Insulin aspart
(Preusmjereno sa stranice VOMXSOIBEJBQNF-UTTRGDHVSA-N)
Insulin aspart je rekombinantni, biosintetički, brzo delujući analog insulina. On ima jednu aminokiselinsku supstituciju u poziciji B28, gde je prolin zamenjen aspartičkom kiselinom. Ta supstitucija umanjuje sklonost insulina da formira heksamere i daje mu veći stepen apsorpcije nakon potkožne administracije u odnosu na prirodni insulin. Insulin aspart se proizvodi u genetički modifikovanoj vrsti kvasca Saccharomyces cerevisiae.[4][5][6][7]
Klinički podaci | |||
---|---|---|---|
Robne marke | NovoLog, Novolog FlexPen, Novolog Penfill, NovoRapid | ||
AHFS/Drugs.com | aspart.html Monografija | ||
Identifikatori | |||
CAS broj | 116094-23-6 | ||
ATC kod | A10AB05 , A10AD05 | ||
PubChem[1][2] | 16132418 | ||
DrugBank | DB01306 | ||
ChEMBL[3] | CHEMBL1201496 | ||
Hemijski podaci | |||
Formula | C256H381N65O79S6 | ||
Mol. masa | 5825.8 | ||
SMILES | eMolekuli & PubHem | ||
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Farmakokinetički podaci | |||
Poluvreme eliminacije | 81 minuta | ||
Farmakoinformacioni podaci | |||
Trudnoća | ? | ||
Pravni status | |||
Način primene | Subkutano |
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.
- ↑ 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.
- ↑ Heller S, Kurtzhals P, Verge D, Lindholm A: Insulin aspart: promising early results borne out in clinical practice. Expert Opin Pharmacother. 2002 Feb;3(2):183-95. PMID 11829732
- ↑ Sciacca L, Cassarino MF, Genua M, Pandini G, Le Moli R, Squatrito S, Vigneri R: Insulin analogues differently activate insulin receptor isoforms and post-receptor signalling. Diabetologia. 2010 Apr 28. PMID 20424816
- ↑ Knox C, Law V, Jewison T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS (2011). „DrugBank 3.0: a comprehensive resource for omics research on drugs”. Nucleic Acids Res. 39 (Database issue): D1035-41. DOI:10.1093/nar/gkq1126. PMC 3013709. PMID 21059682.
- ↑ David S. Wishart, Craig Knox, An Chi Guo, Dean Cheng, Savita Shrivastava, Dan Tzur, Bijaya Gautam, and Murtaza Hassanali (2008). „DrugBank: a knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Res 36 (Database issue): D901-6. DOI:10.1093/nar/gkm958. PMC 2238889. PMID 18048412.
Literatura
uredi- 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.
- Thomas L. Lemke, David A. Williams, ur. (2007). Foye's Principles of Medicinal Chemistry (6 izd.). Baltimore: Lippincott Willams & Wilkins. ISBN 0-7817-6879-9.