Parikalcitol
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(IUPAC) ime
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(1R,3R,7E,17β)-17-[(1R,2E,4S)-5-hidroksi-1,4,5-trimetilheks-2-en-1-il]-9,10-sekoestra-5,7-dien-1,3-diol
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Klinički podaci
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AHFS/Drugs.com
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Monografija
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MedlinePlus
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a682335
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Identifikatori
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CAS broj
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131918-61-1
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ATC kod
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H05BX02
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PubChem[1][2]
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5281104
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DrugBank
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DB00910
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ChemSpider[3]
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4444552
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UNII
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6702D36OG5 Y
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KEGG[4]
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D00930 Y
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ChEBI
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CHEBI:7931 Y
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ChEMBL[5]
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CHEMBL1200622 Y
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Hemijski podaci
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Formula
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C27H44O3
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Mol. masa
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416,636 g/mol
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InChI |
InChI=1S/C27H44O3/c1-18(8-9-19(2)26(3,4)30)24-12-13-25-21(7-6-14-27(24,25)5)11-10-20-15-22(28)17-23(29)16-20/h8-11,18-19,22-25,28-30H,6-7,12-17H2,1-5H3/b9-8+,21-11+/t18-,19+,22-,23-,24-,25+,27-/m1/s1 Y Key: BPKAHTKRCLCHEA-UBFJEZKGSA-N Y |
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Sinonimi
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(1R,3S)-5-[2-[(1R,3aR,7aS)-1-[(2R,5S)-6-hidroksi-5,6-dimetil-3E-hepten-2-il]-7a-metil-2,3,3a,5,6,7-heksahidro-1H-inden-4-iliden]etiliden]-ciklohexan-1,3-diol
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Farmakokinetički podaci
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Bioraspoloživost
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N/A
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Poluvreme eliminacije
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5 do 7 sati
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Izlučivanje
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Biliary
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Farmakoinformacioni podaci
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Trudnoća
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?
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Pravni status
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Način primene
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Oralno, intravenozno
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Parikalcitol (Zemplar) je lek koji se koristi za sprećavanje i tretman sekundarnog hiperparatiroidizma (ekscesivne sekrecije paratiroidnog hormona) vezanog za hroničnu bubrežnu insuficijenciju. Hemijski, on je 19-nor-1,25-(OH)2-vitamin D2 ili 19-nor-1,25-dihidroksivitamin D2. On je analog 1,25-dihidroksiergokalciferola, aktivne forme vitamina D2.[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. 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.
- ↑ 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. edit
- ↑ Hardman JG, Limbird LE, Gilman AG. (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10 izd.). New York: McGraw-Hill. DOI:10.1036/0071422803. ISBN 0-07-135469-7.
- ↑ Pdr Staff (2009). PDR: Physicians Desk Reference 2010 (Physicians' Desk Reference (Pdr)). Rozelle, N.S.W: Thomson Reuters. ISBN 1-56363-748-0.