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Volumn 44, Issue 2, 1996, Pages 273-279

Michael-type addition of illudin S, a toxic substance from Lampteromyces japonicus, with cysteine and cysteine-containing peptides in vitro

Author keywords

cysteine methyl ester; illudin S; Lampteromyces japonicus; liquid chromatography tandem mass spectrometry; glutamylcysteinylglycine

Indexed keywords

CYSTEINE DERIVATIVE; CYSTEINYLASPARTYLPROLYLGLYCYLTYROSYLISOLEUCYLGLYCYLSERYLARGININE; GLUTATHIONE; ILLUDIN S; MECYSTEINE; UNCLASSIFIED DRUG;

EID: 0029935497     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.44.273     Document Type: Article
Times cited : (17)

References (18)
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    • Itano T., Okayama Igaku Zasshi, 91, 453-460 (1978); Shinozawa K., Tsutsui K., Oda T , Expertentia, 35, 1102-1103 (1979); Kelner M. J , McMorris T. C., Beck W. T., Zamora J. M., Taetle R., Cancer Res., 47, 3186-3189 (1987).
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    • Itano T., Okayama Igaku Zasshi, 91, 453-460 (1978); Shinozawa K., Tsutsui K., Oda T , Expertentia, 35, 1102-1103 (1979); Kelner M. J , McMorris T. C., Beck W. T., Zamora J. M., Taetle R., Cancer Res., 47, 3186-3189 (1987).
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    • It is well known that many compounds having an α,β-unsaturated carbonyl group form an S-conjugate with endogenous glutathione; Boyland E., Chasseaud L. F., Biochem. J., 109, 651-661 (1968); Chasseaud L.F., ibid., 131, 765-769 (1973).
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    • It is well known that many compounds having an α,β-unsaturated carbonyl group form an S-conjugate with endogenous glutathione; Boyland E., Chasseaud L. F., Biochem. J., 109, 651-661 (1968); Chasseaud L.F., ibid., 131, 765-769 (1973).
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    • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y , Inagaki S., Yakugaku Zasshi, 83, 377-380 (1963); Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H., Nature (London), 197, 292 (1963); Nakanishi K., Tada M., Yamada Y., Chem. Pharm. Bull., 12, 856-857 (1964); Nakanishi K., Ohashi M., Tada M., Yamada Y., Tetrahedron, 21, 1231-1246 (1965); Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M., Chem. Pharm. Bull., 12, 853-855 (1964).
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    • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y , Inagaki S., Yakugaku Zasshi, 83, 377-380 (1963); Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H., Nature (London), 197, 292 (1963); Nakanishi K., Tada M., Yamada Y., Chem. Pharm. Bull., 12, 856-857 (1964); Nakanishi K., Ohashi M., Tada M., Yamada Y., Tetrahedron, 21, 1231-1246 (1965); Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M., Chem. Pharm. Bull., 12, 853-855 (1964).
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    • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y , Inagaki S., Yakugaku Zasshi, 83, 377-380 (1963); Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H., Nature (London), 197, 292 (1963); Nakanishi K., Tada M., Yamada Y., Chem. Pharm. Bull., 12, 856-857 (1964); Nakanishi K., Ohashi M., Tada M., Yamada Y., Tetrahedron, 21, 1231-1246 (1965); Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M., Chem. Pharm. Bull., 12, 853-855 (1964).
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    • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y , Inagaki S., Yakugaku Zasshi, 83, 377-380 (1963); Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H., Nature (London), 197, 292 (1963); Nakanishi K., Tada M., Yamada Y., Chem. Pharm. Bull., 12, 856-857 (1964); Nakanishi K., Ohashi M., Tada M., Yamada Y., Tetrahedron, 21, 1231-1246 (1965); Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M., Chem. Pharm. Bull., 12, 853-855 (1964).
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    • Nakanishi K., Ohashi M., Suzuki N., Tada M., Yamada Y , Inagaki S., Yakugaku Zasshi, 83, 377-380 (1963); Nakanishi K., Tada M., Yamada Y., Ohashi M., Komatsu N., Terakawa H., Nature (London), 197, 292 (1963); Nakanishi K., Tada M., Yamada Y., Chem. Pharm. Bull., 12, 856-857 (1964); Nakanishi K., Ohashi M., Tada M., Yamada Y., Tetrahedron, 21, 1231-1246 (1965); Tada M., Yamada Y., Bhacca N. S., Nakanishi K., Ohashi M., Chem. Pharm. Bull., 12, 853-855 (1964).
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.