Results for:
Species: Algihabitans albus

2,5-di(propan-2-yl)pyrazine

Compound Details

Synonymous names
2,5-diisopropylpyrazine
24294-83-5
2,5-di(propan-2-yl)pyrazine
2,5-Diisopropyl-pyrazine
2,5-bis(propan-2-yl)pyrazine
SCHEMBL5950443
CHEBI:199215
LXJYUERPFWUCNN-UHFFFAOYSA-N
AKOS006370977
AB93060
CS-0449966
InChI=1/C10H16N2/c1-7(2)9-5-12-10(6-11-9)8(3)4/h5-8H,1-4H
Microorganism:

Yes

IUPAC name2,5-di(propan-2-yl)pyrazine
SMILESCC(C)C1=CN=C(C=N1)C(C)C
InchiInChI=1S/C10H16N2/c1-7(2)9-5-12-10(6-11-9)8(3)4/h5-8H,1-4H3
FormulaC10H16N2
PubChem ID11491990
Molweight164.25
LogP2.1
Atoms12
Bonds2
H-bond Acceptor2
H-bond Donor0
Chemical Classificationaromatic compounds nitrogen compounds heterocyclic compounds pyrazines
CHEBI-ID199215
Supernatural-IDSN0218015

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaSphingopyxis Litorisisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaChondromyces CrocatusIs an attractant of Carpophilus beetles.NASchulz et al. 2004
ProkaryotaNannocystis Exedensn/aNADickschat et al. 2007
ProkaryotaChondromyces Crocatusn/aNADickschat et al. 2005_6
ProkaryotaPaenibacillus PolymyxaThis compound is an attractant of the pineapple beetle Carpophilus humeralis.NASchulz and Dickschat 2007
ProkaryotaChondromyces CrocatusThis compound is an attractant of the pineapple beetle Carpophilus humeralis.NASchulz and Dickschat 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaSphingopyxis Litorismarine broth agarOSSA/GC-MSno
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno
ProkaryotaChondromyces Crocatusn/an/ano
ProkaryotaNannocystis Exedensn/an/ano
ProkaryotaPaenibacillus Polymyxan/an/ano


Cyclohex-3-ene-1-carbonitrile

Compound Details

Synonymous names
100-45-8
3-Cyclohexene-1-carbonitrile
4-Cyano-1-cyclohexene
4-Cyanocyclohexene
cyclohex-3-enecarbonitrile
3-Cyclohexenecarbonitrile
3-Cyclohexenyl cyanide
1-Cyano-3-cyclohexene
cyclohex-3-ene-1-carbonitrile
Cyclohex-3-enenitrile
3-Cyklohexenylkyanid
D65GN9AVCH
NSC-7407
3-Cyklohexenylkyanid [Czech]
4-Cyanocyclohexene-1
1,2,5,6-Tetrahydrobenzonitrile
NSC 7407
UNII-D65GN9AVCH
BRN 0636074
AI3-08635
NSC7407
Tetrahydrobenzonitrile
4-Cyclohexenecarbonitrile
WLN: L6UTJ DCN
4-09-00-00116 (Beilstein Handbook Reference)
SCHEMBL167234
3-aCyclohexene-a1-acarbonitrile
1,2,3,6-Tetrahydrobenzonitrile
DTXSID70861706
MFCD00013778
AKOS006229199
AS-47878
NS00096253
(+/-)-3-CYCLOHEXENE-1-CARBONITRILE
F16653
Q22079568
Microorganism:

Yes

IUPAC namecyclohex-3-ene-1-carbonitrile
SMILESC1CC(CC=C1)C#N
InchiInChI=1S/C7H9N/c8-6-7-4-2-1-3-5-7/h1-2,7H,3-5H2
FormulaC7H9N
PubChem ID66013
Molweight107.15
LogP1.5
Atoms8
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationnitriles nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaSphingopyxis Litorisisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaLitoreibacter Sp.isolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaSphingopyxis Litorismarine broth agarOSSA/GC-MSno
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno
ProkaryotaLitoreibacter Sp.marine broth agarOSSA/GC-MSno


N-(2-methylpropyl)propanamide

Compound Details

Synonymous names
n-isobutylpropionamide
5827-75-8
N-(2-methylpropyl)propanamide
Propanamide, N-isobutyl
MFCD01345651
NSC406183
NCIOpen2_003731
SCHEMBL564899
DTXSID50324268
QTVUDNOFBZLOHM-UHFFFAOYSA-N
AC2518
AKOS003852810
NSC-406183
CS-11986
DA-42026
SY034683
CS-0152594
A869487
Microorganism:

