HETEROARYL DERIVATIVES AS PARP INHIBITORS

Disclosed are compounds of formula (I), their tautomeric forms, stereoisomers, and pharmaceutically acceptable salts thereof, wherein ring Ar, ring B, R1-R5, X, Y, p, q, r, and s are as defined in thespecification, pharmaceutical compositions including a compound, tautomer, stereoisomer, or salt the...

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Main Authors KAMBOJ RAJENDER KUMAR, TILEKAR AJAY RAMCHANDRA, GUPTA NISHANT RAMNIWASJI, PALLE VENKATA P, SINHA NEELIMA, KURHADE SANJAY PRALHAD, KARCHE NAVNATH POPAT, JADHAV GANESH RAJARAM
Format Patent
LanguageChinese
English
Published 17.04.2018
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Summary:Disclosed are compounds of formula (I), their tautomeric forms, stereoisomers, and pharmaceutically acceptable salts thereof, wherein ring Ar, ring B, R1-R5, X, Y, p, q, r, and s are as defined in thespecification, pharmaceutical compositions including a compound, tautomer, stereoisomer, or salt thereof, and methods of treating or preventing diseases or disorders, for example, cancer, that are amenable to treatment or prevention by inhibiting the PARP enzyme of a subject. 本发明公开了式(I)化合物、其互变异构形式、其立体异构体或其药学上可接受的盐,其中,环Ar、环B、R-R、X、Y、p、q、r和s如说明书中所定义;还公开了包括上述化合物互变异构形式、其立体异构体或其药学上可接受的盐的药物组合物,还公开了治疗或预防疾病或失调,例如癌症的方法,可通过抑制试验对象中PARP酶来治疗或预防。
Bibliography:Application Number: CN201680047044