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O-823

Izvor: Wikipedija
O-823
(IUPAC) ime
7-[(6aR,10aR)-1-hidroksi-6,6,9-trimetil-6a,7,10,10a-tetrahidrobenzo[c]hromen-3-il]hept-5-inenitril
Klinički podaci
Identifikatori
ATC kod nije dodeljen
PubChem[1][2] 9863194
ChemSpider[3] 8038890
Hemijski podaci
Formula C23H27NO2 
Mol. masa 349,465 g/mol
SMILES eMolekuli & PubHem
Farmakoinformacioni podaci
Trudnoća ?
Pravni status

O-823 je lek koji je kanabinoidni derivat sa primenom u naučnim istraživanjima. On je mešoviti agonist/antagonist kanabinoidnog receptora CB1. Drugim rečima on deluje kao antagonist kad se dozira zajedno sa potentnijim CB1 agonistom, dok je slab parcijalni agonist u odsustvu drugog agonist.[4][5][6]

Reference

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  1. Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519.  edit
  2. Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1. 
  3. Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846.  edit
  4. Pertwee RG, Fernando SR, Griffin G, Ryan W, Razdan RK, Compton DR, Martin BR. Agonist-antagonist characterization of 6'-cyanohex-2'-yne-delta 8-tetrahydrocannabinol in two isolated tissue preparations. European Journal of Pharmacology. 1996 Nov 14;315(2):195-201. PMID 8960884
  5. Griffin G, Wray EJ, Rorrer WK, Crocker PJ, Ryan WJ, Saha B, Razdan RK, Martin BR, Abood ME. An investigation into the structural determinants of cannabinoid receptor ligand efficacy. British Journal of Pharmacology. 1999 Apr;126(7):1575-84. DOI:10.1038/sj.bjp.0702469 PMID 10323589
  6. Griffin G, Wray EJ, Martin BR, Abood ME. Cannabinoid agonists and antagonists discriminated by receptor binding in rat cerebellum. British Journal of Pharmacology. 1999 Oct;128(3):684-8. DOI:10.1038/sj.bjp.0702806 PMID 10516649

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