Yes

IUPAC nameN-(2-methylpropyl)propanamide
SMILESCCC(=O)NCC(C)C
InchiInChI=1S/C7H15NO/c1-4-7(9)8-5-6(2)3/h6H,4-5H2,1-3H3,(H,8,9)
FormulaC7H15NO
PubChem ID347479
Molweight129.2
LogP1.3
Atoms9
Bonds3
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamides nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno


N-(2-methylbutyl)acetamide

Compound Details

Synonymous names
n-(2-methylbutyl)acetamide
54824-90-7
N-(2-methylbutyl)-acetamide
Acetamide, N-(2-methylbutyl)-
NSC156658
SCHEMBL799657
Acetamide, N-(2-methylbutyl)
DTXSID20303106
UBERLXYRZNEDEB-UHFFFAOYSA-N
AKOS006359579
NSC-156658
Microorganism:

Yes

IUPAC nameN-(2-methylbutyl)acetamide
SMILESCCC(C)CNC(=O)C
InchiInChI=1S/C7H15NO/c1-4-6(2)5-8-7(3)9/h6H,4-5H2,1-3H3,(H,8,9)
FormulaC7H15NO
PubChem ID291446
Molweight129.2
LogP1.2
Atoms9
Bonds3
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamides nitrogen compounds

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno


N-(2-methylpropyl)acetamide

Mass-Spectra

Compound Details

Synonymous names
N-(2-Methylpropyl)acetamide
N-Isobutylacetamide
1540-94-9
N-(2-Methyl-2-propyl)ethanamide
N-Acetyl-2-methyl-1-propaneamine
Acetamide, N-isobutyl-
Acetamide, N-(2-methylpropyl)-
N-Isobutyl-Acetamide
03RBP530AC
NSC-156655
UNII-03RBP530AC
Acetylisobutylamine
NSC156655
SCHEMBL91326
N-(2-Methylpropyl)-Acetamide
N-(2-Methyl-propyl)ethanamide
DTXSID90165516
CHEBI:179639
VDQMVRFHUYAKJL-UHFFFAOYSA-N
N-(2-Methylpropyl)acetamide, 9CI
AKOS003855864
NSC 156655
Q27247578
Microorganism:

Yes

IUPAC nameN-(2-methylpropyl)acetamide
SMILESCC(C)CNC(=O)C
InchiInChI=1S/C6H13NO/c1-5(2)4-7-6(3)8/h5H,4H2,1-3H3,(H,7,8)
FormulaC6H13NO
PubChem ID137071
Molweight115.17
LogP0.9
Atoms8
Bonds2
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamides nitrogen compounds
CHEBI-ID179639
Supernatural-IDSN0387515

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaSphingopyxis Litorisisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaStreptomyces Sp.NAJones et al. 2017
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaSphingopyxis Litorismarine broth agarOSSA/GC-MSno
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno
ProkaryotaStreptomyces Sp.YPD agarGCxGC-TOFMSno


N-(3-methylbutyl)acetamide

Mass-Spectra

Compound Details

Synonymous names
N-(3-Methylbutyl)acetamide
N-Isopentylacetamide
13434-12-3
Acetamide, N-(3-methylbutyl)-
n-(iso-pentyl)acetamide
B07X8XNE8T
NSC-156656
UNII-B07X8XNE8T
NSC 156656
NSC156656
n-3-methylbutylacetamide
AI3-35871
N-(3Metylbutiyl) Acetamide
SCHEMBL800814
DTXSID10158662
CHEBI:166455
MFCD00043542
AKOS003799421
CS-0334392
Q27274221
Microorganism:

Yes

IUPAC nameN-(3-methylbutyl)acetamide
SMILESCC(C)CCNC(=O)C
InchiInChI=1S/C7H15NO/c1-6(2)4-5-8-7(3)9/h6H,4-5H2,1-3H3,(H,8,9)
FormulaC7H15NO
PubChem ID98643
Molweight129.2
LogP1.2
Atoms9
Bonds3
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamides nitrogen compounds
CHEBI-ID166455
Supernatural-IDSN0441686

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaSphingopyxis Litorisisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaCoraliitalea Coraliiisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaStigmatella Aurantiacan/aNASchulz and Dickschat 2007
ProkaryotaStreptomyces Sp.NAJones et al. 2017
ProkaryotaStigmatella Aurantiacan/aNADickschat et al. 2005_5
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaSphingopyxis Litorismarine broth agarOSSA/GC-MSno
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno
ProkaryotaCoraliitalea Coraliimarine broth agarOSSA/GC-MSno
ProkaryotaStigmatella Aurantiacan/an/ano
ProkaryotaStreptomyces Sp.YPD agarGCxGC-TOFMSno


