Design, synthesis and biological evaluation of novel thiosemicarbazone-indole derivatives targeting prostate cancer cells
ZX He, JL Huo, YP Gong, Q An, X Zhang, H Qiao… - European Journal of …, 2021 - Elsevier
To discover novel anticancer agents with potent and low toxicity, we designed and
synthesized a range of new thiosemicarbazone-indole analogues based on lead compound …
synthesized a range of new thiosemicarbazone-indole analogues based on lead compound …
Novel thiosemicarbazone derivatives containing indole fragment as potent and selective anticancer agent
Z He, H Qiao, F Yang, W Zhou, Y Gong, X Zhang… - European Journal of …, 2019 - Elsevier
Potent and safe anticancer drugs research and development are still on the way to human
health. In this report, a series of novel thiosemicarbazone derivatives containing indole …
health. In this report, a series of novel thiosemicarbazone derivatives containing indole …
Design and synthesis of phenylpiperazine derivatives as potent anticancer agents for prostate cancer
Abstract Novel thiourea (5a, 5b) and thiazolidinone derivatives (6a, 6b) were synthesized by
hybridizing molecules starting from the compound 6‐(4‐phenylpiperazin‐1‐yl) pyridin‐3 …
hybridizing molecules starting from the compound 6‐(4‐phenylpiperazin‐1‐yl) pyridin‐3 …
Design, synthesis, cytotoxic screening and molecular docking studies of novel hybrid thiosemicarbazone derivatives as anticancer agents
FZ Mohammed, YW Rizzk, IM El Deen… - Chemistry & …, 2021 - Wiley Online Library
Thiosemicarbazones have been the focus of scientists owing to their broad clinical
anticancer range. Herein, A Series of new thiosemicarbazone derivatives 5–9 were …
anticancer range. Herein, A Series of new thiosemicarbazone derivatives 5–9 were …
Design, synthesis and in vitro evaluation of new thiosemicarbazone derivatives as potential anticancer agents
Thiosemicarbazones play a pivotal role as potential therapeutic agents for the management
of lung cancer. 4-(4-Cyanophenyl)-1-[(5-arylfuran-2-yl) methylene] thiosemicarbazides (1 …
of lung cancer. 4-(4-Cyanophenyl)-1-[(5-arylfuran-2-yl) methylene] thiosemicarbazides (1 …
3, 5-Disubstituted-thiazolidine-2, 4-dione analogs as anticancer agents: design, synthesis and biological characterization
A series of 2, 5-disubstituted-thiazolidine-2, 4-dione analogs based on the newly identified
lead 1, a potential anticancer agent via the inhibition of the Raf/MEK/extracellular signal …
lead 1, a potential anticancer agent via the inhibition of the Raf/MEK/extracellular signal …
Thiosemicarbazone-based lead optimization to discover high-efficiency and low-toxicity anti-gastric cancer agents
XH Zhang, YY Tao, Q Ma, HJ Wang, ZX He… - European Journal of …, 2020 - Elsevier
In this paper, a series of thiosemicarbazone derivatives containing different aromatic
heterocyclic groups were synthesized and the tridentate donor system of the lead compound …
heterocyclic groups were synthesized and the tridentate donor system of the lead compound …
Design and Synthesis of Novel Cytotoxic Indole‐Thiosemicarbazone Derivatives: Biological Evaluation and Docking Study
In this work, two novel series of indole‐thiosemicarbazone derivatives were designed,
synthesized, and evaluated for their cytotoxic activity against MCF‐7, A‐549, and Hep‐G2 …
synthesized, and evaluated for their cytotoxic activity against MCF‐7, A‐549, and Hep‐G2 …
Discovery of thiosemicarbazone-containing compounds with potent anti-proliferation activity against drug-resistant K562/A02 cells
X Gu, X Li, M Guan, C Jiang, Q Song, N Sun… - Bioorganic & Medicinal …, 2020 - Elsevier
Abstract P-glycoprotein (P-gp)-mediated multidrug resistance (MDR) is a major obstacle to
successful chemotherapy for leukemia. In this study, a series of thiosemicarbazone …
successful chemotherapy for leukemia. In this study, a series of thiosemicarbazone …
Design, synthesis, biological and computational assessment of new thiazolidin‐4‐one derivatives as potential anticancer agents through the apoptosis pathway
A variety of novel thiazolidin‐4‐one himachalene derivatives were designed and
synthesized through hetero‐cyclization of thiosemicarbazone analogs that have previously …
synthesized through hetero‐cyclization of thiosemicarbazone analogs that have previously …
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