C32-amino derivatives of the immunosuppressant ascomycin

Bioorganic & Medicinal Chemistry Letters
1997.0

Abstract

Various C32-amino derivatives were investigated as replacements for the C32-hydroxyl group of ascomycin and its C24-deoxy analog. The syntheses of these amino derivatives and their biological evaluation are reported herein.

Knowledge Graph

Similar Paper

C32-amino derivatives of the immunosuppressant ascomycin
Bioorganic & Medicinal Chemistry Letters 1997.0
Potent immunosuppressive C32-O-arylethyl ether derivatives of ascomycin with reduced toxicity
Bioorganic & Medicinal Chemistry Letters 1999.0
C32-O-imidazol-2-yl-methyl ether derivatives of the immunosuppressant ascomycin with improved therapeutic potential
Bioorganic & Medicinal Chemistry Letters 1998.0
Preparation and immunosuppressive activity of 32-(O)-acylated and 32-(O)-thioacylated analogues of ascomycin
Bioorganic & Medicinal Chemistry Letters 1999.0
Studies on an immunosuppressive macrolactam, ascomycin: Synthesis of a C-33 hydroxyl derivative
Bioorganic & Medicinal Chemistry Letters 1998.0
C32-O-phenalkyl ether derivatives of the immunosuppressant ascomycin: a tether length study
Bioorganic & Medicinal Chemistry Letters 1999.0
32-Ascomycinyloxyacetic Acid Derived Immunosuppressants. Independence of Immunophilin Binding and Immunosuppressive Potency
Journal of Medicinal Chemistry 1998.0
Alkyl ether derivatives of the FK-506 related, immunosuppressive macrolide L-683,742 (C31-O-desmethyl ascomycin)
Bioorganic & Medicinal Chemistry Letters 1994.0
Alkyl ether analogs of the FK-506 related, immunosuppressive macrolide L-683,590 (ascomycin)
Bioorganic & Medicinal Chemistry Letters 1994.0
Retention of Immunosuppressant Activity in an Ascomycin Analogue Lacking a Hydrogen-Bonding Interaction with FKBP12
Journal of Medicinal Chemistry 1999.0