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Merck

Selective and orally bioavailable phenylglycine tissue factor/factor VIIa inhibitors.

Bioorganic & medicinal chemistry letters (2005-10-11)
Katrin Groebke Zbinden, Ulrike Obst-Sander, Kurt Hilpert, Holger Kühne, David W Banner, Hans-Joachim Böhm, Martin Stahl, Jean Ackermann, Leo Alig, Lutz Weber, Hans Peter Wessel, Markus A Riederer, Thomas B Tschopp, Thierry Lavé
ABSTRAKT

We describe the structure-based design and synthesis of highly potent, orally bioavailable tissue factor/factor VIIa inhibitors which interfere with the coagulation cascade by selective inhibition of the extrinsic pathway.

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Sigma-Aldrich
2-Phenylglycine, 95%
Sigma-Aldrich
L−(+)-α-Phenylglycine, 99%
Sigma-Aldrich
D−(−)-α-Phenylglycine, 99%