U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C15H24
Molecular Weight 204.3511
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALENCENE

SMILES

C[C@@H]1CCC=C2CC[C@H](C[C@@]12C)C(C)=C

InChI

InChIKey=QEBNYNLSCGVZOH-NFAWXSAZSA-N
InChI=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+/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Germacrene A is a product of the aristolochene synthase-mediated conversion of farnesylpyrophosphate to aristolochene.
2002 Oct 2
Structure-activity of valencenoid derivatives and their repellence to the Formosan subterranean termite.
2003 Dec
Citrus fruit flavor and aroma biosynthesis: isolation, functional characterization, and developmental regulation of Cstps1, a key gene in the production of the sesquiterpene aroma compound valencene.
2003 Dec
Volatiles from leaves, fruits, and virgin oil from Olea europaea Cv. Olivastra Seggianese from Italy.
2003 Feb 26
Monitoring and fast detection of mycotoxin-producing fungi based on headspace solid-phase microextraction and headspace sorptive extraction of the volatile metabolites.
2003 Jan 24
The sesquiterpenoid nootkatone and the absolute configuration of a dibromo derivative.
2003 May
Highly efficient production of nootkatone, the grapefruit aroma from valencene, by biotransformation.
2005 Nov
Analysis of the essential oil composition from the different parts of Eryngiumglaciale Boiss. from Spain.
2005 Nov 11
Headspace solid-phase microextraction-gas chromatography--mass spectrometry analysis of the volatile compounds of Evodia species fruits.
2005 Sep 16
Valence isomerization of 2-phospha-4-silabicyclo[1.1.0]butane: a high-level ab initio study.
2006 Jul
[Increase of copy number of HMG-CoA reductase and FPP synthase genes improves the amorpha4,11-diene production in engineered yeast].
2007 Dec
Chemical composition of the essential oil of Pelargonium quercetorum Agnew. of Iran.
2007 Jan
[GC-MS analysis of volatile constituents from five different kinds of Chinese eaglewood].
2007 May
Production of plant sesquiterpenes in Saccharomyces cerevisiae: effect of ERG9 repression on sesquiterpene biosynthesis.
2008 Feb 15
Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling.
2008 Jan
Essential Oil Composition and Antibacterial Studies of Vitex negundo Linn. Extracts.
2008 Jul-Aug
Regioselective biooxidation of (+)-valencene by recombinant E. coli expressing CYP109B1 from Bacillus subtilis in a two-liquid-phase system.
2009 Jul 10
Hepatoprotective activity of petroleum ether, diethyl ether, and methanol extract of Scoparia dulcis L. against CCl4-induced acute liver injury in mice.
2009 Jun
Biology by design: from top to bottom and back.
2010
Identification of a GCC transcription factor responding to fruit colour change events in citrus through the transcriptomic analyses of two mutants.
2010 Dec 15
A dioxygenase of Pleurotus sapidus transforms (+)-valencene regio-specifically to (+)-nootkatone via a stereo-specific allylic hydroperoxidation.
2010 Jan
Catalytic oxidation of concentrated orange oil phase by synthetic metallic complexes biomimetic to MMO enzyme.
2010 Jul
Variation of herbivore-induced volatile terpenes among Arabidopsis ecotypes depends on allelic differences and subcellular targeting of two terpene synthases, TPS02 and TPS03.
2010 Jul
Name Type Language
VALENCENE
FHFI   INCI  
INCI  
Official Name English
VALENCENE [INCI]
Common Name English
4.BETA.H,5.ALPHA.-EREMOPHILA-1(10),11-DIENE
Common Name English
NAPHTHALENE, 1,2,3,5,6,7,8,8A-OCTAHYDRO-1,8A-DIMETHYL-7-(1-METHYLETHENYL)-, (1R-(1.ALPHA.,7.BETA.,8A.ALPHA.))-
Common Name English
VALENCEN
Common Name English
NSC-148969
Code English
(+)-VALENCENE
Common Name English
VALENCENE [FHFI]
Common Name English
FEMA NO. 3443
Code English
NAPHTHALENE, 1,2,3,5,6,7,8,8A-OCTAHYDRO-1,8A-DIMETHYL-7-(1-METHYLETHENYL)-, (1R,7R,8AS)-
Common Name English
Classification Tree Code System Code
JECFA EVALUATION VALENCENE
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
Code System Code Type Description
NSC
148969
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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CAS
4630-07-3
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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FDA UNII
96H21P91IG
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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EPA CompTox
DTXSID8047052
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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CHEBI
61700
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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EVMPD
SUB179380
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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SMS_ID
100000164813
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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DAILYMED
96H21P91IG
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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WIKIPEDIA
VALENCENE
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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ECHA (EC/EINECS)
225-047-6
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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PUBCHEM
9855795
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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MESH
C506706
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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JECFA MONOGRAPH
1336
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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RXCUI
2569979
Created by admin on Fri Dec 15 19:48:49 GMT 2023 , Edited by admin on Fri Dec 15 19:48:49 GMT 2023
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