Medicinal chemistry of indole derivatives: Current to future therapeutic prospectives

被引:442
作者
Kumari, Archana [1 ,3 ]
Singh, Rajesh K. [2 ]
机构
[1] Rayat Bahra Inst Pharm, Sahauran 146104, Punjab, India
[2] Shivalik Coll Pharm, Dept Pharmaceut Chem, Maujowal 140126, Punjab, India
[3] IK Gujral Punjab Tech Univ, Fac Pharm, Jalandhar, Punjab, India
关键词
Indole nucleus; Synthesis; Medicinal Chemistry; Structure-activity relationship; Pharmacological profile; CELL LUNG-CANCER; NS5B POLYMERASE INHIBITOR; BIOLOGICAL EVALUATION; HEPATITIS-C; IN-VITRO; SELECTIVE INHIBITOR; PROTEIN-KINASE; ANTIMICROBIAL ACTIVITY; ANTIOXIDANT ACTIVITY; ANTIFUNGAL ACTIVITY;
D O I
10.1016/j.bioorg.2019.103021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Indole is a versatile pharmacophore, a privileged scaffold and an outstanding heterocyclic compound with wide ranges of pharmacological activities due to different mechanisms of action. It is an superlative moiety in drug discovery with the sole property of resembling different structures of the protein. Plenty of research has been taking place in recent years to synthesize and explore the various therapeutic prospectives of this moiety. This review summarizes some of the recent effective chemical synthesis (2014-2018) for indole ring. This review also emphasized on the structure-activity relationship (SAR) to reveal the active pharmacophores of various indole analogues accountable for anticancer, anticonvulsant, antimicrobial, antitubercular, antimalarial, antiviral, antidiabetic and other miscellaneous activities which have been investigated in the last five years. The precise features with motives and framework of each research topic is introduced for helping the medicinal chemists to understand the perspective of the context in a better way. This review will definitely offer the platform for researchers to strategically design diverse novel indole derivatives having different promising pharmacological activities with reduced toxicity and side effects.
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页数:35
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