Design, synthesis, and cytotoxic evaluation of new thiosemicarbazone/thiazolidin-4-one derivatives on PC3 cells

The combined synthetic, computational, and biological results demonstrate that thiazolidin-4-one-based hybrids, particularly compound 9, are promising selective androgen receptor-targeted anticancer agents, warranting further optimization and development.

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Publication Details

Journal
Future Medicinal Chemistry
Published
2025-11-24
DOI
https://doi.org/10.1080/17568919.2025.2592533
Citations
1
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
1.52
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article

Design, synthesis, and cytotoxic evaluation of new thiosemicarbazone/thiazolidin-4-one derivatives on PC3 cells

Pelin ŞAHİN, Halil Şenol, Şeyma Ateşoğlu, Fahri Akbaş et al.
1 citations
Future Medicinal Chemistry
Prostate Cancer Treatment and Research
1.52
article

Design, synthesis, and cytotoxic evaluation of new thiosemicarbazone/thiazolidin-4-one derivatives on PC3 cells

Pelin ŞAHİN, Halil Şenol, Şeyma Ateşoğlu, Fahri Akbaş, Feyzi Sinan Tokalı
article en
1 citations

Abstract

The combined synthetic, computational, and biological results demonstrate that thiazolidin-4-one-based hybrids, particularly compound 9, are promising selective androgen receptor-targeted anticancer agents, warranting further optimization and development.

Future Medicinal ChemistryVol. 17(24)
Kafkas University (TR), Bezmiâlem Vakıf Üniversitesi (TR)
Openalex Percentile: Top 13%
Prostate Cancer Treatment and Research
1.52
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