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Volumn 13, Issue 10, 2003, Pages 1639-1643

Conformationally restricted 3,4-diarylfuranones (2,3a,4,5-tetrahydronaphthofuranones) as selective cyclooxygenase-2 inhibitors

Author keywords

[No Author keywords available]

Indexed keywords

5 ETHYL 3 (4 METHYLSULFONYLPHENYL) 4 PHENYL 2,5 DIHYDRO 2 FURANONE; CYCLOOXYGENASE 2 INHIBITOR; FURANONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0038363943     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(03)00282-8     Document Type: Article
Times cited : (56)

References (28)
  • 14
    • 0035974649 scopus 로고    scopus 로고
    • Replacement of methylsulfonyl moiety by other groups including azido bioisostere and their subsequent effect on COX activity has been reported; see, for example: and references cited therein
    • Replacement of methylsulfonyl moiety by other groups including azido bioisostere and their subsequent effect on COX activity has been reported; see, for example: Habeeb A.G., Praveen Rao P.N., Knaus E.E. J. Med. Chem. 44:2001;3039. and references cited therein.
    • (2001) J. Med. Chem. , vol.44 , pp. 3039
    • Habeeb, A.G.1    Praveen Rao, P.N.2    Knaus, E.E.3
  • 16
    • 0000224843 scopus 로고    scopus 로고
    • Pal, M.; Rao, Y. K.; Rajagopalan, R.; Misra, P.; Kumar, P. M.; Rao, C. S. World Patent WO 01/90097, Nov. 29, 2001; Chem. Abstr. 2002, 136, 5893.
    • (2002) Chem. Abstr. , vol.136 , pp. 5893
  • 24
    • 0029911267 scopus 로고    scopus 로고
    • 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.
    • (1996) Nat. Struct. Biol. , vol.3 , pp. 927
    • Loung, C.1    Miller, A.2    Barnett, J.3    Chow, J.4    Ramesha, C.5    Browner, M.F.6
  • 25
    • 0030968683 scopus 로고    scopus 로고
    • 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:
    • 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.
    • (1997) J. Med. Chem. , vol.40 , pp. 1619
    • Khanna, I.K.1    Weier, R.M.2    Yu, Y.3    Collins, P.W.4    Miyashiro, J.M.5    Koboldt, C.M.6    Veenhuizen, A.W.7    Currie, J.L.8    Seibert, K.9    Isakson, P.C.10
  • 28
    • 85031193694 scopus 로고    scopus 로고
    • 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.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.