Potent bradykinin B sub(1) receptor antagonists: 4-Substituted phenyl cyclohexanes
Selective bradykinin (BK) B sub(1) receptor antagonists have been shown to be antinociceptive in animal models and could be novel therapeutic agents for the treatment of pain and inflammation. Elucidation of the structure-activity relationships of the biphenyl moiety of the lead compound 1 provided...
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Published in | Bioorganic & medicinal chemistry letters Vol. 17; no. 11; pp. 3006 - 3009 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.06.2007
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Online Access | Get full text |
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Abstract | Selective bradykinin (BK) B sub(1) receptor antagonists have been shown to be antinociceptive in animal models and could be novel therapeutic agents for the treatment of pain and inflammation. Elucidation of the structure-activity relationships of the biphenyl moiety of the lead compound 1 provided a potent new structural class of BK B sub(1) receptor antagonists. |
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AbstractList | Selective bradykinin (BK) B sub(1) receptor antagonists have been shown to be antinociceptive in animal models and could be novel therapeutic agents for the treatment of pain and inflammation. Elucidation of the structure-activity relationships of the biphenyl moiety of the lead compound 1 provided a potent new structural class of BK B sub(1) receptor antagonists. |
Author | Freidinger, Roger M Markowitz, MKristine Ransom, Rick W Harrell, CMeacham Lim, John L Chang, Raymond SL O'Malley, Stacy S Tang, Cuyue Murphy, Kathy L Prueksaritanont, Thomayant Su, Dai-Shi Pettibone, Douglas J Reiss, Duane R Wan, Bang-Lin Bock, Mark G |
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Title | Potent bradykinin B sub(1) receptor antagonists: 4-Substituted phenyl cyclohexanes |
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