Oksmetidin
(IUPAC) ime | |||
---|---|---|---|
5-(1,3-benzodioksol-5-ilmetil)-2-[(2[(5-metil-1H-imidazol-4-il)metil]sulfanil}etil)amino]pirimidin-4(3H)-on | |||
Klinički podaci | |||
Identifikatori | |||
CAS broj | 72830-39-8 | ||
ATC kod | nije dodeljen | ||
PubChem[1][2] | 51710 | ||
ChemSpider[3] | 46799 | ||
UNII | Z504D030RF Y | ||
Hemijski podaci | |||
Formula | C19H21N5O3S | ||
Mol. masa | 399,47 g/mol | ||
SMILES | eMolekuli & PubHem | ||
| |||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Oksmetidin je antagonist H2 receptora.[4]
Reference
- ↑ 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
- ↑ 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. edit
- ↑ Willson, R. A.; Hall, T; Hart, J. (1987-10-24). „Oxmetidine (H2 receptor antagonist) induced cytotoxicity in isolated rat hepatocytes”. Journal of Applied Toxicology 8 (3): 223–225. DOI:10.1002/jat.2550080311. PMID 2902116.
Spoljašnje veze
Portal Medicina | |
Portal Hemija |
- p
- r
- u
Inhibitori: Aminoguanidin |
Histamin; Prekursori: L-Histidin; Kofaktori: Vitamin B6 |