Evaluating the Cytotoxic Effects of Some Chlorinated Substituted 2-Amino-3-carbonitrile Chromene Derivatives on 3T3 and MCF-7 Cell Lines

Cancer remains a leading cause of death worldwide, necessitating novel therapeutic approaches. In this study we synthesized and characterized 2-amino-3-carbonitrile chromene derivatives and evaluated their cytotoxic effects on 3T3 and MCF-7 cell lines. Characterization included melting point, IR, NMR, and elemental analysis. Cytotoxicity was assessed via MTT assay, with IC50 values calculated, while apoptosis induction was confirmed by flow cytometry using annexin V/propidium iodide staining. Compounds 4f and 4h demonstrated significant cytotoxicity against breast cancer cells, with IC50 values of 4.74 and 21.97 µg/ml and selectivity indices of 3.83 and 2.80, respectively. Increased apoptotic cell populations support their pro-apoptotic potential. These findings indicate that the chromene derivatives, synthesized via a one-pot method, may serve as promising candidates for further anticancer drug development.

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Journal
Acta chimica slovenica
Published
2025-09-18
DOI
https://doi.org/10.17344/acsi.2025.9331
Primary Topic
Synthesis of Organic Compounds
Type
article
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article

Evaluating the Cytotoxic Effects of Some Chlorinated Substituted 2-Amino-3-carbonitrile Chromene Derivatives on 3T3 and MCF-7 Cell Lines

Salehe Sabouri, Behzad Behnam, Mehdi Abaszadeh, Yasaman Abolhassani et al.
Acta chimica slovenica
Synthesis of Organic Compounds
article

Evaluating the Cytotoxic Effects of Some Chlorinated Substituted 2-Amino-3-carbonitrile Chromene Derivatives on 3T3 and MCF-7 Cell Lines

Salehe Sabouri, Behzad Behnam, Mehdi Abaszadeh, Yasaman Abolhassani, Bagher Amirheidari, Fatemeh Haghani, Arghavan Arjomand Kermani, Ali‐Reza Armin
article en

Abstract

Cancer remains a leading cause of death worldwide, necessitating novel therapeutic approaches. In this study we synthesized and characterized 2-amino-3-carbonitrile chromene derivatives and evaluated their cytotoxic effects on 3T3 and MCF-7 cell lines. Characterization included melting point, IR, NMR, and elemental analysis. Cytotoxicity was assessed via MTT assay, with IC50 values calculated, while apoptosis induction was confirmed by flow cytometry using annexin V/propidium iodide staining. Compounds 4f and 4h demonstrated significant cytotoxicity against breast cancer cells, with IC50 values of 4.74 and 21.97 µg/ml and selectivity indices of 3.83 and 2.80, respectively. Increased apoptotic cell populations support their pro-apoptotic potential. These findings indicate that the chromene derivatives, synthesized via a one-pot method, may serve as promising candidates for further anticancer drug development.

Acta chimica slovenicaVol. 72(3)
Kerman University of Medical Sciences (IR), Melbourn Science Park (GB), Iron Mountain (United States) (US), Howell Laboratories (United States) (US), American Rock Mechanics Association (US), Yaroslavl State Agricultural Academy (RU), Pharmaceutical Biotechnology (Czechia) (CZ), Gojo (France) (FR)
Openalex Percentile: Top 71%
Synthesis of Organic Compounds
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Evaluating the Cytotoxic Effects of Some Chlorinated Substituted 2-Amino-3-carbonitrile Chromene Derivatives on 3T3 and MCF-7 Cell Lines — Salehe Sabouri, Behzad Behnam, et al. · Acta chimica slovenica (2025) | TGRS Research Map | TGRS