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For a similar study on diaryl pyrazoles, see:
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523) in COX-2. See: These substituents usually confer optimal COX-2 inhibitory potency when one of them is present at the para position of one aryl ring. See:
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523) in COX-2. See: Loung C., Miller A., Barnett J., Chow J., Ramesha C., Browner M.F. Nat. Struct. Biol. 3:1996;927 (b) . These substituents usually confer optimal COX-2 inhibitory potency when one of them is present at the para position of one aryl ring. See: Khanna I.K., Weier R.M., Yu Y., Collins P.W., Miyashiro J.M., Koboldt C.M., Veenhuizen A.W., Currie J.L., Seibert K., Isakson P.C. J. Med. Chem. 40:1997;1619.
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13b generated from 2-(4-methylsulfanylphenyl)acetic acid and appropriate bromoketone (obtained by bromination of 1-phenyl-1-butanone) followed by oxidation of the methylsulfanyl moiety to methanesulfone.
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