5-Piperazinyl pyridine carboxamide bradykinin B sub(1) antagonists
A series of 2,3-diaminopyridine bradykinin B sub(1) antagonists was modified to mitigate the potential for bioactivation. Removal of the 3-amino group and incorporation of basic 5-piperazinyl carboxamides at the pyridine 5-position provided compounds with high affinity for the human B sub(1) recepto...
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Published in | Bioorganic & medicinal chemistry letters Vol. 16; no. 10; pp. 2791 - 2795 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2006
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Online Access | Get full text |
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Summary: | A series of 2,3-diaminopyridine bradykinin B sub(1) antagonists was modified to mitigate the potential for bioactivation. Removal of the 3-amino group and incorporation of basic 5-piperazinyl carboxamides at the pyridine 5-position provided compounds with high affinity for the human B sub(1) receptor. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2006.01.112 |