Literature DB >> 27543880

Oxindole: A chemical prism carrying plethora of therapeutic benefits.

Maninder Kaur1, Manjinder Singh1, Navriti Chadha1, Om Silakari2.   

Abstract

Oxindole has emerged as a valuable scaffold in medicinal chemistry possessing diverse range of pharmacological activities. Its value has further been increased by its natural occurrence as alkaloids in variety of plants. It was first extracted from the cat claw's plant Uncaria tomentosa found in the Amazon rainforest and other tropical areas of South and Central America. Traditionally as well as present emerging therapeutic potential of oxindole nucleus has captured the interest of medicinal chemists to synthesize novel oxindole derivatives. In the present review the authors have integrated its chemistry and synthetic strategies developed after 1945. Also the information of naturally occurring oxindole alkaloids has been incorporated. The detailed pharmacological activities including anti-cancer, anti-HIV, antidiabetic, antibacterial, antioxidant, kinase inhibitory, AChE inhibitory, anti-leishmanial, β3 adrenergic receptor agonistic, phosphatase inhibitory, analgesic, spermicidal, vasopressin antagonists, progesterone antagonists, neuroprotection, and NMDA blocker activities of oxindole derivatives alongwith their SAR has also been discussed in detail. Additionally, information regarding the oxindole derivatives in clinical trials has been incorporated. Thus, this review will provide insights for the synthetic as well as medicinal chemist for the designing and synthesis of novel oxindole derivatives with novel improved range of pharmacological implications.
Copyright © 2016 Elsevier Masson SAS. All rights reserved.

Entities:  

Keywords:  Anti-cancer; Anti-oxidant; Kinase inhibitory activity; Oxindole; Sunitinib

Mesh:

Substances:

Year:  2016        PMID: 27543880     DOI: 10.1016/j.ejmech.2016.08.011

Source DB:  PubMed          Journal:  Eur J Med Chem        ISSN: 0223-5234            Impact factor:   6.514


  21 in total

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3.  Ruthenium(0)-Catalyzed C-C Coupling of Alkynes and 3-Hydroxy-2-oxindoles: Direct C-H Vinylation of Alcohols.

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4.  Palladium-Catalyzed Reductive Heck Coupling of Alkenes.

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Journal:  Trends Chem       Date:  2019-06-20

5.  Macrocyclic Modalities Combining Peptide Epitopes and Natural Product Fragments.

Authors:  Stéphanie M Guéret; Sasikala Thavam; Rodrigo J Carbajo; Marco Potowski; Niklas Larsson; Göran Dahl; Anita Dellsén; Tom N Grossmann; Alleyn T Plowright; Eric Valeur; Malin Lemurell; Herbert Waldmann
Journal:  J Am Chem Soc       Date:  2020-03-02       Impact factor: 15.419

Review 6.  Recent Advances in Asymmetric Organocatalyzed Conjugate Additions to Nitroalkenes.

Authors:  Diego A Alonso; Alejandro Baeza; Rafael Chinchilla; Cecilia Gómez; Gabriela Guillena; Isidro M Pastor; Diego J Ramón
Journal:  Molecules       Date:  2017-05-29       Impact factor: 4.411

7.  Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles with Alcohols.

Authors:  Mubarak B Dambatta; Kurt Polidano; Alexander D Northey; Jonathan M J Williams; Louis C Morrill
Journal:  ChemSusChem       Date:  2019-05-07       Impact factor: 8.928

8.  Three-component three-bond forming cascade via palladium photoredox catalysis.

Authors:  Peter Bellotti; Maximilian Koy; Christian Gutheil; Steffen Heuvel; Frank Glorius
Journal:  Chem Sci       Date:  2020-12-07       Impact factor: 9.825

9.  Enantioselective catalytic β-amination through proton-coupled electron transfer followed by stereocontrolled radical-radical coupling.

Authors:  Zijun Zhou; Yanjun Li; Bowen Han; Lei Gong; Eric Meggers
Journal:  Chem Sci       Date:  2017-06-15       Impact factor: 9.825

10.  Synthesis of 2-Mercapto-(2-Oxoindolin-3-Ylidene)Acetonitriles from 3-(4-Chloro-5H-1,2,3-Dithiazol-5-Ylidene)Indolin-2-ones.

Authors:  Boris Letribot; Régis Delatouche; Hervé Rouillard; Antoine Bonnet; Jean-René Chérouvrier; Lisianne Domon; Thierry Besson; Valérie Thiéry
Journal:  Molecules       Date:  2018-06-08       Impact factor: 4.411

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