Literature DB >> 32106717

An overview of spirooxindole as a promising scaffold for novel drug discovery.

Li-Ming Zhou1, Ren-Yu Qu1, Guang-Fu Yang1.   

Abstract

Introduction: Spirooxindole, a unique and versatile scaffold, has been widely studied in some fields such as pharmaceutical chemistry and synthetic chemistry. Especially in the application of medicine, quite a few compounds featuring spirooxindole motif have displayed excellent and broad pharmacological activities. Many identified candidate molecules have been used in clinical trials, showing promising prospects.Areas covered: This article offers an overview of different applications and developments of spirooxindoles (including the related natural products and their derivatives) in the process of drug innovation, including such as in anticancer, antimicrobial, anti-inflammatory, analgesic, antioxidant, antimalarial, and antiviral activities. Furthermore, the crucial structure-activity relationships, molecular mechanisms, pharmacokinetic properties, and main synthetic methods of spirooxindoles-based derivatives are also reviewed.Expert opinion: Recent progress in the biological activity profiles of spirooxindole derivatives have demonstrated their significant position in present-day drug discovery. Furthermore, we believe that the multidirectional development of novel drugs containing this core scaffold will continue to be the research hotspot in medicinal chemistry in the future.

Entities:  

Keywords:  Spirooxindole; anticancer; antimicrobial; bioactivity; natural products; structure-activity relationship

Mesh:

Substances:

Year:  2020        PMID: 32106717     DOI: 10.1080/17460441.2020.1733526

Source DB:  PubMed          Journal:  Expert Opin Drug Discov        ISSN: 1746-0441            Impact factor:   6.098


  13 in total

Review 1.  Recent Strategies in the Synthesis of Spiroindole and Spirooxindole Scaffolds.

Authors:  Shima Nasri; Mohammad Bayat; Faezeh Mirzaei
Journal:  Top Curr Chem (Cham)       Date:  2021-05-18

Review 2.  1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments.

Authors:  Fatemeh Rostami Miankooshki; Mohammad Bayat; Shima Nasri; Narges Habibi Samet
Journal:  Mol Divers       Date:  2022-08-04       Impact factor: 3.364

3.  Design and synthesis of novel quinazolinyl-bisspirooxindoles as potent anti-tubercular agents: an ultrasound-promoted methodology.

Authors:  Bhargava Sai Allaka; Srinivas Basavoju; Estharla Madhu Rekha; Dharmarajan Sriram; Gamidi Rama Krishna
Journal:  Mol Divers       Date:  2022-08-06       Impact factor: 3.364

4.  Three-Component [3+2] Cycloaddition for Regio- and Diastereoselective Synthesis of Spirooxindole-Pyrrolidines.

Authors:  Xiaofeng Zhang; Miao Liu; Desheng Zhan; Manpreet Kaur; Jerry P Jasinski; Wei Zhang
Journal:  New J Chem       Date:  2022-01-20       Impact factor: 3.925

5.  Synthesis and Structure Elucidation of Novel Spirooxindole Linked to Ferrocene and Triazole Systems via [3 + 2] Cycloaddition Reaction.

Authors:  Mezna Saleh Altowyan; Saied M Soliman; Matti Haukka; Nora Hamad Al-Shaalan; Aminah A Alkharboush; Assem Barakat
Journal:  Molecules       Date:  2022-06-25       Impact factor: 4.927

Review 6.  Spirocyclic derivatives as antioxidants: a review.

Authors:  Karen Acosta-Quiroga; Cristian Rojas-Peña; Luz Stella Nerio; Margarita Gutiérrez; Efraín Polo-Cuadrado
Journal:  RSC Adv       Date:  2021-06-21       Impact factor: 4.036

7.  Synthesis of a New Class of Spirooxindole-Benzo[b]Thiophene-Based Molecules as Acetylcholinesterase Inhibitors.

Authors:  Assem Barakat; Saeed Alshahrani; Abdullah Mohammed Al-Majid; M Ali; Mezna Saleh Altowyan; Mohammad Shahidul Islam; Abdullah Saleh Alamary; Sajda Ashraf; Zaheer Ul-Haq
Journal:  Molecules       Date:  2020-10-13       Impact factor: 4.411

8.  Novel cellulose supported 1,2-bis(4-aminophenylthio)ethane Ni(ii) complex (NiII(BAPTE)(NO3)2-Cell) as an efficient nanocatalyst for the synthesis of spirooxindole derivatives.

Authors:  Raziyeh Keshavarz; Mahnaz Farahi
Journal:  RSC Adv       Date:  2022-01-27       Impact factor: 3.361

9.  TCCA-mediated oxidative rearrangement of tetrahydro-β-carbolines: facile access to spirooxindoles and the total synthesis of (±)-coerulescine and (±)-horsfiline.

Authors:  Manda Sathish; Akash P Sakla; Fabiane M Nachtigall; Leonardo S Santos; Nagula Shankaraiah
Journal:  RSC Adv       Date:  2021-05-05       Impact factor: 4.036

10.  Structural basis of the stereoselective formation of the spirooxindole ring in the biosynthesis of citrinadins.

Authors:  Zhiwen Liu; Fanglong Zhao; Boyang Zhao; Jie Yang; Joseph Ferrara; Banumathi Sankaran; B V Venkataram Prasad; Biki Bapi Kundu; George N Phillips; Yang Gao; Liya Hu; Tong Zhu; Xue Gao
Journal:  Nat Commun       Date:  2021-07-06       Impact factor: 14.919

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.