatural-IDSN0182328

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaCandida AlbicansNAKarami et al. 2017
ProkaryotaEscherichia ColiNAKarami et al. 2017
EukaryotaCryptococcus Sp.inhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaVishniacozyma Victoriaeinhibitory and promoting effects on the growth of different microorganismsisolate from Dryas octopetala, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
EukaryotaMrakia Gelidainhibitory and promoting effects on the growth of different microorganismsisolate from Saxifraga cespitosa, Ny-Ålesund (Svalbard Archipelago, Arctic); CCTCC (China Center for Type Culture Collection, Wuhan, Hubei, China)Niu et al. 2022
ProkaryotaStreptomyces Platensisn/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al. 2008
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaCandida AlbicansMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
ProkaryotaEscherichia ColiMueller Hinton broth (MB), tryptic soy broth (TSB)SPME, DVB/CAR/PDMS, GC-MSno
EukaryotaCryptococcus Sp.artificial nectar mediaGC-MSno
EukaryotaVishniacozyma Victoriaeartificial nectar mediaGC-MSno
EukaryotaMrakia Gelidaartificial nectar mediaGC-MSno
ProkaryotaStreptomyces Platensisautoclaved 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.no
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno


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

Compound Details

Synonymous names
1H-Benzocyclohepten-7-ol, 2,3,4,4a,5,6,7,8-octahydro-1,1,4a.alpha.,7.beta.-tetramethyl-
1H-Benzocyclohepten-7-ol, 2,3,4,4a,5,6,7,8-octahydro-1,1,4a,7-tetramethyl-, cis-
1,1,4a,7-Tetramethyl-2,3,4,4a,5,6,7,8-octahydro-1H-benzo[a]cyclohepten-7-ol #
BXGVVQADPFXGHD-YSSOQSIOSA-N
Microorganism:

Yes

IUPAC name(7S)-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-/m1/s1
FormulaC15H26O
PubChem ID5315300
Molweight222.37
LogP4.1
Atoms16
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationterpenes alcohols
Supernatural-IDSN0037987-03

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces Platensisn/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Platensisautoclaved 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.no


Methyl 2-methylbutanoate

Mass-Spectra

Compound Details

Synonymous names
Methyl 2-methylbutyrate
868-57-5
METHYL 2-METHYLBUTANOATE
Butanoic acid, 2-methyl-, methyl ester
METHYL2-METHYLBUTYRATE
Methyl DL-2-Methylbutyrate
Methyl (S)-2-Methylbutanoate
Butyric acid, 2-methyl-, methyl ester
2-Methylbutyric acid methyl ester
FEMA No. 2719
Methyl anteisovalerate
dl-2-Methylbutyric acid methyl ester
Methyl .alpha.-methylbutyrate
Methyl .alpha.-methylbutanoate
OLG4D4939V
DTXSID1052587
CHEBI:88538
(+/-)-Methyl 2-methylbutanoate
2-Methylbutyric acid-methyl ester
DL-2-MethylbutyricAcidMethyl-d3Ester
Butyric acid, .alpha.-methyl-, methyl ester
methyl 2-methyl butyrate
1082582-07-7
53955-81-0
Methyl alpha-methylbutyrate
Methyl alpha-methylbutanoate
UNII-OLG4D4939V
Methyl 2-methylbutyrate (natural)
2-methylbutanoic acid methyl ester
EINECS 212-778-0
AI3-34461
SCHEMBL108113
Methyl 2-methylbutyrate, 99%
(+/-)-Methyl a-methylbutyrate
CHEMBL2287316
DTXCID2031160
FEMA 2719
a-Methylbutyric acid methyl ester
Methyl (+/-)-2-methylbutanoate
2-Methylbutyric acid, methyl ester
2-methyl-butanoic acid methyl ester
2-Methylbutanoic acid, methyl ester
Tox21_303742
LMFA07010934
MFCD00009335
AKOS009117977
alpha-methyl-butyric acid methyl ester
METHYL 2-METHYLBUTYRATE [FCC]
FS-3839
METHYL 2-METHYLBUTYRATE [FHFI]
Methyl ester of 2-methyl-butanoic acid
METHYL DL-.ALPHA.-METHYLBUTYRATE
NCGC00357048-01
CAS-868-57-5
DB-056956
CS-0132254
M0758
Methyl 2-methylbutyrate, >=98%, FCC, FG
Methyl 2-methylbutyrate, analytical standard
NS00012916
(+/-)-METHYL .ALPHA.-METHYLBUTYRATE
.ALPHA.-METHYLBUTYRIC ACID METHYL ESTER
E75864
EN300-254095
Butanoic acid, 2-methyl-, methyl ester, ( )-
Butanoic acid, 2-methyl-, methyl ester, (plusmn)-
Butanoic acid, 2-methyl-, methyl ester, (.+/-.)-
Methyl 2-methylbutyrate, natural, >=98%, FCC, FG
Q24734848
Microorganism:

