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11-Deoxy-prostaglandin analogues - useful for treating e.g. asthma, more stable and selective and longer lasting than natural cpds.

机译:11-脱氧前列腺素类似物-用于治疗例如哮喘比天然cpds更稳定,更选择性,更持久。

摘要

Prostaglandins of formula (I) and their pharmaceutically acceptable salts with bases when R1 = H, are new. In the formula R1 = H or alkyl. R2 + R3 are together oxo or -SCH2CH2S or one is H and the other is OH. R4 = H or alkyl. R5 and R6 are each H or alkyl. R7 = H or alkyl. n = 3-6. m = 0-8, and A = CN, COOH, alkoxycarbonyl, N-disubstd. carbamoyl, OH or acyloxy. (I) are made e.g. by reacting a substd. 3-formylcyclopentanone with a Wittig reagent contg. -CO.CR5R6(CH2)mCHR7A (A protected where necessary) then reducing the oxo gps. Used esp. for treating asthma; excessive gastric secretion; as antihypertensives; to induce labour; as contraceptives; to synchronise oestrus (in veterinary medicine) and to treat arteriosclerosis. Compared with natural PG's they are more stable, more selective (fewer side effects) and have a longer lastic action.
机译:当R1 = H时,式(I)的前列腺素及其与碱的可药用盐是新的。式中,R 1 = H或烷基。 R 2 + R 3一起是氧代或-SCH 2 CH 2 S,或一个是H,另一个是OH。 R 4 = H或烷基。 R 5和R 6各自为H或烷基。 R 7 = H或烷基。 n = 3-6。 m = 0-8,且A = CN,COOH,烷氧羰基,N-二取代。氨基甲酰基,OH或酰氧基。 (I)例如通过反应。 3-甲酰基环戊酮与维蒂希试剂续。 -CO.CR5R6(CH2)mCHR7A(必要时受保护),然后降低氧代gps。二手的用于治疗哮喘;胃分泌过多;作为降压药;引诱劳工;作为避孕药;同步发情(兽药)和治疗动脉硬化。与天然PG相比,它们更稳定,更具选择性(副作用更少)且具有更长的弹力作用。

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