Lupitidin
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(IUPAC) ime | |||
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2-({2-[({5-[(dimetilamino)metil]furan-2-il}metil)sulfanil]etil}amino)-5-[(6-metilpiridin-3-il)metil]pirimidin-4(3H)-on | |||
Klinički podaci | |||
Identifikatori | |||
CAS broj | 83903-06-4 | ||
ATC kod | nije dodeljen | ||
PubChem[1][2] | 51670 | ||
ChemSpider[3] | 3577726 | ||
UNII | WF028DWK9N ![]() | ||
KEGG[4] | D04794 | ||
Hemijski podaci | |||
Formula | C21H27N5O2S | ||
Mol. masa | 413,54 g/mol | ||
SMILES | eMolekuli & PubHem | ||
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Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Lupitidin je antagonist H2 receptora. On deluje kao agens protiv čireva.
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
- ↑ Joanne Wixon, Douglas Kell (2000). „Website Review: The Kyoto Encyclopedia of Genes and Genomes — KEGG”. Yeast 17 (1): 48–55. DOI:10.1002/(SICI)1097-0061(200004)17:1<48::AID-YEA2>3.0.CO;2-H.
Literatura
- Lam, B. L.; Pridgen, L. N.; 1982, U.S. Patent 4,352,933.
Spoljašnje veze
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Inhibitori: Aminoguanidin |
Histamin; Prekursori: L-Histidin; Kofaktori: Vitamin B6 |