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application of pteridinforbindelser for prevention of primary and secondary resistance to chemotherapy, and medicinal products containing these compounds

机译:蝶呤/ bindelser在预防对化疗的原发性和继发性耐药中的应用,以及含有这些化合物的药物

摘要

The invention relates to medicaments containing a pteridine of the formula IMAGE in which n is the number 0 or 1, R2 and R7 are each a pyrrolidino, piperidino or morpholino group which is optionally substituted by one or two methyl groups, R3 is a straight-chain or branched alkyl group in which one or two carbon atoms, excepting the carbon atom adjacent to the nitrogen atom, can be substituted by a hydroxyl group, R4 is an alkyl or phenylalkyl group, in which one carbon atom, excepting the carbon atom adjacent to the nitrogen atom, can be substituted by a hydroxyl group, and R5 is a hydrogen atom or a methyl group, or the acid addition salts thereof and at least one chemotherapeutic from the natural product series, and to the use of the above pteridines for sensitisation of tumours during chemotherapy with the abovementioned chemotherapeutics, and to pteridines, process for the preparation thereof and medicaments containing these pteridines.
机译:本发明涉及包含式的蝶啶的药物,其中n为0或1,R 2和R 7各自为吡咯烷基,哌啶子基或吗啉代基团,其任选地被一个或两个甲基取代,R 3为A。直链或支链烷基,其中除与氮原子相邻的碳原子外,一个或两个碳原子可被羟基取代,R 4为烷基或苯基烷基,其中一个碳原子, R 5为氢原子或甲基,或其酸加成盐和至少一种来自天然产物系列的化学疗法,除与氮原子相邻的碳原子外,可被羟基取代,R 5为氢原子或甲基,及其用途用于在使用上述化学疗法的化疗过程中致敏肿瘤的上述蝶啶,及其对蝶啶的制备方法和含有这些蝶啶的药物。

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