Journal of Medicinal Chemistry 1992-05-15

HIV-1 protease inhibitors based on hydroxyethylene dipeptide isosteres: an investigation into the role of the P1' side chain on structure-activity.

S D Young, L S Payne, W J Thompson, N Gaffin, T A Lyle, S F Britcher, S L Graham, T H Schultz, A A Deana, P L Darke

Index: J. Med. Chem. 35 , 1702, (1992)

Full Text: HTML

Abstract

A systematic investigation was undertaken to determine the role of the P1' sidechain in a series of hydroxyethylene isostere based inhibitors of HIV-1 protease. Substitution and homologation of the benzyl P1' side chain of the Phe-Phe isostere based pseudo peptides 1 (L-682,679) and 2 (L-685,434) with various heteroalkyl groups leads to a series of extremely potent inhibitors of the enzyme. Several examples of the most potent inhibitors were very effective in an ex vivo cell based viral spread assay using human H9 T-lymphocytes and the IIIb isolate of HIV-1. Compound 19 is 120 times more potent than 1 and 16 times more potent than 2 in inhibiting the spread of infection in this assay.

Related Compounds

Related Articles:

A series of potent HIV-1 protease inhibitors containing a hydroxyethyl secondary amine transition state isostere: synthesis, enzyme inhibition, and antiviral activity.

1992-07-10

[J. Med. Chem. 35 , 2525, (1992)]

Synthesis and antiviral activity of a series of HIV-1 protease inhibitors with functionality tethered to the P1 or P1' phenyl substituents: X-ray crystal structure assisted design.

1992-05-15

[J. Med. Chem. 35 , 1685, (1992)]

Inhibitors of the protease from human immunodeficiency virus: synthesis, enzyme inhibition, and antiviral activity of a series of compounds containing the dihydroxyethylene transition-state isostere.

1993-04-16

[J. Med. Chem. 36 , 941, (1993)]

D'Aniello, F. et al.

[J. Org. Chem. 59 , 3762, (1994)]

Dorsey, B.D. et al.

[Tetrahedron Lett. 34 , 1851, (1993)]

More Articles...