Fradafiban
Fradafiban Basic information
- Product Name:
- Fradafiban
- Synonyms:
-
- Fradafiban
- BIBU-52
- 3-Pyrrolidineacetic acid, 5-[[[4'-(aminoiminomethyl)[1,1'-biphenyl]-4-yl]oxy]methyl]-2-oxo-, (3S,5S)-
- Fradafiban/BIBU-52
- CAS:
- 148396-36-5
- MF:
- C20H21N3O4
- MW:
- 367.403
- Mol File:
- 148396-36-5.mol
Fradafiban Chemical Properties
- Density
- 1.38±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in DMSO
- pka
- 4.29±0.10(Predicted)
Fradafiban Usage And Synthesis
Uses
Fradafiban is a nonpeptide platelet glycoprotein IIb/IIIa antagonist, which binds to the human platelet GP IIb/IIIa complex with a Kd value of 148 nM.
Definition
ChEBI: A pyrrolidinone that is pyrrolidin-2-one which is substituted at positions 3 and 5 by carboxymethyl and hydroxymethyl groups, respectively, and in which the hydrogen of the resulting alcoholic hydroxy group is replaced by a 4'-carbamimidoylbiphenyl-4-yl gr up (the S,S-diastereoisomer). A figrinogen receptor antagonist.
in vivo
Fradafiban has only very limited oral activity probably due to its high polarity and thus poor absorption after oral ingestion[1].
References
[1] Müller TH, et al. Profound and sustained inhibition of platelet aggregation by Fradafiban, a nonpeptide platelet glycoprotein IIb/IIIa antagonist, and its orally active prodrug, Lefradafiban, in men. Circulation. 1997 Aug 19;96(4):1130-8. DOI:10.1161/01.cir.96.4.1130
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