Literature DB >> 30502116

An insight into medicinal chemistry of anticancer quinoxalines.

Tanu Kaushal1, Gaurava Srivastava1, Ashok Sharma2, Arvind Singh Negi3.   

Abstract

Quinoxalines are benzopyrazines containing benzene and pyrazine rings fused together. In the recent past, quinoxalines have attracted Medicinal Chemists considerably for their syntheses and chemistry due to their distinct pharmacological activities. Diverse synthetic protocols have been developed via multicomponent reactions, single pot synthesis and combinatorial approach using efficient catalysts, reagents, and nano-composites etc. Further, the versatility of the quinoxaline core and its reasonable chemical simplicity devise it extremely promising source of bioactive compounds. Therefore, a wide variety of bioactive quinoxalines has been realised as antitumour, antifungal, anti-inflammatory, antimicrobial, and antiviral agents. Already, a few of them are clinical drugs while many more are under various phases of clinical trials. Present review focuses on chemistry and pharmacology (both efficacy and safety) of quinoxalines and also provides some insight in to their structure-activity relationship.
Copyright © 2018. Published by Elsevier Ltd.

Entities:  

Keywords:  Anticancer; Pharmacokinetics; Quinoxalines; Structure activity relationship; Toxicity

Mesh:

Substances:

Year:  2018        PMID: 30502116     DOI: 10.1016/j.bmc.2018.11.021

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  9 in total

1.  Activities of Quinoxaline, Nitroquinoxaline, and [1,2,4]Triazolo[4,3-a]quinoxaline Analogs of MMV007204 against Schistosoma mansoni.

Authors:  Stefan L Debbert; Mikaela J Hintz; Christian J Bell; Kenya R Earl; Grant E Forsythe; Cécile Häberli; Jennifer Keiser
Journal:  Antimicrob Agents Chemother       Date:  2021-02-17       Impact factor: 5.191

2.  Green Hydrothermal Synthesis of Fluorescent 2,3-Diarylquinoxalines and Large-Scale Computational Comparison to Existing Alternatives.

Authors:  Fabián Amaya-García; Michael Caldera; Anna Koren; Stefan Kubicek; Jörg Menche; Miriam M Unterlass
Journal:  ChemSusChem       Date:  2021-03-26       Impact factor: 8.928

Review 3.  Recent advances in the transition-metal-free synthesis of quinoxalines.

Authors:  Biplob Borah; L Raju Chowhan
Journal:  RSC Adv       Date:  2021-11-19       Impact factor: 4.036

Review 4.  Ultrasound-assisted transition-metal-free catalysis: a sustainable route towards the synthesis of bioactive heterocycles.

Authors:  Biplob Borah; L Raju Chowhan
Journal:  RSC Adv       Date:  2022-05-11       Impact factor: 4.036

5.  Tin(ii) chloride dihydrate/choline chloride deep eutectic solvent: redox properties in the fast synthesis of N-arylacetamides and indolo(pyrrolo)[1,2-a]quinoxalines.

Authors:  Sergio Alfonso Trujillo; Diana Peña-Solórzano; Oscar Rodríguez Bejarano; Cristian Ochoa-Puentes
Journal:  RSC Adv       Date:  2020-11-06       Impact factor: 3.361

6.  A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines.

Authors:  Alexander V Aksenov; Nikolai A Arutiunov; Dmitrii A Aksenov; Artem V Samovolov; Igor A Kurenkov; Nicolai A Aksenov; Elena A Aleksandrova; Daria S Momotova; Michael Rubin
Journal:  Int J Mol Sci       Date:  2022-09-22       Impact factor: 6.208

7.  Synthesis, DNA-Binding, Anticancer Evaluation, and Molecular Docking Studies of Bishomoleptic and Trisheteroleptic Ru-Diimine Complexes Bearing 2-(2-Pyridyl)-quinoxaline.

Authors:  Sofia Balou; Athanasios Zarkadoulas; Maria Koukouvitaki; Luciano Marchiò; Eleni K Efthimiadou; Christiana A Mitsopoulou
Journal:  Bioinorg Chem Appl       Date:  2021-05-12       Impact factor: 7.778

8.  Structure activity relationship (SAR) study identifies a quinoxaline urea analog that modulates IKKβ phosphorylation for pancreatic cancer therapy.

Authors:  Satish Sagar; Sarbjit Singh; Jayapal Reddy Mallareddy; Yogesh A Sonawane; John V Napoleon; Sandeep Rana; Jacob I Contreras; Christabelle Rajesh; Edward L Ezell; Smitha Kizhake; Jered C Garrison; Prakash Radhakrishnan; Amarnath Natarajan
Journal:  Eur J Med Chem       Date:  2021-05-30       Impact factor: 7.088

Review 9.  Microwave Assisted Reactions of Azaheterocycles Formedicinal Chemistry Applications.

Authors:  Dorina Amariucai-Mantu; Violeta Mangalagiu; Ramona Danac; Ionel I Mangalagiu
Journal:  Molecules       Date:  2020-02-07       Impact factor: 4.411

  9 in total

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