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Merck
  • Nonpeptide glycoprotein IIB/IIIA inhibitors. 19. A new design paradigm employing linearly minimized, centrally constrained, exosite inhibitors.

Nonpeptide glycoprotein IIB/IIIA inhibitors. 19. A new design paradigm employing linearly minimized, centrally constrained, exosite inhibitors.

Bioorganic & medicinal chemistry letters (1999-04-17)
G D Hartman, M E Duggan, W F Hoffman, R J Meissner, J J Perkins, A E Zartman, A M Naylor-Olsen, J J Cook, J D Glass, R J Lynch, G Zhang, R J Gould
摘要

A new series of potent, linearly-minimized, orally active, selective GPIIb/IIIa inhibitors is identified. Thus 15 (L-750,034) achieves interaction via a constrained, non-turned conformation that maintains the proper distance between its charged termini and full sulfonamide exosite interaction. The diminutive stature and the proposed linear conformation of L-750,034 define a new paradigm for the conceptualization of RGD mimics.

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Sigma-Aldrich
4-羟基苯甲酰胺, 98%