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作為組蛋白去乙酰酶6抑制劑的1,3,4-噁二唑磺酰胺衍生物及含其的醫藥組合物
专利权人:
CHONG KUN DANG PHARMACEUTICAL CORP.;株式會社鐘根堂
发明人:
LEE, Jaekwang,HAN, Younghue,KIM, Yuntae,MIN, Jaeki,BAE, Miseon,KIM, Dohoon,JIN, Seokmin,KYUNG, Jangbeen,BAE, Miseon,裴美善,KIM, Dohoon,金度勳,JIN, Seokmin,秦石珉,KYUNG, Jangbeen,慶奘䎙
申请号:
HK18110812
公开号:
HK1251549A1
申请日:
2018.08.22
申请国别(地区):
HK
年份:
2019
代理人:
摘要:
The present invention relates to novel compounds having histone deacetylase 6 (HDAC6) inhibitory activity, stereoisomers thereof or pharmaceutically acceptable salts thereof, the use thereof for the preparation of therapeutic medicaments, pharmaceutical compositions containing the same, a method for treating diseases using the composition, and methods for preparing the novel compounds. The novel compounds, stereoisomers thereof or pharmaceutically acceptable salts thereof according to the present invention have histone deacetylase (HDAC) inhibitory activity and are effective for the prevention or treatment of HDAC6-mediated diseases, including infectious diseases; neoplasms; endocrine, nutritional and metabolic diseases; mental and behavioral disorders; neurological diseases; diseases of the eye and adnexa; cardiovascular diseases; respiratory diseases; digestive diseases; diseases of the skin and subcutaneous tissue; diseases of the musculoskeletal system and connective tissue; or congenital malformations, deformations and chromosomal abnormalities.
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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