Combretoxazolones : synthesis, cytotoxicity and antitumor activity

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dc.contributor.authorNguyen-Hai Nam-
dc.contributor.authorYong Kim-
dc.contributor.authorYoung Jae You-
dc.contributor.authorDong Ho Hong-
dc.contributor.authorHwan Mook Kim-
dc.contributor.authorByung Zun Ahn-
dc.date.accessioned2017-04-19T08:58:29Z-
dc.date.available2017-04-19T08:58:29Z-
dc.date.issued2001-
dc.identifier.issn0960-894X-
dc.identifier.uri10.1016/S0960-894X(01)00622-9ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/5622-
dc.description.abstractTwo series of combretoxazolones including 3,4-diaryloxazolones (6) and 4,5-diaryloxazolones (7) were synthesized and evaluated for cytotoxicity and antitumor activity. Both series showed strong cytotoxicities against a variety of tumor cell lines. Compound 6g exhibited a significant antitumor activity in BDF1 mice bearing B16 murine melanoma cells with inhibition rates of 67 and 61% at 100 and 30 mg/kg/day, respectively.-
dc.publisherElsevier-
dc.titleCombretoxazolones : synthesis, cytotoxicity and antitumor activity-
dc.title.alternativeCombretoxazolones : synthesis, cytotoxicity and antitumor activity-
dc.typeArticle-
dc.citation.titleBioorganic & Medicinal Chemistry Letters-
dc.citation.number23-
dc.citation.endPage3076-
dc.citation.startPage3073-
dc.citation.volume11-
dc.contributor.affiliatedAuthorDong Ho Hong-
dc.contributor.affiliatedAuthorHwan Mook Kim-
dc.contributor.alternativeNameNam-
dc.contributor.alternativeName김용-
dc.contributor.alternativeName유영재-
dc.contributor.alternativeName홍동호-
dc.contributor.alternativeName김환묵-
dc.contributor.alternativeName안병준-
dc.identifier.bibliographicCitationBioorganic & Medicinal Chemistry Letters, vol. 11, no. 23, pp. 3073-3076-
dc.identifier.doi10.1016/S0960-894X(01)00622-9-
dc.description.journalClassY-
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