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Substituted heterocyclic compounds as CRAC modulators
专利权人:
LUPIN LIMITED
发明人:
Nageswara Rao Irlapati,Nilesh Raghunath Khedkar,Ravindra Babanrao Jape,Rahul Shripad Nandurdikar,Zubair Abdul Wajid Shaikh,Neelima Sinha,Venkata P. Palle,Rajender Kumar Kamboj
申请号:
US14899719
公开号:
US09725463B2
申请日:
2014.06.20
申请国别(地区):
US
年份:
2017
代理人:
摘要:
The invention relates to compounds of Formula (I) and their pharmaceutically acceptable salts, wherein the substituents are as described herein, and their use in medicine for the treatment of diseases, disorders associated with the modulation of calcium release-activated calcium (CRAC) channel. The invention also relates to pharmaceutical compositions containing such compounds in treating diseases disorders associated with calcium release-activated calcium (CRAC) channel modulators. wherein, ring D is Formula (a) or Formula (b): A and B, which may be same or different, are independently CR3 or N; Y is CR3 or N; L is selected from —NR2C(O)—, —C(O)NR2— and —NR2CRaRb—; Ra and Rb are independently hydrogen, halogen or substituted or unsubstituted alkyl; ring E is selected from the Formula (i) to (vii).
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