5-Fluorouracil derivatives XXIII. Synthesis and antitumor activities of 1-carbamoyl-5-fluorouracils having aromatic ring

In order to get good antitumor agents especially better than 5‐fluorouracil, tegafur and l‐hexylcarbamoyl‐5‐fluorouracil (HCFU), fourty nine 1‐carbamoyl‐5‐fluorouracil having aromatic ring were synthesized from 5‐fluorouracil and isocyanates or mines. Antitumor activity was tested in the L1210 tumor...

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Veröffentlicht in:Chinese journal of chemistry 1998-03, Vol.16 (2), p.171-177
Hauptverfasser: Shoichiro, Ozaki, Xiang-Zheng, Kong, Yutaka, Watanabe, Tomonori, Hoshiko, Tomio, Ogasawara, Takao, Ueno, Uiroyuki, Furukawa, Masaaki, Iigo, Akio, Hoshi
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Sprache:eng
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Zusammenfassung:In order to get good antitumor agents especially better than 5‐fluorouracil, tegafur and l‐hexylcarbamoyl‐5‐fluorouracil (HCFU), fourty nine 1‐carbamoyl‐5‐fluorouracil having aromatic ring were synthesized from 5‐fluorouracil and isocyanates or mines. Antitumor activity was tested in the L1210 tumor system, and 5 compounds gave better value of therapeutic ratio than 5‐fluorouracil, tegafur, HCFU. 1‐(4‐Methoxybenzylcarbamoyl)‐5‐fluorouracil gave the best result.
ISSN:1001-604X
1614-7065
DOI:10.1002/cjoc.19980160210