(E)-1-(2,6,6-trimethylcyclohex-2-en-1-yl)pent-1-en-3-one

Compound Details

Synonymous names
Ionone, methyl-
Methyl ionone
6-Methylionone
1335-46-2
1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one
alpha-methyl ionone
7779-30-8
alpha-Cetone
(E)-1-(2,6,6-trimethylcyclohex-2-en-1-yl)pent-1-en-3-one
1-(2,6,6-trimethylcyclohex-2-en-1-yl)pent-1-en-3-one
1322-70-9
alpha-Methylionone
1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one
Methyl-alpha-ionone
1-PENTEN-3-ONE, 1-(2,6,6-TRIMETHYL-2-CYCLOHEXEN-1-YL)-
5-(2,6,6-Trimethyl-2-cyclohexenyl)-4-penten-3-one
FEMA No. 2711
(e)-1-(2,6,6-trimethylcyclohex-2-enyl)pent-1-en-3-one
1-(2,6,6-Trimethyl-2-cyclohexene-1-yl)-1-penten-3-one
(1E)-1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one
Cetone, alpha-
Methylionone, alpha-
127-42-4
A-METHYLIONONE
1-Penten-3-one, 1-((1R)-2,6,6-trimethyl-2-cyclohexen-1-yl)-, (1E)-
EINECS 204-842-1
EINECS 215-635-0
EINECS 231-926-5
DTXSID6026240
NSC 163996
Methyl-Ionone
Methyl ionone 3
N-Methyl-a-ionone
1-Methyl-a-ionone
.alpha.-N-Methyl ionone
DSSTox_CID_6240
EC 215-635-0
DSSTox_RID_78712
DSSTox_GSID_29214
DTXCID206240
CHEMBL1371285
FEMA 2711
VPKMGDRERYMTJX-CMDGGOBGSA-
CHEBI:172145
DTXSID501197970
Tox21_201192
Tox21_301465
(R-(E))-1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)pent-1-en-3-one
1-Penten-3-one, 1-(2,6,6-trimethyl-2-cyclohexen-1-yl)- (VAN)
NSC163996
1-Penten-3-one, 1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-, (theta-(E))-
HY-W355140
NSC-163996
1-2,6,6-Trimethylcyclohex-2-en-1-yl
NCGC00091848-01
NCGC00091848-02
NCGC00091848-03
NCGC00255231-01
NCGC00258744-01
CAS-1335-46-2
CAS-7779-30-8
CS-0466424
NS00006735
Q3920656
W-108297
W-110238
1-2,6,6-Trimethylcyclohex-2-en-1-yl;pent-1-en-3-one
1-(2,6,6-Trimethylcyclohex-2-en-1-yl)-1-pentene-3-one
1-Penten-3-one,6,6-trimethyl-2-cyclohexen-1-yl)- (VA
4-Penten-3-one,5-(2,6,6-trimethyl-2-cyclohexen-1-yl)
(1E)-1-(2,6,6-trimethylcyclohex-2-en-1-yl)pent-1-en-3-one
Methylionone (mixture of |A- and |A-, predominantly |A-n-isomer)
InChI=1/C14H22O/c1-5-12(15)8-9-13-11(2)7-6-10-14(13,3)4/h7-9,13H,5-6,10H2,1-4H3/b9-8+
Microorganism:

Yes

IUPAC name(E)-1-(2,6,6-trimethylcyclohex-2-en-1-yl)pent-1-en-3-one
SMILESCCC(=O)C=CC1C(=CCCC1(C)C)C
InchiInChI=1S/C14H22O/c1-5-12(15)8-9-13-11(2)7-6-10-14(13,3)4/h7-9,13H,5-6,10H2,1-4H3/b9-8+
FormulaC14H22O
PubChem ID5371084
Molweight206.32
LogP3.4
Atoms15
Bonds3
H-bond Acceptor1
H-bond Donor0
Chemical Classificationterpenes ketones
CHEBI-ID172145
Supernatural-IDSN0396564-01

mVOC Specific Details

Boiling Point
DegreeReference
238 median

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaAspergillus NigerNANACosta et al. 2016
EukaryotaCandida AlbicansNANACosta et al. 2016
EukaryotaPenicillium ChrysogenumNANACosta et al. 2016
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
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaAspergillus NigerYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaCandida AlbicansYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaPenicillium ChrysogenumYeast Glucose ChloramphenicolSPME/GCxGC-MSno
EukaryotaCandida AlbicansYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida GlabrataYGC mediaHS-SPME/GC-GC-ToFMSno
EukaryotaCandida TropicalisYGC mediaHS-SPME/GC-GC-ToFMSno
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno


