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Croatica Chemica Acta, Vol. 94 No. 1, 2021.

Izvorni znanstveni članak

https://doi.org/10.5562/cca3758

Synthesis and Biological Evaluation of Indolyl Bis-chalcones as Anti-Breast Cancer and Antioxidant Agents

Pravin S. Bhale orcid id orcid.org/0000-0003-3639-0357 ; Department of Chemistry, Yeshwantrao Chavan Mahavidyalaya, Tuljapur, Dist-Osmanabad-413601, Maharashtra, India
Hemant V. Chavan ; Department of Chemistry, A.S.P. College, Devrukh, Dist-Ratnagiri-415 804, Maharashtra, India
Rupali S. Endait ; Department of Chemistry, Radhabai Kale Mahila Mahavidyalaya, Ahmednagar-414001, Maharashtra, India
Ashok T. Kadam ; Department of Chemistry, Yeshwantrao Chavan Mahavidyalaya, Tuljapur, Dist-Osmanabad-413601, Maharashtra, India
Rajesh J. Bopalkar ; Department of Chemistry, Yeshwantrao Chavan Mahavidyalaya, Tuljapur, Dist-Osmanabad-413601, Maharashtra, India
Mandar S. Gaikwad ; Department of Chemistry, Yeshwantrao Chavan Mahavidyalaya, Tuljapur, Dist-Osmanabad-413601, Maharashtra, India

Puni tekst: engleski pdf 2.274 Kb

str. 35-41

preuzimanja: 339

citiraj

Sažetak

A series of novel α-cyano substituted indolyl bis-chalcones (3a−l) has been synthesized and evaluated for their in vitro antitumor activity against the human breast cancer MCF7 (estrogen receptor-positive) and normal Vero cell lines using sulforhodamine B (SRB) assay method. Compounds 3a, 3c and 3d showed potent activity (GI50 = 11.7, 15.3 and 17.9 µM respectively) against the human breast cancer MCF7 cell line, which was almost as good as that of adriamycin (GI50 = < 0.1 µM) whereas, screening against the normal Vero Monkey cell line showed moderate selectivity. Furthermore, all the synthesized compounds screened for their antioxidant potential against DPPH, NO, SOR, and H2O2 radicals. Most of the bis-chalcones exhibited significant DPPH (51.09−12.72 %) and NO (64.11−34.43 %) radical scavenging activity and modest activity against SOR (88.08−43.14 %) and H2O2 (80.13−56.0 %) radicals compared to the reference standard ascorbic acid (40.78 %, 42.63 %, 87.05 %, and 79.42 % respectively). Current study provides impetus for the development of highly potent indolyl bis-chalcone derivatives as anticancer leads.

This work is licensed under a Creative Commons Attribution 4.0 International License.

Ključne riječi

indolyl bis-chalcone; breast cancer; anti-cancer activity; antioxidant activity

Hrčak ID:

269952

URI

https://hrcak.srce.hr/269952

Datum izdavanja:

28.6.2021.

Posjeta: 882 *