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Volumn 10, Issue 12, 2002, Pages 3787-3805

Highly potent inhibitors of TNF-α production. Part II: Metabolic stabilization of a newly found chemical lead and conformational analysis of an active diastereoisomer

Author keywords

[No Author keywords available]

Indexed keywords

1 (OCTANOYLAMINO) 2,3 DIHYDRO 1H INDEN 2 YLDISODIUM PHOSPHATE; 1 METHYL 2 (3 METHOXYPHENYL) 2 (OCTANOYLAMINO)ETHYLDISODIUM PHOSPHATE; 1 METHYL 2 [(HEXYLOXYCARBONYL)AMINO] 2 (3 METHOXYPHENYL)ETHYLDISODIUM PHOSPHATE; 2 (3 ISOPROPYLOXYPHENYL) 1 METHYL 2 (OCTANOYLAMINO)ETHYLDISODIUM PHOSPHATE; ANTIINFLAMMATORY AGENT; GALACTOSAMINE; INDAN DERIVATIVE; PREDNISOLONE; PROTEIN SYNTHESIS INHIBITOR; TUMOR NECROSIS FACTOR ALPHA; UNCLASSIFIED DRUG;

EID: 0036976021     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(02)00380-2     Document Type: Article
Times cited : (24)

References (23)
  • 1
    • 0031946293 scopus 로고    scopus 로고
    • (a) Camussi G., Lupia E. Drugs. 55:1998;613 (b) Arrieta O., Rodriguez-Reyna T.S., Sotelo J. Exp. Opin. Ther. Patents. 10:2000;601.
    • (1998) Drugs , vol.55 , pp. 613
    • Camussi, G.1    Lupia, E.2
  • 3
    • 18344390232 scopus 로고    scopus 로고
    • (a) Matsui T., Kondo T., Nishita Y., Itadani S., Nakatani S., Omawari N., Sakai M., Nakazawa S., Ogata A., Ohno H., Obata T., Nakai H., Toda M. Bioorg. Med. Chem. Lett. 12:2002;903 (b) Matsui T., Kondo T., Nishita Y., Itadani S., Tsuruta H., Fujita S., Omawari N., Sakai M., Nakazawa S., Ogata A., Mori H., Ohno H., Obata T., Nakai H., Toda M. Bioorg. Med. Chem. Lett. 12:2002;907 (c) Matsui, T.; Kondo, T.; Nishita, Y.; Itadani, S.; Nakatani, S.; Omawari, N.; Sakai, M.; Nakazawa, S.; Ogata, A.; Mori, H.; Terai, K.; Kamoshima, W.; Ohno, H.; Obata, T.; Nakai, H.; Toda, M. Bioorg. Med. Chem. Accepted for publication.
    • (2002) Bioorg. Med. Chem. Lett. , vol.12 , pp. 903
    • Matsui, T.1    Kondo, T.2    Nishita, Y.3    Itadani, S.4    Nakatani, S.5    Omawari, N.6    Sakai, M.7    Nakazawa, S.8    Ogata, A.9    Ohno, H.10    Obata, T.11    Nakai, H.12    Toda, M.13
  • 5
    • 0012973373 scopus 로고    scopus 로고
    • Accepted for publication
    • (a) Matsui T., Kondo T., Nishita Y., Itadani S., Nakatani S., Omawari N., Sakai M., Nakazawa S., Ogata A., Ohno H., Obata T., Nakai H., Toda M. Bioorg. Med. Chem. Lett. 12:2002;903 (b) Matsui T., Kondo T., Nishita Y., Itadani S., Tsuruta H., Fujita S., Omawari N., Sakai M., Nakazawa S., Ogata A., Mori H., Ohno H., Obata T., Nakai H., Toda M. Bioorg. Med. Chem. Lett. 12:2002;907 (c) Matsui, T.; Kondo, T.; Nishita, Y.; Itadani, S.; Nakatani, S.; Omawari, N.; Sakai, M.; Nakazawa, S.; Ogata, A.; Mori, H.; Terai, K.; Kamoshima, W.; Ohno, H.; Obata, T.; Nakai, H.; Toda, M. Bioorg. Med. Chem. Accepted for publication.
    • Matsui, T.1    Kondo, T.2    Nishita, Y.3    Itadani, S.4    Tsuruta, H.5    Fujita, S.6    Omawari, N.7    Sakai, M.8    Nakazawa, S.9    Ogata, A.10    Mori, H.11    Ohno, H.12    Obata, T.13    Nakai, H.14    Toda, M.15
  • 6
    • 0029937757 scopus 로고    scopus 로고
    • (a) Chag H.-T., Sharpless K.B. Tetrahedron Lett. 37:1996;3219 (b) Kolb H.C., VanNieuwenhze M.S., Sharpless K.B. Chem. Rev. 94:1994;2483.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3219
    • Chag, H.-T.1    Sharpless, K.B.2
  • 8
    • 0001815649 scopus 로고
    • (a) Dibenzylphosphorochloridate was prepared from benzyl phenoxymethylphosphinate according to the following paper and used as 1 M stock solution: Kenner, G. W.; Todd, A. R.; Weymouth, F. J. J. Chem. Soc. 1952, 3675. (b) Rasolonjaatovo I., Sarfati S.R. Nucleosides & Nucleotides. 17:1998;2021. and references cited therein (c) Ozaki S., Ling L., Ogasawara T., Watanabe Y., Hirata M. Carbohydr. Res. 259:1994;307.
    • (1952) J. Chem. Soc. , pp. 3675
    • Kenner, G.W.1    Todd, A.R.2    Weymouth, F.J.3
  • 9
    • 0031789467 scopus 로고    scopus 로고
    • (a) Dibenzylphosphorochloridate was prepared from benzyl phenoxymethylphosphinate according to the following paper and used as 1 M stock solution: Kenner, G. W.; Todd, A. R.; Weymouth, F. J. J. Chem. Soc. 1952, 3675. (b) Rasolonjaatovo I., Sarfati S.R. Nucleosides & Nucleotides. 17:1998;2021. and references cited therein (c) Ozaki S., Ling L., Ogasawara T., Watanabe Y., Hirata M. Carbohydr. Res. 259:1994;307.
    • (1998) Nucleosides & Nucleotides , vol.17 , pp. 2021
    • Rasolonjaatovo, I.1    Sarfati, S.R.2
  • 10
    • 0028455039 scopus 로고
    • and references cited therein
    • (a) Dibenzylphosphorochloridate was prepared from benzyl phenoxymethylphosphinate according to the following paper and used as 1 M stock solution: Kenner, G. W.; Todd, A. R.; Weymouth, F. J. J. Chem. Soc. 1952, 3675. (b) Rasolonjaatovo I., Sarfati S.R. Nucleosides & Nucleotides. 17:1998;2021. and references cited therein (c) Ozaki S., Ling L., Ogasawara T., Watanabe Y., Hirata M. Carbohydr. Res. 259:1994;307.
    • (1994) Carbohydr. Res. , vol.259 , pp. 307
    • Ozaki, S.1    Ling, L.2    Ogasawara, T.3    Watanabe, Y.4    Hirata, M.5
  • 14
    • 0002618711 scopus 로고
    • Compound 41 was prepared from 3-benzyloxy benzaldehyde according to the following paper: Steiger, R. E. Org. Synth., 1995, III 84.
    • (1995) Org. Synth. , vol.3 , pp. 84
    • Steiger, R.E.1
  • 23
    • 0013012965 scopus 로고    scopus 로고
    • note
    • See Experimental.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.