首页> 外国专利> 5-FLUOROURACIL DERIVATIVE, INHIBITOR OF BLOOD PLATELET AGGREGATION USING IT, AND PREVENTIVE FOR CANCER METASTASIS USING IT

5-FLUOROURACIL DERIVATIVE, INHIBITOR OF BLOOD PLATELET AGGREGATION USING IT, AND PREVENTIVE FOR CANCER METASTASIS USING IT

机译:5-氟尿嘧啶衍生物,使用它可抑制血小板凝集,并使用它可预防癌症的转移

摘要

NEW MATERIAL:A 5-fluorouracil derivative shown by the formula (R is acyl group derived from higher fatty acid of hexaene). EXAMPLE:1-(4,7,10,13,16,19-decosahexenoyl)-5-fluorouracil. USE:An inhibitor of blood platelet aggregation, preventive for cancer metastasis, or carcinostatic agent. A dose is 0.1-5g/adult/day, being administered orally, or by venoclysis or by hypodermic injection optionally 1-3 times, dividedly. PREPARATION:For example, a higher fatty acid of hexaene, preferably higher fatty acid having 22-24C is reacted with 5-fluorouracil in the presence of a condensation agent such as 2-chloro-1-methylpyridinium p-toluenesulfonate, etc. to give a compound shown by the formula.
机译:新材料:由式(R为衍生自己烯的高级脂肪酸的酰基)表示的5-氟尿嘧啶衍生物。实施例:1-(4,7,10,13,16,19-癸二十碳六烯酰基)-5-氟尿嘧啶。用途:血小板聚集抑制剂,可预防癌症转移或制癌剂。剂量为0.1-5g /成人/天,经口服,静脉溶毒或皮下注射任选地1-3次给药。制备:例如,在缩合剂例如2-氯-1-甲基吡啶对甲苯磺酸盐等存在下,使己烯的高级脂肪酸,优选具有22-24℃的高级脂肪酸与5-氟尿嘧啶反应,得到式所示的化合物。

著录项

  • 公开/公告号JPS59204175A

    专利类型

  • 公开/公告日1984-11-19

    原文格式PDF

  • 申请/专利权人 TERUMO KK;

    申请/专利号JP19830075427

  • 申请日1983-04-28

  • 分类号C07D239/553;A61K31/505;A61P7/02;A61P35/00;C07D239/54;

  • 国家 JP

  • 入库时间 2022-08-22 08:28:27

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