In vitro and in vivo studies on the metabolism of tirofiban.

@article{Vickers1999InVA,
  title={In vitro and in vivo studies on the metabolism of tirofiban.},
  author={Stanley Vickers and Anthony D. Theoharides and Byron H. Arison and Suresh K. Balani and Donghui Cui and Carolyn A Duncan and Joan D. Ellis and L M Gorham and Sarit Polsky and Thomayant Prueksaritanont and Harri G Ramjit and Donald E Slaughter and Kamlesh P Vyas},
  journal={Drug metabolism and disposition: the biological fate of chemicals},
  year={1999},
  volume={27 11},
  pages={1360-6}
}
Tirofiban hydrochloride [L-tyrosine-N-(butylsulfonyl)-O-[4-(4-piperidinebutyl)] monohydrochloride, is a potent and specific fibrinogen receptor antagonist. Radiolabeled tirofiban was synthesized with either (3)H-label incorporated into the phenyl ring of the tyrosinyl residue or (14)C-label in the butane sulfonyl moiety. Neither human liver microsomes nor liver slices metabolized [(14)C]tirofiban. However, male rat liver microsomes converted a limited amount of the substrate to a more polar… CONTINUE READING

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