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 inBioorganic & medicinal chemistry letters Vol. 17; no. 11; pp. 3006 - 3009
Main Authors Su, Dai-Shi, Lim, John L, Markowitz, MKristine, Wan, Bang-Lin, Murphy, Kathy L, Reiss, Duane R, Harrell, CMeacham, O'Malley, Stacy S, Ransom, Rick W, Chang, Raymond SL, Pettibone, Douglas J, Tang, Cuyue, Prueksaritanont, Thomayant, Freidinger, Roger M, Bock, Mark G
Format Journal Article
LanguageEnglish
Published 01.06.2007
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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.
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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