Indole: A Privileged Heterocyclic Moiety in the Management of Cancer

Author:

Mir Reyaz Hassan1ORCID,Mohi-ud-din Roohi2ORCID,Wani Taha Umair3ORCID,Dar Mohammad Ovais4ORCID,Shah Abdul Jaleel1ORCID,Lone Bashir5ORCID,Pooja Chawla6ORCID,Masoodi Mubashir Hussain1ORCID

Affiliation:

1. Pharmaceutical Chemistry Division, Department of Pharmaceutical Sciences, University of Kashmir, Hazratbal, Srinagar-190006, Kashmir, India

2. Pharmacognosy Division, Department of Pharmaceutical Sciences, University of Kashmir, Hazratbal, Srinagar, 190006, Kashmir, India

3. Pharmaceutics Lab, Department of Pharmaceutical Sciences, School of Applied Sciences and Technology, University of Kashmir, Hazratbal, Srinagar-190006, Kashmir, India

4. Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), S.A.S. Nagar, Mohali, Punjab, 160062, India

5. Natural Product Chemistry Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu-180001, India

6. Department of Pharmaceutical Analysis, ISF College of Pharmacy, Moga-142001, India

Abstract

Heterocyclic are a class of compounds that are intricately entwined into life processes. Almost more than 90% of marketed drugs carry heterocycles. Synthetic chemistry, in turn, allocates a cornucopia of heterocycles. Among the heterocycles, indole, a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered pyrrole ring with numerous pharmacophores that generate a library of various lead molecules. Due to its profound pharmacological profile, indole got wider attention around the globe to explore it fully in the interest of mankind. The current review covers recent advancements on indole in the design of various anti-cancer agents acting by targeting various enzymes or receptors, including (HDACs), sirtuins, PIM kinases, DNA topoisomerases, and σ receptors.

Publisher

Bentham Science Publishers Ltd.

Subject

Organic Chemistry

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