Abstract

Two types of P1-P3-linked macrocyclic renin inhibitors containing the hydroxyethylene isostere (HE) scaffold just outside the macrocyclic ring have been synthesized. An aromatic or aliphatic substituent (P3sp) was introduced in the macrocyclic ring aiming at the S3 subpocket (S3sp) in order to optimize the potency. A 5-6-fold improvement in both the K(i) and the human plasma renin activity (HPRA) IC(50) was observed when moving from the starting linear peptidomimetic compound 1 to the most potent macrocycle 42 (K(i) = 3.3 nM and HPRA IC(50) = 7 nM). Truncation of the prime side of 42 led to 8-10-fold loss of inhibitory activity in macrocycle 43 (K(i) = 34 nM and HPRA IC(50) = 56 nM). All macrocycles were epimeric mixtures in regard to the P3sp substituent and X-ray crystallographic data of the representative renin macrocycle 43 complex showed that only the S-isomer buried the substituent into the S3sp. Inhibitory selectivity over cathepsin D (Cat-D) and BACE-1 was also investigated for all the macrocycles and showed that truncation of the prime side increased selectivity of inhibition in favor of renin. (C) 2010 Elsevier Ltd. All rights reserved.

Keywords

Renin; Aspartyl protease; Macrocycle; Antihypertensive; Peptidomimetic; Cathepsin D; BACE-1

Published in

Bioorganic and Medicinal Chemistry Letters
2011, Volume: 21, number: 1, pages: 358-362
Publisher: PERGAMON-ELSEVIER SCIENCE LTD

UKÄ Subject classification

Medicinal Chemistry


Publication identifier

DOI: https://doi.org/10.1016/j.bmcl.2010.10.140

Permanent link to this page (URI)

https://res.slu.se/id/publ/99465