Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H20 |
| Molecular Weight | 128.2551 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCC(C)C
InChI
InChIKey=ZUBZATZOEPUUQF-UHFFFAOYSA-N
InChI=1S/C9H20/c1-4-5-6-7-8-9(2)3/h9H,4-8H2,1-3H3
| Molecular Formula | C9H20 |
| Molecular Weight | 128.2551 |
| 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 |
|---|---|---|
| Association of exposure to phthalates with endometriosis and uterine leiomyomata: findings from NHANES, 1999-2004. | 2010-06 |
|
| The intrasectional chemotaxonomic placement of Hypericum elegans Stephan ex Willd. Inferred from the essential-oil chemical composition. | 2010-04 |
|
| New resorcinol-anandamide "hybrids" as potent cannabinoid receptor ligands endowed with antinociceptive activity in vivo. | 2009-04-23 |
|
| Biodegradation of mono-alkyl phthalate esters in natural sediments. | 2008-05 |
|
| Binding mode prediction of conformationally restricted anandamide analogs within the CB1 receptor. | 2008-02-26 |
|
| Cannabinoids in the management of difficult to treat pain. | 2008-02 |
|
| Sex pheromone of Elater ferrugineus L. (Coleoptera: Elateridae). | 2007-11 |
|
| Synthesis and CB1 receptor activities of dimethylheptyl derivatives of 2-arachidonoyl glycerol (2-AG) and 2-arachidonyl glyceryl ether (2-AGE). | 2006-04-15 |
|
| Harm reduction--the cannabis paradox. | 2005-09-22 |
|
| Enantiomeric cannabidiol derivatives: synthesis and binding to cannabinoid receptors. | 2005-03-21 |
|
| Ecotoxicity and biodegradation of phthalate monoesters. | 2003-12 |
|
| First tests of a liquid ionization chamber to monitor intensity modulated radiation beams. | 2003-11-07 |
|
| Cannabinoid agonists and antagonists modulate lithium-induced conditioned gaping in rats. | 2003-10-07 |
|
| The CB1 cannabinoid receptor agonist, HU-210, reduces levodopa-induced rotations in 6-hydroxydopamine-lesioned rats. | 2003-08 |
|
| 1-Methoxy-, 1-deoxy-11-hydroxy- and 11-hydroxy-1-methoxy-Delta(8)-tetrahydrocannabinols: new selective ligands for the CB2 receptor. | 2002-12 |
|
| Cannabidiol, a non-psychoactive component of cannabis and its synthetic dimethylheptyl homolog suppress nausea in an experimental model with rats. | 2002-04-16 |
|
| Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide. | 2001-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:40:53 GMT 2025
by
admin
on
Mon Mar 31 18:40:53 GMT 2025
|
| Record UNII |
AV5KXW7I9L
|
| Record Status |
Validated (UNII)
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| Record Version |
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23695
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3221-61-2
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221-748-6
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2-Methyloctane
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DTXSID30863125
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18591
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