Pindolol
Pindolol (Visken, Betapindol, Blockin L, Blocklin L, Calvisken, Cardilate, Decreten, Durapindol, Glauco-Visken, Pectobloc, Pinbetol, Prindolol, Pynastin) je beta blokator.[6][7]
(IUPAC) ime | |||
---|---|---|---|
(RS)-1-(1H-indol-4-iloksi)-3-(izopropilamino)propan-2-ol | |||
Klinički podaci | |||
AHFS/Drugs.com | Monografija | ||
MedlinePlus | a684032 | ||
Identifikatori | |||
CAS broj | 13523-86-9 | ||
ATC kod | C07AA03 | ||
PubChem[1][2] | 4828 | ||
DrugBank | DB00960 | ||
ChemSpider[3] | 4662 | ||
UNII | BJ4HF6IU1D | ||
KEGG[4] | D00513 | ||
ChEBI | CHEBI:8214 | ||
ChEMBL[5] | CHEMBL500 | ||
Hemijski podaci | |||
Formula | C14H20N2O2 | ||
Mol. masa | 248,321 g/mol | ||
SMILES | eMolekuli & PubHem | ||
| |||
Farmakokinetički podaci | |||
Bioraspoloživost | 50% do 95% | ||
Metabolizam | Hepatički | ||
Poluvreme eliminacije | 3–4 sata | ||
Izlučivanje | Renalno | ||
Farmakoinformacioni podaci | |||
Trudnoća | C(AU) B(US) | ||
Pravni status | ℞ Prescription only | ||
Način primene | oralno, iv |
Farmakologija
urediPindolol je neselektivni beta blokator sa parcijalnom beta-adrenergičkom aktivnošću. On manifestuje intrizičku simpatomimetičku aktivnost. Drugim rečima pindolol, posebno u visokim dozama, ispoljava efekte poput epinefrina ili izoprenalina (povošeni puls i krvni pristisa, bronhodilatacija), mada su ti efekti ograničeni. Pindolol takođe pokazuje membransko stabilišuće dejstvo poput hinidina. On takođe funkcioniše kao slab parcijalni agonist / antagonist 5-HT1A receptora.
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.
- ↑ 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.
- ↑ 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.