Yes

IUPAC namemethyl 2-methylbutanoate
SMILESCCC(C)C(=O)OC
InchiInChI=1S/C6H12O2/c1-4-5(2)6(7)8-3/h5H,4H2,1-3H3
FormulaC6H12O2
PubChem ID13357
Molweight116.16
LogP1.5
Atoms8
Bonds3
H-bond Acceptor2
H-bond Donor0
Chemical Classificationesters
CHEBI-ID88538
Supernatural-IDSN0261979

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas AeruginosaNANAFitzgerald et al. 2021
ProkaryotaPseudomonas AeruginosaNANAFilipiak et al. 2012
ProkaryotaMycobacterium BovisNANAMcNerney et al. 2012
ProkaryotaLysobacter Capsiciantifungal activity against the growth of Pythium ultimum, Rhizoctonia solani and Sclerotinia minorNAVlassi et al. 2020
EukaryotaTuber AestivumBurgundy regionMolinier et al. 2015
EukaryotaEmericella Nidulansn/aNAFischer et al. 1999
EukaryotaXylaria Sp.naHaematoxylon brasiletto, Morelos, MexicoSánchez-Ortiz et al. 2016
ProkaryotaStreptomyces Albusn/aNASchöller et al. 2002
ProkaryotaStreptomyces Antibioticusn/aNASchöller et al. 2002
ProkaryotaStreptomyces Aureofaciensn/aNASchöller et al. 2002
ProkaryotaStreptomyces Coelicolorn/aNASchöller et al. 2002
ProkaryotaStreptomyces Griseusn/aNASchöller et al. 2002
ProkaryotaStreptomyces Hygroscopicusn/aNASchöller et al. 2002
ProkaryotaStreptomyces Murinusn/aNASchöller et al. 2002
ProkaryotaStreptomyces Thermoviolaceusn/aNASchöller et al. 2002
EukaryotaTuber Melanosporumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Mesentericumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Rufumn/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
EukaryotaTuber Simonean/aAyme Truffe of Grignan, 26230 FranceMarch et al. 2006
ProkaryotaStreptomyces Platensisn/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al. 2008
ProkaryotaActinomycetes Sp.n/aNASchulz and Dickschat 2007
ProkaryotaCollimonas Pratensisn/aNAGarbeva et al. 2014
ProkaryotaCollimonas Pratensisnarhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al. 2014
EukaryotaTuber MesentericumNoneNoneMarch et al. 2006
EukaryotaMetschnikowia HawaiiensisNANALjunggren et al. 2019
EukaryotaCryptococcus WieringaeNANAMozūraitis et al. 2022
Lentinula EdodesGeng et al. 2024
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas AeruginosaLBSPME/GC-MSno
ProkaryotaPseudomonas AeruginosaTSBSPME/GC-MSno
ProkaryotaPseudomonas Aeruginosatryptic soy brothTD/GC-MSno
ProkaryotaMycobacterium BovisLG + glycerolTD/GC-MS and SIFT-MSno
ProkaryotaLysobacter CapsiciNA-mediaGC-MSno
EukaryotaTuber AestivumHS-SPME/GC-MS yes
EukaryotaEmericella Nidulansyeast extract sucrose agarn/ano
EukaryotaXylaria Sp.PDA mediumSPME-GC/MSyes
ProkaryotaStreptomyces Albusn/an/ano
ProkaryotaStreptomyces Antibioticusn/an/ano
ProkaryotaStreptomyces Aureofaciensn/an/ano
ProkaryotaStreptomyces Coelicolorn/an/ano
ProkaryotaStreptomyces Griseusn/an/ano
ProkaryotaStreptomyces Hygroscopicusn/an/ano
ProkaryotaStreptomyces Murinusn/an/ano
ProkaryotaStreptomyces Thermoviolaceusn/an/ano
EukaryotaTuber Melanosporumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Mesentericumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Rufumn/aPressure balanced head-space sampling and GC/TOF-MSno
EukaryotaTuber Simonean/aPressure balanced head-space sampling and GC/TOF-MSno
ProkaryotaStreptomyces Platensisautoclaved 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.no
ProkaryotaActinomycetes Sp.n/an/ano
ProkaryotaCollimonas PratensisHeadspace trapping/GC-MSno
ProkaryotaCollimonas Pratensissand containing artificial root exudatesGC/MSno
EukaryotaTuber MesentericumNonePressure balanced head-space sampling and GC/TOF-MSno
EukaryotaMetschnikowia Hawaiiensisliquid YPD mediumGC-MSno
EukaryotaCryptococcus WieringaeYPD-agar plates (1% yeast extract, 1% peptone, 2% dextrose, 2% agar)SPME-GC-MSno
Lentinula EdodesJiuqu (traditional wheat Qu)GC-IMSno


