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Details

Stereochemistry ABSOLUTE
Molecular Formula C10H14O
Molecular Weight 150.2176
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARVONE, (+)-

SMILES

CC(=C)[C@H]1CC=C(C)C(=O)C1

InChI

InChIKey=ULDHMXUKGWMISQ-VIFPVBQESA-N
InChI=1S/C10H14O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9H,1,5-6H2,2-3H3/t9-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H14O
Molecular Weight 150.2176
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
A mass transport model of olfaction.
1994 Mar 21
Enantioselective syntheses of authentic sclerophytin A, sclerophytin B, and cladiell-11-ene-3,6,7-triol.
2001 Jan 11
Mechanism of the antigen formation of carvone and related alpha, beta-unsaturated ketones.
2001 Jun
Effects of chiral fragrances on human autonomic nervous system parameters and self-evaluation.
2001 Mar
Percutaneous absorption of the montoterperne carvone: implication of stereoselective metabolism on blood levels.
2001 May
A general strategy for the synthesis of cladiellin diterpenes: enantioselective total syntheses of 6-acetoxycladiell-7(16),11-dien-3-ol (deacetoxyalcyonin acetate), cladiell-11-ene-3,6,7-triol, sclerophytin A, and the initially purported structure of sclerophytin A.
2001 Sep 19
Efficient synthesis of 1alpha-fluoro A-ring phosphine oxide, a useful building block for vitamin D analogues, from (S)-carvone via a highly selective palladium-catalyzed isomerization of dieneoxide to dieneol.
2001 Sep 7
Species differences in the metabolism of (+)- and (-)-limonenes and their metabolites, carveols and carvones, by cytochrome P450 enzymes in liver microsomes of mice, rats, guinea pigs, rabbits, dogs, monkeys, and humans.
2002
Efficient synthesis of the A-ring phosphine oxide building block useful for 1 alpha,25-dihydroxy vitamin D(3) and analogues.
2002 Mar 8
Two in vitro models for gas-phase exposure to volatile compounds.
2002 Mar-Apr
Detection and discrimination of carvone enantiomers in rats with olfactory bulb lesions.
2003
A route to the thapsigargins from (S)-carvone providing a substrate-controlled total synthesis of trilobolide, nortrilobolide, and thapsivillosin F.
2003 Dec 15
Efficient synthesis of novel 1alpha-amino and 3beta-amino analogues of 1alpha,25-dihydroxyvitamin d(3).
2003 Feb 7
Concanavalin A application to the olfactory epithelium reveals different sensory neuron populations for the odour pair D- and L-carvone.
2003 Jan 22
Changes of the volatile profile and artifact formation in Daidai (Citrus aurantium) cold-pressed peel oil on storage.
2003 Jul 2
Composition, quality control, and antimicrobial activity of the essential oil of long-time stored dill (Anethum graveolens L.) seeds from Bulgaria.
2003 Jun 18
Enantioselective total synthesis of briarellins E and F: the first total syntheses of briarellin diterpenes.
2003 Jun 4
Bioactivities of l-carvone, d-carvone, and dihydrocarvone toward three stored product beetles.
2003 Oct
Toxicological efficacy of some indigenous dill compounds against the flesh fly, Parasarcophaga dux Thomson.
2004 Apr
The effect of selected monoterpenoids on the cellular slime mold, Dictyostelium discoideum NC4.
2004 Jun
Diastereoselective reactions at enantiomerically pure, sterically congested cyclohexanes as an entry to wailupemycins A and B: total synthesis of (+)-wailupemycin B.
2005 Nov 18
Vapor phase toxicity of marjoram oil compounds and their related monoterpenoids to Blattella germanica (Orthoptera: Blattellidae).
2005 Oct 5
Versatile synthesis and biological evaluation of 1,3-diamino-substituted 1alpha,25-dihydroxyvitamin D3 analogues.
2006 Feb 15
Antinociceptive activity of structural analogues of rotundifolone: structure-activity relationship.
2007 Jan-Feb
Toward the synthesis of norzoanthamine: complete fragment assembly.
2007 Jun 22
Influence of the chirality of (R)-(-)- and (S)-(+)-carvone in the central nervous system: a comparative study.
2007 May 5
Influence of different extraction parameters on a solid-phase dynamic extraction for the gas chromatographic determination of d-limonene degradation products by using a fractional factorial design.
2007 Nov-Dec
Response accuracy and odor sampling time in mice trained to discriminate between enantiomers of carvone and those of terpinen-4-ol.
2007 Sep
Structure and spasmolytic activity relationships of monoterpene analogues found in many aromatic plants.
2008 Nov-Dec
Use of human senses as sensors.
2009
Molecular sensing by nanoporous crystalline polymers.
2009
Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants.
2009 Mar 11
Enantiospecific synthesis of the cubitane skeleton.
2010 Feb 19
Anethum graveolens: An Indian traditional medicinal herb and spice.
2010 Jul
Distinct effects of carvone analogues on the isolated nerve of rats.
2010 Oct 25
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:01:07 GMT 2023
Edited
by admin
on Sat Dec 16 05:01:07 GMT 2023
Record UNII
4RWC1CMS3X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARVONE, (+)-
Common Name English
2-CYCLOHEXEN-1-ONE, 2-METHYL-5-(1-METHYLETHENYL)-, (5S)-
Systematic Name English
CARVONE D-FORM [MI]
Common Name English
(S)-(+)-P-MENTHA-6,8-DIEN-2-ONE
Common Name English
CARVONE D-
Common Name English
S-(+)-CARVONE
Common Name English
2-CYCLOHEXEN-1-ONE, 2-METHYL-5-(1-METHYLETHENYL)-, (S)-
Systematic Name English
(S)-D-P-MENTHA-6,8,(9)-DIEN-2-ONE
Common Name English
D-CARVONE
Common Name English
FEMA NO. 2249, (+)-
Code English
(S)-(+)-CARVONE
Common Name English
(+)-CARVONE [FCC]
Common Name English
(+)-CARVONE
FCC  
Common Name English
P-MENTHA-6,8-DIEN-2-ONE, (S)-(+)-
Common Name English
CARVONE, D-
Common Name English
(S)-CARVONE
Common Name English
(S)-2-METHYL-5-(1-METHYLVINYL)CYCLOHEX-2-EN-1-ONE
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION (+)-CARVONE
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
Code System Code Type Description
PUBCHEM
16724
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
JECFA MONOGRAPH
348
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
FDA UNII
4RWC1CMS3X
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID8020256
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
CHEBI
15399
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
RXCUI
1747726
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-827-2
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
MERCK INDEX
m3144
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY Merck Index
CAS
2244-16-8
Created by admin on Sat Dec 16 05:01:07 GMT 2023 , Edited by admin on Sat Dec 16 05:01:07 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
ASSAY (GC)