FIELD: organic chemistry, pharmacy. SUBSTANCE: invention describes the novel derivatives of 1,5-benzodiazepine of the general formula (I) and their pharmaceutically acceptable salts where R1 - phenyl or C1-6-alkyl group being indicated alkyl group can be substituted with C3-7-cycloalkyl or C7-11-cycloalkyl (bridge) group; R2 means phenyl group possibly substituted with substituents taken from the following ones: halogen atom, C1-4-alkyl, trifluoromethyl or (CH2)nR4 where R4 means hydroxy- or C1-4-alkoxy-group and n = 0; R3 means a group AlkN-R8R9 where ALk is a direct C2-6-alkylene chain possibly substituted with hydroxyl group; R8 and R9 in common with nitrogen atom to which they bound form 5-7-membered saturated heterocyclic ring possibly containing an additional heteroatom taken from the following ones: oxygen or nitrogen atom; R10 means halogen atom; X means NH residue; m = 0 or 1. The above indicated compounds are antagonists of gastrin and cholecystokinin. EFFECT: new compounds indicated above, valuable pharmacological properties. 12 cl, 18 ex
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Authors
Dates
1999-08-27—Published
1994-07-18—Filed