NEW INHIBITORS OF HUMAN RENIN THAT CONTAIN NOVEL REPLACEMENTS AT THE P2 SITE
被引:25
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DOHERTY, AM
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
DOHERTY, AM
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KALTENBRONN, JS
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
KALTENBRONN, JS
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HUDSPETH, JP
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
HUDSPETH, JP
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REPINE, JT
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
REPINE, JT
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ROARK, WH
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
ROARK, WH
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SIRCAR, I
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
SIRCAR, I
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TINNEY, FJ
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
TINNEY, FJ
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CONNOLLY, CJ
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
CONNOLLY, CJ
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HODGES, JC
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
HODGES, JC
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TAYLOR, MD
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
TAYLOR, MD
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BATLEY, BL
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
BATLEY, BL
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RYAN, MJ
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
RYAN, MJ
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ESSENBURG, AD
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
ESSENBURG, AD
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RAPUNDALO, ST
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
RAPUNDALO, ST
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WEISHAAR, RE
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
WEISHAAR, RE
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HUMBLET, C
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
HUMBLET, C
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LUNNEY, EA
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WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USAWARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
LUNNEY, EA
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机构:
[1] WARNER LAMBERT PARKE DAVIS, PARKE DAVIS PHARMACEUT RES DIV,DEPT PHARMACOL, ANN ARBOR, MI 48105 USA
A series of renin inhibitors with novel modifications at the P2 site has been prepared. Structure-activity relationships reveal that for a particular P2 fragment the in vitro potency is highly dependent on the nature of the P2' portion in addition to the P1-P1' group. The length of the P2 side chain and choice of epsilon-N P2 substitution have been found to be important for in vitro potency although the degree of unsaturation in the P2 side chain is not particularly significant. Molecular modeling studies have shown that it is possible for the P2 side chain to interact unfavorably with the P2' binding site. It has been possible to control the specificity for renin over cathepsin D by correct modification at the P2' and P1-P1' sites. Variations at the P4 site have been utilized to lower the log P values of these renin inhibitors while maintaining high potency. Compound 42, which exhibited an IC50 of 3.70 nM, log P of 2.3, and showed high specificity for renin, was selected for further studies. It was found to be very stable under neutral, acidic, and basic conditions. In simulated intestinal juice, compound 42 had a half-life of 37 min while it was virtually unaffected by simulated gastric juice after 4 h. Compound 42 produced a significant hypotensive response upon intravenous administration to the salt-depleted normotensive cynomolgus monkey.