A-366,833
(Preusmjereno sa stranice GPXAWLDGWSBLKM-ONGXEEELSA-N)
A-366,833 je lek koji je razvilo preduzeće Abbott. On deluje kao agonist na neuronskom nikotinskim acetilholinskim receptorima. Selektivan je za α4β2 podtip, i izučavan je za moguću primenu kao analgetik, mada nije uspešno prošao kroz klinička ispitivanja.[5][6]
(IUPAC) ime | |||
---|---|---|---|
5-[(1S,5R)-3,6-diazabiciklo[3.2.0]hept-6-il]piridin-3-karbonitril | |||
Klinički podaci | |||
Identifikatori | |||
ATC kod | nije dodeljen | ||
PubChem[1][2] | 9834234 | ||
ChemSpider[3] | 8009955 | ||
ChEMBL[4] | CHEMBL239931 | ||
Hemijski podaci | |||
Formula | C11H12N4 | ||
Mol. masa | 200,239 | ||
| |||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Reference uredi
- ↑ 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.
- ↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594.
- ↑ Ji, J.; Bunnelle, W.; Anderson, D.; Faltynek, C.; Dyhring, T.; Ahring, P.; Rueter, L.; Curzon, P. i dr.. (2007). „A-366833: a novel nicotinonitrile-substituted 3,6-diazabicyclo3.2.0-heptane alpha4beta2 nicotinic acetylcholine receptor selective agonist: Synthesis, analgesic efficacy and tolerability profile in animal models”. Biochemical pharmacology 74 (8): 1253–1262. DOI:10.1016/j.bcp.2007.08.010. PMID 17854775.
- ↑ Romanelli, M.; Gratteri, P.; Guandalini, L.; Martini, E.; Bonaccini, C.; Gualtieri, F. (2007). „Central nicotinic receptors: structure, function, ligands, and therapeutic potential”. ChemMedChem 2 (6): 746–767. DOI:10.1002/cmdc.200600207. PMID 17295372.