Tirofiban
| Clinical data | |
|---|---|
| Trade names | Aggrastat |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a601210 |
| License data | |
| Pregnancy category |
|
| Routes of administration | intravenous |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Protein binding | 65% |
| Elimination half-life | 2 hours |
| Identifiers | |
| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | |
| ChemSpider | |
| UNII | |
| KEGG | |
| ChEBI | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.163.548 |
| Chemical and physical data | |
| Formula | C22H36N2O5S |
| Molar mass | 440.60 g·mol−1 |
| 3D model (JSmol) | |
SMILES
| |
InChI
| |
| (verify) | |
Tirofiban, sold under the brand name Aggrastat, is an antiplatelet medication. It belongs to a class of antiplatelets named glycoprotein IIb/IIIa inhibitors. Tirofiban is a small molecule inhibitor of the protein-protein interaction between fibrinogen and the platelet integrin receptor GP IIb/IIIa and is the first drug candidate whose origins can be traced to a pharmacophore-based virtual screening lead.[2][3]
It is available as a generic medication.[4]
- ^ "Aggrastat- tirofiban injection, solution". DailyMed. Retrieved 19 June 2021.
- ^ Hartman GD, Egbertson MS, Halczenko W, Laswell WL, Duggan ME, Smith RL, et al. (November 1992). "Non-peptide fibrinogen receptor antagonists. 1. Discovery and design of exosite inhibitors". Journal of Medicinal Chemistry. 35 (24). American Chemical Society: 4640–2. doi:10.1021/jm00102a020. PMID 1469694.
- ^ Van Drie JH (2007). "Computer-aided drug design: the next 20 years". Journal of Computer-Aided Molecular Design. 21 (10–11). Springer: 591–601. Bibcode:2007JCAMD..21..591V. doi:10.1007/s10822-007-9142-y. PMID 17989929. S2CID 3060340.
- ^ "First Generic Drug Approvals 2023". U.S. Food and Drug Administration (FDA). 30 May 2023. Archived from the original on 30 June 2023. Retrieved 30 June 2023.