Cyclohepta-2,4,6-trien-1-one

Mass-Spectra

Compound Details

Synonymous names
Tropone
539-80-0
cyclohepta-2,4,6-trien-1-one
2,4,6-CYCLOHEPTATRIEN-1-ONE
Cycloheptatrienone
Tropon
2,4,6-Cycloheptatriene-1-one
CO48X7SUFH
MFCD00014331
UNII-CO48X7SUFH
cyclohepta-2,4,6-trienone
EINECS 208-725-6
Tropone, 97%
2,4,6-cycloheptatrienone
SCHEMBL316824
2,4,6-cycloheptatrien-1-on
1-cyclohepta-2,4,6-trienone
SCHEMBL18727723
DTXSID60202169
2,4,6-CYCLOHEPTATRIN-1-ONE
AKOS024365345
HY-W035904
MCULE-5628531135
(2Z,4Z,6Z)-cyclohepta-2,4,6-trienone
DB-052444
CS-0088241
NS00043109
D74673
A829875
Q413630
doi:10.14272/QVWDCTQRORVHHT-UHFFFAOYSA-N.1
InChI=1/C7H6O/c8-7-5-3-1-2-4-6-7/h1-6
Microorganism:

Yes

IUPAC namecyclohepta-2,4,6-trien-1-one
SMILESC1=CC=CC(=O)C=C1
InchiInChI=1S/C7H6O/c8-7-5-3-1-2-4-6-7/h1-6H
FormulaC7H6O
PubChem ID10881
Molweight106.12
LogP1.6
Atoms8
Bonds0
H-bond Acceptor1
H-bond Donor0
Chemical Classificationalkenes ketones cycloalkenes

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaCoraliitalea Coraliiisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
ProkaryotaArthrobacter Agilisnarhizosphere of maize plantsVelázquez-Becerra et al. 2011
ProkaryotaLoktanella Sp.n/aNASchulz and Dickschat 2007
ProkaryotaAzoarcus Evansiin/aNASchulz and Dickschat 2007
ProkaryotaLoktanella Sp.n/aNADickschat et al. 2005_4
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno
ProkaryotaCoraliitalea Coraliimarine broth agarOSSA/GC-MSno
ProkaryotaArthrobacter AgilisLB mediumSPME-GC/MSno
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaAzoarcus Evansiin/an/ano


2-hydroxycyclohepta-2,4,6-trien-1-one

Compound Details

Synonymous names
Tropolone
533-75-5
2-Hydroxycyclohepta-2,4,6-trienone
Purpurocatechol
2-hydroxycyclohepta-2,4,6-trien-1-one
2-Hydroxy-2,4,6-cycloheptatrien-1-one
2,4,6-Cycloheptatrien-1-one, 2-hydroxy-
2-Hydroxytropone
2-Hydroxy-2,4,6-cycloheptatrienone
MFCD00004158
NSC89303
2-Hydroxy-2,4,6-cycloheptatriene-1-one
7L6DL16P1T
CHEMBL121188
DTXSID8049416
CHEBI:79966
NSC-89303
CCRIS 6609
EINECS 208-577-2
NSC 89303
BRN 1904978
UNII-7L6DL16P1T
Tropomyosins
0TR
Tropolone, 98%
TROPOLONE [MI]
TROPOLONE [INCI]
.ALPHA.-TROPOLONE
NCIMech_000829
TROPOLONE [WHO-DD]
SCHEMBL42739
4-08-00-00159 (Beilstein Handbook Reference)
DTXCID7029376
SCHEMBL14016544
HY-N7135
Tox21_202924
AC1614
BDBM50236983
CCG-35867
s5688
2-Hydroxy-cyclohepta-2,4,6-trienone
AKOS015900394
Tropolone, purum, >=98.0% (GC)
CS-W013560
MCULE-1658872761
2,6-Cycloheptatrien-1-one, 2-hydroxy-
NCGC00260470-01
AC-25757
AS-14018
CAS-533-75-5
NCI60_041986
SY009930
2-hydroxy-2,4,6-cycloheptatrien -1-one
DB-052324
NS00032738
T0606
EN300-124250
(2E,4Z,6Z)-2-hydroxycyclohepta-2,4,6-trienone
A829552
W-105743
Q19952843
F0001-1377
InChI=1/C7H6O2/c8-6-4-2-1-3-5-7(6)9/h1-5H,(H,8,9
Microorganism:

Yes

IUPAC name2-hydroxycyclohepta-2,4,6-trien-1-one
SMILESC1=CC=C(C(=O)C=C1)O
InchiInChI=1S/C7H6O2/c8-6-4-2-1-3-5-7(6)9/h1-5H,(H,8,9)
FormulaC7H6O2
PubChem ID10789
Molweight122.12
LogP0.5
Atoms9
Bonds0
H-bond Acceptor2
H-bond Donor1
Chemical Classificationketones alcohols
CHEBI-ID79966
Supernatural-IDSN0222999

mVOC Specific Details

Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaAlgihabitans Albusisolate from the algal Chromera velia CCAP 1602/1Koteska et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaAlgihabitans Albusmarine broth agarOSSA/GC-MSno