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Volumn 42, Issue 1, 1999, Pages 164-172

Carboxy-substituted cinnamides: A novel series of potent, orally active LTB4 receptor antagonists

Author keywords

[No Author keywords available]

Indexed keywords

CINNAMAMIDE DERIVATIVE; CINNAMIC ACID DERIVATIVE; LEUKOTRIENE B4; LEUKOTRIENE B4 RECEPTOR ANTAGONIST; MOXILUBANT MALEATE; MYELOPEROXIDASE; PHENYLCINNAMIDE; UNCLASSIFIED DRUG;

EID: 0033552867     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm980540v     Document Type: Article
Times cited : (14)

References (31)
  • 5
    • 0021352632 scopus 로고
    • 4 by colonic mucosa in inflammatory bowel disease
    • 4 by colonic mucosa in inflammatory bowel disease. Gastroenterology 1984, 86, 453-460.
    • (1984) Gastroenterology , vol.86 , pp. 453-460
    • Sharon, P.1    Stenson, W.F.2
  • 9
    • 0030021571 scopus 로고    scopus 로고
    • 4 receptor antagonists: Recent clinical developments
    • 4 receptor antagonists: recent clinical developments. Exp. Opin. Invest. Drugs 1996, 5, 73-77.
    • (1996) Exp. Opin. Invest. Drugs , vol.5 , pp. 73-77
    • Sawyer, J.S.1
  • 16
    • 0000702671 scopus 로고
    • Palladium catalyzed vinylations of organic halides
    • Heck, R. Palladium catalyzed vinylations of organic halides. Org. Reactions 1982, 27, 345-390.
    • (1982) Org. Reactions , vol.27 , pp. 345-390
    • Heck, R.1
  • 17
    • 0001467068 scopus 로고
    • Selective alkylations of certain phenolic and enolic functions with lithium carbonate/alkyl halide
    • Wymann, W. E.; Davis, R.; Patterson, J. W.; Pfister, J. R. Selective alkylations of certain phenolic and enolic functions with lithium carbonate/alkyl halide. Synth. Commun. 1988, 18, 1379-1384.
    • (1988) Synth. Commun. , vol.18 , pp. 1379-1384
    • Wymann, W.E.1    Davis, R.2    Patterson, J.W.3    Pfister, J.R.4
  • 18
    • 0027180141 scopus 로고
    • Synthetic transformations of vinyl and aryl triflates
    • Ritter, K. Synthetic transformations of vinyl and aryl triflates. Synthesis 1993, 735-753.
    • (1993) Synthesis , pp. 735-753
    • Ritter, K.1
  • 19
    • 0026574079 scopus 로고
    • Directed ortho metalation of O-aryl and O-pyridyl thiocarbamates. A versatile synthetic method for substituted phenol into thiophenol conversion
    • Beaulieu, F.; Snieckus, V. Directed ortho metalation of O-aryl and O-pyridyl thiocarbamates. A versatile synthetic method for substituted phenol into thiophenol conversion. Synthesis 1992, 112-118.
    • (1992) Synthesis , pp. 112-118
    • Beaulieu, F.1    Snieckus, V.2
  • 20
    • 0023755363 scopus 로고
    • Chiral synthesis via organoboranes. 18. Selective reductions. 43. Diisoprinocampheylchloroborane as an excellent chiral reducing reagent for the synthesis of halo alcohols of high enantiomeric purity. A highly enantioselective synhteisis of both optical isomers of tom oxetine, fluoxetine, and nisoxetine
    • Srebnik, M.; Ramachandran, P. V.; Brown, H. C. Chiral synthesis via organoboranes. 18. Selective reductions. 43. Diisoprinocampheylchloroborane as an excellent chiral reducing reagent for the synthesis of halo alcohols of high enantiomeric purity. A highly enantioselective synhteisis of both optical isomers of tom oxetine, fluoxetine, and nisoxetine. J. Org. Chem. 1988, 53, 2916-2920.
    • (1988) J. Org. Chem. , vol.53 , pp. 2916-2920
    • Srebnik, M.1    Ramachandran, P.V.2    Brown, H.C.3
  • 21
    • 0344328240 scopus 로고    scopus 로고
    • note
    • 1H NMRs were taken of racemic and optically enriched materials in a mixture with (R)-naphthylethylamine. See Experimental Section for details.
  • 22
    • 84985609802 scopus 로고
    • Catalytic hydroborations with rhodium complexes
    • Manning, D.; Noth, H. Catalytic hydroborations with rhodium complexes. Angew. Chem., Int. Ed. Engl. 1985, 24, 878-879.
    • (1985) Angew. Chem., Int. Ed. Engl. , vol.24 , pp. 878-879
    • Manning, D.1    Noth, H.2
  • 24
    • 0344760254 scopus 로고    scopus 로고
    • note
    • Note that, as this study progressed, some of the less stringent in vivo assays were phased out. For this reason, many of the later compounds do not have in vivo data for the earlier time points.
  • 27
    • 0023393182 scopus 로고
    • Fluorometer based multi-parameter analysis of phagocytic cell activation
    • Seligmann, B.; Patel, K.; Haston, W. O.; Rediske, J. J. Fluorometer based multi-parameter analysis of phagocytic cell activation. Agents Actions 1987, 21, 375-378.
    • (1987) Agents Actions , vol.21 , pp. 375-378
    • Seligmann, B.1    Patel, K.2    Haston, W.O.3    Rediske, J.J.4
  • 28
    • 0021068970 scopus 로고
    • Comparative responses of human poylmorphonclear leukocytes obtained by counterflow centrifugal elutriation and Ficoll-Hypaque density centrifugation
    • Berkow, R. L.; Weisman, S. J.; Tzeng, D.; Williams, L. V.; Baehner, R. L. Comparative responses of human poylmorphonclear leukocytes obtained by counterflow centrifugal elutriation and Ficoll-Hypaque density centrifugation. J. Lab. Clin. Med. 1984, 102, 732-742.
    • (1984) J. Lab. Clin. Med. , vol.102 , pp. 732-742
    • Berkow, R.L.1    Weisman, S.J.2    Tzeng, D.3    Williams, L.V.4    Baehner, R.L.5
  • 30
    • 0027171416 scopus 로고
    • Effect of antiinflammatory compounds on edema formation and myeloperoxidase activity in the arachidonic acid-induced ear model in the mouse
    • Kotyuk, B.; Raychaudhuri, A.; DiPasquale, G. Effect of antiinflammatory compounds on edema formation and myeloperoxidase activity in the arachidonic acid-induced ear model in the mouse. Agents Actions 1993, 39, C46-C48.
    • (1993) Agents Actions , vol.39
    • Kotyuk, B.1    Raychaudhuri, A.2    DiPasquale, G.3
  • 31
    • 0022442643 scopus 로고
    • Reaction of lithiated senecioamide and related compounds with benzynes: Efficient syntheses of naphthols and naphthoquinones
    • Watanabe, M.; Hisamatsu, S.; Hotokezaka, H.; Furukawa, S. Reaction of lithiated senecioamide and related compounds with benzynes: efficient syntheses of naphthols and naphthoquinones. Chem. Pharm. Bull. 1986, 34, 2810-2820.
    • (1986) Chem. Pharm. Bull. , vol.34 , pp. 2810-2820
    • Watanabe, M.1    Hisamatsu, S.2    Hotokezaka, H.3    Furukawa, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.