Alazocin
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(IUPAC) ime | |||
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(2R,6R,11R)- 6,11-dimethyl- 3-prop- 2-en- 1-yl- 1,2,3,4,5,6-hexahydro- 2,6-methano- 3-benzazocin- 8-ol 2-allyl- 5,9-dimethyl- 2'-hydroxy- 6,7-benzomorphan | |||
Klinički podaci | |||
Identifikatori | |||
CAS broj | 14198-28-8 | ||
ATC kod | nije dodeljen | ||
PubChem[1][2] | 3036246 | ||
ChemSpider[3] | 2300306 | ||
Hemijski podaci | |||
Formula | C17H23NO | ||
Mol. masa | 257.37 g/mol | ||
SMILES | eMolekuli & PubHem | ||
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Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status | Uncontrolled | ||
Način primene | ? |
Alazocin ((-)-SKF-10,047, (-)-N-alilnormetazocin, (-)-ANMC), je bio prvi lek koji je agonist σ1 receptora (Ki = 24 nM).[4][5][6] On nema značajan afinitet za σ2 receptor.[6] Alazocin takođe deluje kao agonist κ-opioidnog receptora (Ki = 0.4 nM), i u znatno manjoj meri kao antagonist NMDA receptora (Ki = 587 nM).[6][7]
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ Iwamoto ET (February 1981). „Pharmacologic effects of N-allylnormetazocine (SKF-10047)”. NIDA research monograph 34: 82–8. PMID 6783955.
- ↑ Shearman GT, Herz A (August 1982). „Non-opioid psychotomimetic-like discriminative stimulus properties of N-allylnormetazocine (SKF 10,047) in the rat”. European journal of pharmacology 82 (3-4): 167–72. PMID 6290235.
- ↑ 6,0 6,1 6,2 Chou YC, Liao JF, Chang WY, Lin MF, Chen CF (March 1999). „Binding of dimemorfan to sigma-1 receptor and its anticonvulsant and locomotor effects in mice, compared with dextromethorphan and dextrorphan”. Brain Research 821 (2): 516–9. DOI:10.1016/S0006-8993(99)01125-7. PMID 10064839.
- ↑ Gharagozlou P, Hashemi E, DeLorey TM, Clark JD, Lameh J (2006). „Pharmacological profiles of opioid ligands at kappa opioid receptors”. BMC Pharmacology 6: 3. DOI:10.1186/1471-2210-6-3. PMC 1403760. PMID 16433932.