首页> 外国专利> New 4-(omega-arylalkyl)phenylalkanoic acid derivs. - used as LTB4 inhibitors for treating eczema, psoriasis, acne, arthritis, asthma, allergies or inflammatory bowel disease

New 4-(omega-arylalkyl)phenylalkanoic acid derivs. - used as LTB4 inhibitors for treating eczema, psoriasis, acne, arthritis, asthma, allergies or inflammatory bowel disease

机译:衍生出新的4-(ω-芳基烷基)苯基链烷酸。 -用作LTB4抑制剂,用于治疗湿疹,牛皮癣,痤疮,关节炎,哮喘,过敏或炎症性肠病

摘要

Phenylalkanoic acids, their salts and/or derivs. of formula (I) are new. In (I), R1 is pyridyl, quinolyl, naphthyl or R6R7-phenyl; R6 and R7 are H, halo, Me, OH, trihalomethyl (esp. CF3), NO2, NH2 (opt. substd. by alkyl, esp. 1 or 2 Me), phenyl, tert. butyl, -NR9-COR5 or -NH-SO2R8; R8 is phenyl, Me or trihalomethyl (esp. CF3); R9 is H or Me; R2 is bond, CO, CH2, or CHOH; R3 is bond, CO, S, O, SO2, HOCO or CH2; R4 is bond, OCH2 or -CR10R11-; R10 and R11 are H and/or Me; R5 is H, alkyl, (esp. Me or Et), or alkali metal (esp. Na or K); m is 0-3; n is 4-7. (I) are derived from pentanoic, hexanoic, heptanoic or octanoic acids, or their Me or Et esters. (I) may be prepd. by reacting acid chloride of formula (1) R-(CH2)m-CoCl with aryl alkyl ester of formula (ii) where R13 is R3 other than CO or SO2; R15 is alkyl). Reaction is under usual conditions for Friedel-crafts acylation and the ester prods. can be hydrolysed conventionally. USE/ADVANTAGE - (I) are inhibitors of leucotriene-A4 hydrolysis so are useful for treatment of chronic inflammation esp. rheumatic diseases (esp. arthritis), psoriasis, eczema, acne and other skin conditions; intestinal inflammatory lesions; allergy and asthma. They are administered orally, rectally or parenterally, pref. in unit doses of 10-150 mg.
机译:苯基链烷酸,其盐和/或衍生物。式(I)的化学式是新的。在(I)中,R 1为吡啶基,喹啉基,萘基或R 6 R 7-苯基; R 6和R 7是H,卤素,Me,OH,三卤甲基(特别是CF 3),NO 2,NH 2(优选被烷基取代,特别是1或2 Me),苯基,叔。丁基,-NR9-COR5或-NH-SO2R8; R8是苯基,Me或三卤甲基(尤其是CF3); R9是H或Me; R2是键,CO,CH2或CHOH; R3是键,CO,S,O,SO2,HOCO或CH2; R4是键,OCH2或-CR10R11-; R10和R11是H和/或Me; R 5是H,烷基(尤其是Me或Et)或碱金属(特别是Na或K); m为0-3; n为4-7。 (I)衍生自戊酸,己酸,庚酸或辛酸,或它们的Me或Et酯。 (I)可以准备。通过使式(1)的酰氯与R-(CH2)m-CoCl与式(ii)的芳烷基酯反应,其中R13为CO或SO2以外的R3; R 15是烷基。反应是在通常条件下进行的,用于Friedel-crafts酰化和酯产物。可以常规水解。用途/优点-(I)是白三烯A4水解的抑制剂,因此可用于治疗慢性炎症,尤其是。风湿性疾病(尤其是关节炎),牛皮癣,湿疹,粉刺和其他皮肤疾病;肠炎性病变;过敏和哮喘。它们优选口服,直肠或肠胃外给药。以10-150 mg的单位剂量服用。

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