Literature DB >> 25458785

Quinoline: a promising antitubercular target.

Rangappa S Keri1, Siddappa A Patil2.   

Abstract

Tuberculosis (TB) remains a global public health problem in recent years. TB originated mainly from various strains of Mycobacterium tuberculosis, is a highly infectious and chronic disease with high infection rate since ancient times. Since the last 50 years, the same long-duration, multidrug treatment plan is being followed for the treatment of tuberculosis. Due to the development of resistance to conventional antibiotics there is a need for new therapeutic strategies to combat M. tuberculosis. Subsequently, there is an urgent need for the development of new drug molecules with newer targets and with an alternative mechanism of action. Among hetrocyclic compounds, quinoline compounds are important privileged structure in medicinal chemistry, are widely used as "parental" compounds to synthesize molecules with medical benefits, especially with anti-malarial and anti-microbial activities. Certain, quinoline-based compounds, also show effective anti-TB activity. This broad spectrum of biological and biochemical activities has been further facilitated by the synthetic versatility of quinoline, which allows the generation of a large number of structurally diverse derivatives. To pave the way for future research, there is a need to collect the latest information in this promising area. In the present review, we have collated published reports on this versatile core to provide an insight so that its full therapeutic potential can be utilized for the treatment tuberculosis. It is hoped that, this review will be helpful for new thoughts in the quest for rational designs of more active and less toxic quinoline-based anti-TB drugs.
Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Anti-tubercular; Medicinal chemistry; Mycobacterium tuberculosis; Quinoline; Synthesis; Tubercle Bacillus

Mesh:

Substances:

Year:  2014        PMID: 25458785     DOI: 10.1016/j.biopha.2014.10.007

Source DB:  PubMed          Journal:  Biomed Pharmacother        ISSN: 0753-3322            Impact factor:   6.529


  19 in total

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2.  The regioselective one-pot four-component synthesis of novel functionalized 4H-pyrano[2, 3-b]quinoline derivatives using DABCO as a homogeneous organocatalyst.

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Journal:  ACS Comb Sci       Date:  2017-10-27       Impact factor: 3.784

5.  Regioselective ring expansion followed by H-shift of 3-ylidene oxindoles: a convenient synthesis of N-substituted/un-substituted pyrrolo[2,3-c] quinolines and marinoquinolines.

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Journal:  RSC Adv       Date:  2019-10-30       Impact factor: 3.361

6.  Synthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamidesAQ3 as carbonic anhydrase isoforms I and II inhibitors.

Authors:  Mohammad M Al-Sanea; Ahmed Elkamhawy; Sora Paik; Silvia Bua; So Ha Lee; Mohamed A Abdelgawad; Eun Joo Roh; Wagdy M Eldehna; Claudiu T Supuran
Journal:  J Enzyme Inhib Med Chem       Date:  2019-12       Impact factor: 5.051

7.  Utilization of Water-Soluble Aminoethylamino-β-Cyclodextrin in the Pfitzinger Reaction-Catalyzed to the Synthesis of Diversely Functionalized Quinaldine.

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Journal:  Polymers (Basel)       Date:  2020-02-09       Impact factor: 4.329

8.  Synthesis of hexahydrofuro[3,2-c]quinoline, a martinelline type analogue and investigation of its biological activity.

Authors:  P-Y Chung; J C-O Tang; C-H Cheng; Z-X Bian; W-Y Wong; K-H Lam; C-H Chui
Journal:  Springerplus       Date:  2016-03-03

9.  One-Pot Multicomponent Synthesis and Bioevaluation of Tetrahydroquinoline Derivatives as Potential Antioxidants, α-Amylase Enzyme Inhibitors, Anti-Cancerous and Anti-Inflammatory Agents.

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Journal:  Molecules       Date:  2020-06-11       Impact factor: 4.411

10.  Quinolines derivatives as promising new antifungal candidates for the treatment of candidiasis and dermatophytosis.

Authors:  Gabriella da Rosa Monte Machado; Denise Diedrich; Thaís Carine Ruaro; Aline Rigon Zimmer; Mário Lettieri Teixeira; Luís Flávio de Oliveira; Mickael Jean; Pierre Van de Weghe; Saulo Fernandes de Andrade; Simone Cristina Baggio Gnoatto; Alexandre Meneghello Fuentefria
Journal:  Braz J Microbiol       Date:  2020-07-31       Impact factor: 2.476

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