Indazole scaffold: a generalist for marketed and clinical drugs

被引:33
作者
Cao, Yaquan [1 ,2 ,3 ,4 ]
Luo, Chunying [1 ,2 ,3 ,4 ]
Yang, Pu [1 ,2 ,3 ,4 ]
Li, Pan [1 ,2 ,3 ,4 ]
Wu, Chunli [1 ,2 ,3 ,4 ]
机构
[1] Zhengzhou Univ, Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[2] Key Lab Adv Drug Preparat Technol, Mil Educ, Zhengzhou 450001, Peoples R China
[3] Sch Pharmaceut Sci, Zhengzhou 450001, Peoples R China
[4] Zhengzhou Key Lab New Vet Drug Preparat Innovat, Zhengzhou 450001, Peoples R China
关键词
Indazole; Clinical; Drug; Disease; Pharmacology activity; PHASE-II TRIAL; TYROSINE KINASE INHIBITOR; CHEMOTHERAPY-INDUCED NAUSEA; METASTATIC BREAST-CANCER; CHRONIC LYMPHOCYTIC-LEUKEMIA; CELL LUNG-CANCER; DUP-937; TELOXANTRONE; ANTITUMOR-ACTIVITY; MALIGNANT-MELANOMA; ANTICANCER-DRUG;
D O I
10.1007/s00044-020-02665-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
More and more attention has been paid to the structurally diverse indazole analogs in recent years which are widely present in numerous commercially available drugs. Indazole-containing derivatives are endowed with a broad range of biological properties, such as anti-inflammatory, antibacterial, anti-HIV, antiarrhythmics, antifungal and antitumor activities. This review is a guide for pharmacologists who are in search of valid preclinical/clinical drug compounds where the progress, from 1966 to the present day, of approved marketed drugs containing indazole scaffold is examined.
引用
收藏
页码:501 / 518
页数:18
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