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
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
| 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
| Title | Date | PubMed |
|---|---|---|
| Characterization of the structural determinants required for potent mechanism-based inhibition of human cytochrome P450 1A1 by cannabidiol. | 2014-05-25 |
|
| Functional characterization of the promiscuous prenyltransferase responsible for furaquinocin biosynthesis: identification of a physiological polyketide substrate and its prenylated reaction products. | 2010-12-17 |
|
| In silicio expression analysis of PKS genes isolated from Cannabis sativa L. | 2010-10 |
|
| Alkylresorcinol synthases expressed in Sorghum bicolor root hairs play an essential role in the biosynthesis of the allelopathic benzoquinone sorgoleone. | 2010-03 |
|
| Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway. | 2009-06-18 |
|
| HTRF: A technology tailored for drug discovery - a review of theoretical aspects and recent applications. | 2009-05-28 |
|
| Identification of candidate genes affecting Delta9-tetrahydrocannabinol biosynthesis in Cannabis sativa. | 2009 |
|
| Antibacterial cannabinoids from Cannabis sativa: a structure-activity study. | 2008-08 |
|
| Activities of 2,4-dihydroxy-6-n-pentylbenzoic acid derivatives. | 2008-04-05 |
|
| Design, synthesis, binding, and molecular modeling studies of new potent ligands of cannabinoid receptors. | 2007-08-15 |
|
| Biosynthesis of lipid resorcinols and benzoquinones in isolated secretory plant root hairs. | 2007 |
|
| In vitro and in vivo pharmacology of synthetic olivetol- or resorcinol-derived cannabinoid receptor ligands. | 2006-10 |
|
| Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products. | 2005-06-16 |
|
| Cloning and over-expression of a cDNA encoding a polyketide synthase from Cannabis sativa. | 2004-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:22:44 GMT 2025
by
admin
on
Mon Mar 31 19:22:44 GMT 2025
|
| Record UNII |
65OP0NEZ1P
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C016630
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
DTXSID0025812
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
207-908-8
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
500-66-3
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
10377
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
65OP0NEZ1P
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
66960
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY | |||
|
OLIVETOL
Created by
admin on Mon Mar 31 19:22:44 GMT 2025 , Edited by admin on Mon Mar 31 19:22:44 GMT 2025
|
PRIMARY |