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5-Alkyl:pyridazinyl substd. benzimidazole derivs. - useful as cardiovascular agents, antivirals, interferon inducers and ulcer inhibitors

机译:5-烷基:哒嗪基。苯并咪唑衍生物。 -可用作心血管药物,抗病毒药,干扰素诱导剂和溃疡抑制剂

摘要

Benzimidazole derivs. of formula (I) and their optical antipodes when A = B = H, and their physiologically acceptable salts with organic or inorganic acids are new: (A and B are each H, or together make a double bond; R1 = H, CF3, 1-11C alkyl, 3-7C cycloalkyl, OH or SH (both opt. etherified with 1-6C alkyl), phenyl (1-3C) alkyl, or phenyl (opt. substd. by 1-3 same or different halo, 1-4C alkyl, 1-6C alkylsulphinyl, OH or SH, both the latter opt. etherified with 1-6C alkyl); R2 = H, 1-5C alkyl, 3-6C cycloalkyl or phenyl (1-3C) alkyl; R3 = 1-6C alkyl). (I) have antiviral, interferon-inducing, ulcer-inhibiting and esp. cardiovascular (cardiotonic, hypotensive and/or antithrombotic) activities.
机译:苯并咪唑衍生。式(I)及其光学对映体的化学式(A = B = H,以及它们与有机或无机酸的生理可接受盐)是新的:(A和B各自为H,或一起形成双键; R1 = H,CF3, 1-11C烷基,3-7C环烷基,OH或SH(均用1-6C烷基醚化),苯基(1-3C)烷基或苯基(均用1-3个相同或不同的卤素取代,1 -4C烷基,1-6C烷基亚磺酰基,OH或SH,后者均用1-6C烷基醚化; R2 = H,1-5C烷基,3-6C环烷基或苯基(1-3C)烷基; R3 = 1-6C烷基)。 (I)具有抗病毒,诱导干扰素,抑制溃疡和抑制作用。心血管(强心,降压和/或抗血栓形成)活动。

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