Sulproston
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(IUPAC) ime | |||
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(Z)-7-[(1R,3R)-3-Hidroksi-2-[(E,3R)-3-hidroksi-4-fenoksibut-1-enil]-5-oksociklopentil]-N-metilsulfonilhept-5-enamid | |||
Klinički podaci | |||
AHFS/Drugs.com | Internacionalno ime leka | ||
Identifikatori | |||
CAS broj | 60325-46-4 | ||
ATC kod | G02AD05 | ||
PubChem[1][2] | 6917982 | ||
UNII | 501Q5EQ1GM ![]() | ||
KEGG[3] | D02725 ![]() | ||
ChEMBL[4] | CHEMBL284178 ![]() | ||
Hemijski podaci | |||
Formula | C23H31NO7S | ||
Mol. masa | 465,56 g/mol | ||
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Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status |
Sulproston je uterotonik.
On je analog prostaglandina E2.[5]
- ↑ 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.
- ↑ 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.
- ↑ 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 21948863.
- ↑ Tamma G, Wiesner B, Furkert J, et al. (August 2003). „The prostaglandin E2 analogue sulprostone antagonizes vasopressin-induced antidiuresis through activation of Rho”. Journal of Cell Science 116 (Pt 16): 3285–94. DOI:10.1242/jcs.00640. PMID 12829746.