Synthesis and structure-activity relations of bestatin analogs, inhibitors of aminopeptidase B

R Nishizawa, T Saino, T Takita, H Suda…

Index: Takita,T. et al. Journal of Medicinal Chemistry, 1977 , vol. 20, p. 510 - 515

Full Text: HTML

Citation Number: 171

Abstract

Stereoisomers and analogues of bestatin,[(2S, 3R)-3-amino-2-hydroxy-4-phenylbutanoyl]-~- leucine, were synthesized and tested for aminopeptidase B and leucine aminopeptidase inhibiting activity. Among the eight stereoisomers, the 2s stereoisomers exhibited strong activity. In a series of compounds in which the L-leucine residue of bestatin was substituted with other amino acids, only the one containing isoleucine showed more activity than ...

Related Articles:

An improved one-pot method for the stereoselective synthesis of the (2S, 3R)-3-amino-2-hydroxy acids: key intermediates for bestatin and amastatin

[Herranz; Castro-Pichel; Vinuesa; Garcia-Lopez Journal of Organic Chemistry, 1990 , vol. 55, # 7 p. 2232 - 2234]

An improved one-pot method for the stereoselective synthesis of the (2S, 3R)-3-amino-2-hydroxy acids: key intermediates for bestatin and amastatin

[Herranz; Castro-Pichel; Vinuesa; Garcia-Lopez Journal of Organic Chemistry, 1990 , vol. 55, # 7 p. 2232 - 2234]

More Articles...