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Details

Stereochemistry ACHIRAL
Molecular Formula C11H16O2
Molecular Weight 180.2435
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OLIVETOL

SMILES

CCCCCC1=CC(O)=CC(O)=C1

InChI

InChIKey=IRMPFYJSHJGOPE-UHFFFAOYSA-N
InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3

HIDE SMILES / InChI

Molecular Formula C11H16O2
Molecular Weight 180.2435
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Cloning and over-expression of a cDNA encoding a polyketide synthase from Cannabis sativa.
2004 Apr
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products.
2005 Jun 16
In vitro and in vivo pharmacology of synthetic olivetol- or resorcinol-derived cannabinoid receptor ligands.
2006 Oct
Biosynthesis of lipid resorcinols and benzoquinones in isolated secretory plant root hairs.
2007
Design, synthesis, binding, and molecular modeling studies of new potent ligands of cannabinoid receptors.
2007 Aug 15
Antibacterial cannabinoids from Cannabis sativa: a structure-activity study.
2008 Aug
Activities of 2,4-dihydroxy-6-n-pentylbenzoic acid derivatives.
2008 Jan-Feb
Identification of candidate genes affecting Delta9-tetrahydrocannabinol biosynthesis in Cannabis sativa.
2009
Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway.
2009 Jun 18
HTRF: A technology tailored for drug discovery - a review of theoretical aspects and recent applications.
2009 May 28
Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products.
2010 Dec 17
Alkylresorcinol synthases expressed in Sorghum bicolor root hairs play an essential role in the biosynthesis of the allelopathic benzoquinone sorgoleone.
2010 Mar
In silicio expression analysis of PKS genes isolated from Cannabis sativa L.
2010 Oct
Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol.
2014 May 25
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:51:19 GMT 2023
Edited
by admin
on Fri Dec 15 18:51:19 GMT 2023
Record UNII
65OP0NEZ1P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OLIVETOL
Systematic Name English
5-PENTYL-1,3-BENZENEDIOL
Systematic Name English
5-PENTYLRESORCINOL
Systematic Name English
1,3-BENZENEDIOL, 5-PENTYL-
Systematic Name English
3,5-DIHYDROXYAMYLBENZENE
Systematic Name English
Code System Code Type Description
MESH
C016630
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID0025812
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-908-8
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY
CAS
500-66-3
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
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PUBCHEM
10377
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
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FDA UNII
65OP0NEZ1P
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
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CHEBI
66960
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
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WIKIPEDIA
OLIVETOL
Created by admin on Fri Dec 15 18:51:19 GMT 2023 , Edited by admin on Fri Dec 15 18:51:19 GMT 2023
PRIMARY