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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

Molecular Formula C15H24
Molecular Weight 204.3511
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Identification of a GCC transcription factor responding to fruit colour change events in citrus through the transcriptomic analyses of two mutants.
2010-12-15
Catalytic oxidation of concentrated orange oil phase by synthetic metallic complexes biomimetic to MMO enzyme.
2010-07
Variation of herbivore-induced volatile terpenes among Arabidopsis ecotypes depends on allelic differences and subcellular targeting of two terpene synthases, TPS02 and TPS03.
2010-07
A dioxygenase of Pleurotus sapidus transforms (+)-valencene regio-specifically to (+)-nootkatone via a stereo-specific allylic hydroperoxidation.
2010-01
Biology by design: from top to bottom and back.
2010
Essential oils from two Lantana species with antimycobacterial activity.
2009-12
Regioselective biooxidation of (+)-valencene by recombinant E. coli expressing CYP109B1 from Bacillus subtilis in a two-liquid-phase system.
2009-07-10
Hepatoprotective activity of petroleum ether, diethyl ether, and methanol extract of Scoparia dulcis L. against CCl4-induced acute liver injury in mice.
2009-06
Nootkatone--a biotechnological challenge.
2009-05
Rational design of a minimal and highly enriched CYP102A1 mutant library with improved regio-, stereo- and chemoselectivity.
2009-03-23
Montanoa tomentosa glandular trichomes containing kaurenoic acids chemical profile and distribution.
2009-01
[Characterization of aroma active compounds in blood orange juice by solid phase microextraction and gas chromatography-mass spectrometry-olfactometry].
2008-07
Production of plant sesquiterpenes in Saccharomyces cerevisiae: effect of ERG9 repression on sesquiterpene biosynthesis.
2008-02-15
Herbivore-induced terpenoid emission in Medicago truncatula: concerted action of jasmonate, ethylene and calcium signaling.
2008-01
Citrus genomics.
2008
[Increase of copy number of HMG-CoA reductase and FPP synthase genes improves the amorpha4,11-diene production in engineered yeast].
2007-12
Essential Oil Composition and Antibacterial Studies of Vitex negundo Linn. Extracts.
2007-05-28
[GC-MS analysis of volatile constituents from five different kinds of Chinese eaglewood].
2007-05
Chemical composition of the essential oil of Pelargonium quercetorum Agnew. of Iran.
2007-01
Valence isomerization of 2-phospha-4-silabicyclo[1.1.0]butane: a high-level ab initio study.
2006-07
Analysis of the essential oil composition from the different parts of Eryngiumglaciale Boiss. from Spain.
2005-11-11
Highly efficient production of nootkatone, the grapefruit aroma from valencene, by biotransformation.
2005-11
Biotransformation of citrus aromatics nootkatone and valencene by microorganisms.
2005-11
Headspace solid-phase microextraction-gas chromatography--mass spectrometry analysis of the volatile compounds of Evodia species fruits.
2005-09-16
Use of novel compounds for pest control: insecticidal and acaricidal activity of essential oil components from heartwood of Alaska yellow cedar.
2005-05
Biotransformation of the sesquiterpene (+)-valencene by cytochrome P450cam and P450BM-3.
2005-01-07
[Chemical components of Vetiveria zizanioides volatiles].
2004-01
Structure-activity of valencenoid derivatives and their repellence to the Formosan subterranean termite.
2003-12
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.
2003-12
Identification of aroma active compounds in orange essence oil using gas chromatography-olfactometry and gas chromatography-mass spectrometry.
2003-05-23
The sesquiterpenoid nootkatone and the absolute configuration of a dibromo derivative.
2003-05
Volatiles from leaves, fruits, and virgin oil from Olea europaea Cv. Olivastra Seggianese from Italy.
2003-02-26
Monitoring and fast detection of mycotoxin-producing fungi based on headspace solid-phase microextraction and headspace sorptive extraction of the volatile metabolites.
2003-01-24
Influence of flavour absorption by food-packaging materials (low-density polyethylene, polycarbonate and polyethylene terephthalate) on taste perception of a model solution and orange juice.
2003-01
Volatile sesquiterpene hydrocarbons characteristic for Penicillium roqueforti strains producing PR toxin.
2002-10-23
Germacrene A is a product of the aristolochene synthase-mediated conversion of farnesylpyrophosphate to aristolochene.
2002-10-02
Effects of pulsed electric field processing and storage on the quality and stability of single-strength orange juice.
2002-10
Volatile chemicals identified in extracts from newly hybrid citrus, dekopon (Shiranuhi mandarin Suppl. J.).
2002-09-11
[Chemical constituents in volatile oil from fruits of Alpinia oxyphylla Miq].
2001-04
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:57:49 GMT 2025
Edited
by admin
on Mon Mar 31 19:57:49 GMT 2025
Record UNII
96H21P91IG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VALENCENE
FHFI   INCI  
INCI  
Official Name English
FEMA NO. 3443
Preferred 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
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 Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
Code System Code Type Description
NSC
148969
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
CAS
4630-07-3
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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FDA UNII
96H21P91IG
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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EPA CompTox
DTXSID8047052
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
CHEBI
61700
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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EVMPD
SUB179380
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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SMS_ID
100000164813
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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DAILYMED
96H21P91IG
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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WIKIPEDIA
VALENCENE
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
ECHA (EC/EINECS)
225-047-6
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
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PUBCHEM
9855795
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
MESH
C506706
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
JECFA MONOGRAPH
1336
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY
RXCUI
2569979
Created by admin on Mon Mar 31 19:57:49 GMT 2025 , Edited by admin on Mon Mar 31 19:57:49 GMT 2025
PRIMARY