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USE OF LIGANDS FROM THE PERIPHERAL BINDING SITES FOR BENZODIAZEPINES FOR THE PREPARATION OF DRUGS USEFUL IN THE TREATMENT OF PERIPHERAL NEUROPATHIES
USE OF LIGANDS FROM THE PERIPHERAL BINDING SITES FOR BENZODIAZEPINES FOR THE PREPARATION OF DRUGS USEFUL IN THE TREATMENT OF PERIPHERAL NEUROPATHIES
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机译:苯二氮卓类药物在外周结合部位的药物在制备治疗周围神经病中有用的药物的使用
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摘要
The use of ligands for the peripheral bonding sites of benzodiazepines (p-sites) in the preparation of medicaments for the prevention and treatment of peripheral neuropathies is new. The preferred p-site ligands are of formula (I). X = H, halo, 1-4C alkyl, 1-4C alkoxy, CF3, CH3S, NO2, or NH2; Y1 = H, halo or 1-4C alkyl; Y2 = OH, 1-4C alkoxy, or SR; R = H, 1-4C alkyl, or (4-alkoxyphenyl)methyl; R1, R2 = H or 1-4C alkyl.
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机译:在制备用于预防和治疗周围神经病的药物中,将配体用于苯并二氮杂卓的外围结合位点(p位)是新的。优选的对位配体为式(I)。 X = H,卤素,1-4C烷基,1-4C烷氧基,CF3,CH3S,NO2或NH2; Y 1 = H,卤素或1-4C烷基; Y 2 = OH,1-4C烷氧基或SR; R = H,1-4C烷基或(4-烷氧基苯基)甲基; R1,R2 = H或1-4C烷基。
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