Methyl Cyclohexanecarboxylate

Mass-Spectra

Compound Details

Synonymous names
Methyl cyclohexanecarboxylate
4630-82-4
Methyl cyclohexanoate
Hexahydrobenzoic acid methyl ester
CYCLOHEXANECARBOXYLIC ACID, METHYL ESTER
Methyl cyclohexylcarboxylate
Methyl hexahydrobenzoate
Cyclohexanecarboxylic Acid Methyl Ester
Methyl cyclohexylformate
FEMA No. 3568
methylcyclohexanecarboxylate
CyclohexanecarboxylicAcidMethylEster-d11
Methyl ester of cyclohexanecarboxylic acid
96144H696Q
methyl cyclohexane carboxylate
vanilla carboxylate
EINECS 225-050-2
BRN 1306359
AI3-04803
UNII-96144H696Q
methyl cyclohexancarboxylate
c-C6H11COOCH3
methylcyclohexane carboxylate
SCHEMBL18552
methyl cyclohexane-carboxylate
methyl-cyclohexane carboxylate
4-09-00-00017 (Beilstein Handbook Reference)
DTXSID9074303
CHEBI:88845
FEMA 3568
Methyl cyclohexanecarboxylate, 98%
MFCD00001458
s6299
AKOS008903582
Methyl cyclohexanecarboxylate, >=98%
CS-W007704
HY-W007704
MCULE-6850082589
Cyclohexane carboxylic acid methyl ester
cyclohexane-carboxylic acid methyl ester
cyclohexane carboxylic acid, methyl ester
AS-13138
DB-051370
METHYL CYCLOHEXANECARBOXYLATE [FHFI]
NS00022207
D77686
EN300-130684
A827025
W-106094
Q27160838
Z18267125
InChI=1/C8H14O2/c1-10-8(9)7-5-3-2-4-6-7/h7H,2-6H2,1H
Microorganism:

Yes

IUPAC namemethyl cyclohexanecarboxylate
SMILESCOC(=O)C1CCCCC1
InchiInChI=1S/C8H14O2/c1-10-8(9)7-5-3-2-4-6-7/h7H,2-6H2,1H3
FormulaC8H14O2
PubChem ID20748
Molweight142.2
LogP2.2
Atoms10
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationesters
CHEBI-ID88845
Supernatural-IDSN0477873

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStreptomyces Platensisn/aS. platensis F-1 was isolated from a healthy plant of rice (Oryza sativa).Wan et al. 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStreptomyces Platensisautoclaved 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.no