CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review-Reference-Cited by-同舟云学术

CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review

Published:2020 Issue:10 Volume:10 Page:5610-5635
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Rani Alisha¹²³⁴,Singh Gurjaspreet¹⁵⁶⁷⁴^ORCID,Singh Akshpreet¹⁵⁶⁷⁴,Maqbool Ubair¹²³⁴,Kaur Gurpreet¹⁸⁹⁴,Singh Jandeep¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Lovely Professional University

3. Phagwara–144411

4. India

5. Centre of Advanced Studies in Chemistry

6. Panjab University

7. Chandigarh–160014

8. Gujranwala Guru Nanak Khalsa College

9. Ludhiana–141001

Abstract

The review lays emphasis on the significance of 1,2,3-triazoles synthesized via CuAAC reaction having potential to act as anti-microbial, anti-cancer, anti-viral, anti-inflammatory, anti-tuberculosis, anti-diabetic, and anti-Alzheimer drugs.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RA/C9RA09510A

Reference126 articles.

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2. Medicinal attributes of 1,2,3-triazoles: Current developments

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4. The growing impact of click chemistry on drug discovery

5. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

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