Benzothiazole Congenres and It’s Therapeutic Consequence: Mini statement

Clicks: 1
ID: 309234
2024
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal

Ranked #135 of 153 articles by views in International Journal of Pharmaceutical Drug Design (IJPDD)

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 153 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Benzothiazole are important class of hetero compounds because it has unique and versatile scaffold for experimental design. In recent year heterocyclic compounds and their derivatives have wide range biological and pharmacological properties, Benzothiazole analogues are used in evaluating new product that possesses different biological activities. Hence their structural modification produces new derivatives causes wide range of biological and pharmacological activities such as antimicrobial, antiviral, anti-inflammatory, anti-consultant etc. This review summarises the various effect of substituent to develop new derivatives having good pharmacological properties. Benzothiazole is an organic compound bearing a heterocyclic nucleus (thiazole) which imparts a wide spectrum of biological activities to it. The significant and potent activity of benzothiazole moiety influenced distinctively by nature and position of substitutions. This review summarizes the effect of various substituents in recent trends and approaches to design and develop novel benzothiazole derivatives for anticancer potential in different cell lines by interpreting the Structure- Activity Relationship (SAR) and mechanism of action of a wide range of derivatives.
Reference Key
imported_1761926729_6904de4962e5f Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Triloki Prasad, Surjeet Singh, Priya Bharti, Shrutikant Gupta, Madhu Sharma, Priyanka Yadav, Deepak Kumar
Journal International Journal of Pharmaceutical Drug Design (IJPDD)
Year 2024
DOI
10.62896/ijpdd.1.6.3
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.