The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, pulmonary fibrosis, hepatic fibrosis, glomerulonephritis, and other renal disorders, and for the treatment of viral infections (both acute and chronic).
The invention generally relates to the field of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to new substituted-heterocyclic azole compounds, the synthesis and use of these compounds and their pharmaceutical compositions, e.g., in the treatment, modulation and/or prevention of physiological conditions associated with CRM1 activity such as in treating cancer and other neoplastic disorders, inflammatory diseases, disorders of abnormal tissue growth and fibrosis including cardiomyopathy, pulmonary fibrosis, hepatic fibrosis, glomerulonephritis, and other renal disorders, and for the treatment of viral infections (both acute and chronic).
Methods of promoting wound healing using CRM1 inhibitors
申请人:Karyopharm Therapeutics Inc.
公开号:US10202366B2
公开(公告)日:2019-02-12
The invention generally relates to the use of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to a compound represented by structural formula I:
or a pharmaceutically acceptable salt thereof, wherein Ring A, X, R1, R2 and n are as defined and described herein, in a method for promoting wound healing in a subject.
本发明一般涉及核转运调节剂(如 CRM1 抑制剂)的使用,特别是结构式 I 所代表的化合物:
或其药学上可接受的盐,其中环 A、X、R1、R2 和 n 如本文所定义和描述,用于促进受试者伤口愈合的方法。
Methods of Promoting Wound Healing Using CRM1 Inhibitors
申请人:KARYOPHARM THERAPEUTICS INC.
公开号:US20160304500A1
公开(公告)日:2016-10-20
The invention generally relates to the use of nuclear transport modulators, e.g., CRM1 inhibitors, and more particularly to a compound represented by structural formula (I) or a pharmaceutically acceptable salt thereof, wherein Ring A, X, R
1
, R
2
and n are as defined and described herein, in a method for promoting wound healing in a subject.