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Olivetol

CAS No.:
500-66-3
Catalog Number:
AG0035FJ
Molecular Formula:
C11H16O2
Molecular Weight:
180.2435
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$38
- +
5g
98%
In Stock USA
United States
$81
- +
10g
98%
In Stock USA
United States
$125
- +
25g
98%
In Stock USA
United States
$250
- +
100g
98%
In Stock USA
United States
$625
- +
Product Description
Catalog Number:
AG0035FJ
Chemical Name:
Olivetol
CAS Number:
500-66-3
Molecular Formula:
C11H16O2
Molecular Weight:
180.2435
MDL Number:
MFCD00002293
IUPAC Name:
5-pentylbenzene-1,3-diol
InChI:
InChI=1S/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3
InChI Key:
IRMPFYJSHJGOPE-UHFFFAOYSA-N
SMILES:
CCCCCc1cc(O)cc(c1)O
EC Number:
207-908-8
UNII:
65OP0NEZ1P
Properties
Complexity:
126  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
180.115g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
180.247g/mol
Monoisotopic Mass:
180.115g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
40.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.6  
Literature
Title Journal
Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol. Chemico-biological interactions 20140525
Cannabidiol, a major phytocannabinoid, as a potent atypical inhibitor for CYP2D6. Drug metabolism and disposition: the biological fate of chemicals 20111101
Potent inhibition of human cytochrome P450 3A isoforms by cannabidiol: role of phenolic hydroxyl groups in the resorcinol moiety. Life sciences 20110411
Comparative genomics of the social amoebae Dictyostelium discoideum and Dictyostelium purpureum. Genome biology 20110101
Phase I hydroxylated metabolites of the K2 synthetic cannabinoid JWH-018 retain in vitro and in vivo cannabinoid 1 receptor affinity and activity. PloS one 20110101
Antioxidant, antimicrobial and antiproliferative activities of five lichen species. International journal of molecular sciences 20110101
Systematic review of herbals as potential anti-inflammatory agents: Recent advances, current clinical status and future perspectives. Pharmacognosy reviews 20110101
Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products. The Journal of biological chemistry 20101217
Alkylresorcinol synthases expressed in Sorghum bicolor root hairs play an essential role in the biosynthesis of the allelopathic benzoquinone sorgoleone. The Plant cell 20100301
In silicio expression analysis of PKS genes isolated from Cannabis sativa L. Genetics and molecular biology 20100101
Identification of candidate genes affecting Delta9-tetrahydrocannabinol biosynthesis in Cannabis sativa. Journal of experimental botany 20090901
Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway. FEBS letters 20090618
HTRF: A technology tailored for drug discovery - a review of theoretical aspects and recent applications. Current chemical genomics 20090101
Chemoenzymatic syntheses of prenylated aromatic small molecules using Streptomyces prenyltransferases with relaxed substrate specificities. Bioorganic & medicinal chemistry 20080901
Antibacterial cannabinoids from Cannabis sativa: a structure-activity study. Journal of natural products 20080801
Activities of 2,4-dihydroxy-6-n-pentylbenzoic acid derivatives. Zeitschrift fur Naturforschung. C, Journal of biosciences 20080101
Design, synthesis, binding, and molecular modeling studies of new potent ligands of cannabinoid receptors. Bioorganic & medicinal chemistry 20070815
Biosynthesis of lipid resorcinols and benzoquinones in isolated secretory plant root hairs. Journal of experimental botany 20070101
In vitro and in vivo pharmacology of synthetic olivetol- or resorcinol-derived cannabinoid receptor ligands. British journal of pharmacology 20061001
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. Nature 20050616
Cloning and over-expression of a cDNA encoding a polyketide synthase from Cannabis sativa. Plant physiology and biochemistry : PPB 20040401
Prenylation of olivetolate by a hemp transferase yields cannabigerolic acid, the precursor of tetrahydrocannabinol. FEBS letters 19980508
Properties