Design and synthesis of spirooxindole–pyrrolidines embedded with indole and pyridine heterocycles by multicomponent reaction: anticancer and in silico studies

Mayakrishnan, Sivakalai and Kathirvelan, Devarajan and Arun, Yuvaraj and et al, . (2022) Design and synthesis of spirooxindole–pyrrolidines embedded with indole and pyridine heterocycles by multicomponent reaction: anticancer and in silico studies. New Journal of Chemistry, 46 (21). pp. 10089-10106. ISSN 1144-0546

[img] Text
New_Journal_of_Chemistry.pdf - Published Version
Restricted to Registered users only

Download (9MB) | Request a copy

Abstract

Owing to the downsides of existing anticancer drugs, it is necessary to find more effective and selective anticancer agents for researchers in medicinal chemistry worldwide. Spirooxindoles are poised as privileged scaffolds because they exist in many natural products and bioactive molecules. Herein, we report an efficient, environment-friendly route for synthesizing a series of spirooxindoles using the 1,3-dipolar cycloaddition reaction of a dipolarophile with in situ generated azomethine ylide using ethanol as a solvent without any catalyst. The reaction offers potent biologically active spirooxindole fused with indole and pyridine heterocycles in good to excellent yield (69-94%) with higher diastereoselectivity. These synthesized compounds (4a-x) were screened for anticancer activity using A549, HepG-2, and SKOV-3 cancer cell lines using the MTT assay. Among all the screened compounds, 4u and 4w displayed substantial cytotoxic activity against HepG-2 cells at less than 10 μg mL−1. Molecular docking studies with the Bcl-2 and ALK receptor revealed that the higher binding energy was observed for 4u and 4w, and 4c and 4o with a value of −6.56 and −8.41, −6.73, and −7.14 kcal mol−1, respectively. Considering all the data, compounds 4u and 4w, 4c and 4o possess potent anticancer activity against respective receptors and can be the promising lead compounds for cancer drug discovery. © 2022 The Royal Society of Chemistry

[error in script]
IITH Creators:
IITH CreatorsORCiD
Item Type: Article
Additional Information: Sivakalai Mayakrishnan acknowledges the CSIR, India, for providing a Senior Research Fellowship (Grant No. 31/6(422)/2017-EMR-I) and TATA-CSIR-Open Source Drug Discovery (TCOF). Uma Maheswari Narayanan acknowledges Major Lab Project (MLP-12 Organic & Bioorganic Chemistry) CSIR-CLRI toward purchasing chemicals. PY thanks Science and Engineering Research Board (SERB) New Delhi, India (GPP 0334 –Ref. No: EEQ/2017/000161) for financial support.
Uncontrolled Keywords: Anti-cancer agents; Anticancer activities; Anticancer drug; Heterocycles; In-silico; Medicinal chemistry; Multicomponents; Natural products; Pyrrolidines; Silico studies
Subjects: Chemistry
Divisions: Department of Chemistry
Depositing User: . LibTrainee 2021
Date Deposited: 11 Oct 2022 11:45
Last Modified: 11 Oct 2022 11:45
URI: http://raiith.iith.ac.in/id/eprint/10893
Publisher URL: http://doi.org/10.1039/d1nj05839h
OA policy: https://v2.sherpa.ac.uk/id/publication/18027
Related URLs:

    Actions (login required)

    View Item View Item
    Statistics for RAIITH ePrint 10893 Statistics for this ePrint Item