Anticancer thiosemicarbazones: chemical properties, interaction with iron metabolism, and resistance development

FS PapeVeronika, A EnyedyÉva… - Antioxidants & redox …, 2019 - liebertpub.com
Significance: During the past decades, thiosemicarbazones were clinically developed for a
variety of diseases, including tuberculosis, viral infections, malaria, and cancer. With regard …

[HTML][HTML] Thiazole, triazole, thio-and semicarbazone derivatives-Promising moieties for drug development for the treatment of tuberculosis

CB Scarim, FR Pavan - European Journal of Medicinal Chemistry Reports, 2021 - Elsevier
Thiazole, triazole, thio and semicarbazones are privileged motifs that act as
pharmacophores in bioactive compounds for various diseases, such as Tuberculosis (TB) …

[HTML][HTML] Exploring the synthesis, structure, spectroscopy and biological activities of novel 4-benzylidene-1-(2-(2, 4-dichloro phenyl) acetyl) thiosemicarbazide …

M Waheed, S Idris, F Jan, A Alam, M Ibrahim… - Saudi Pharmaceutical …, 2023 - Elsevier
Background Novel α-amylase inhibitors play a crucial role in managing diabetes and
obesity, contributing to improved public health by addressing these challenging and …

Design, synthesis, in vitro and in silico evaluation of a new series of oxadiazole-based anticancer agents as potential Akt and FAK inhibitors

MD Altıntop, B Sever, GA Çiftçi, G Turan-Zitouni… - European journal of …, 2018 - Elsevier
In the current work, new 1, 3, 4-oxadiazole derivatives were synthesized and investigated for
their cytotoxic effects on A549 human lung adenocarcinoma, C6 rat glioma and NIH/3T3 …

Design, synthesis, and evaluation of a new series of thiazole-based anticancer agents as potent Akt inhibitors

MD Altıntop, B Sever, G Akalın Çiftçi, A Özdemir - Molecules, 2018 - mdpi.com
In an attempt to develop potent anticancer agents targeting Akt, new thiazole derivatives (1–
10) were synthesized and investigated for their cytotoxic effects on A549 human lung …

Design, synthesis and biological evaluation of a new series of arylidene indanones as small molecules for targeted therapy of non-small cell lung carcinoma and …

MD Altıntop, A Özdemir, HE Temel… - European Journal of …, 2022 - Elsevier
In an attempt to identify small molecules for targeted therapy of non-small cell lung
carcinoma (NSCLC) and prostate cancer (PCa), new arylidene indanones (1–10) were …

Synthesis and biological evaluation of 2-nitrocinnamaldehyde derived thiosemicarbazones as urease inhibitors

M Islam, A Khan, M Khan, SA Halim, S Ullah… - Journal of Molecular …, 2023 - Elsevier
Hyperactivity of urease enzyme induces pathogenesis of peptic ulcers and gastritis. The
excess of urease can be reduced by introducing various inhibitors. The risk of high urease …

The synthesis of novel piperazine-benzodioxole substituted phthalocyanines and investigation of their α-amylase and tyrosinase inhibition properties

İ Değirmencioğlu, FO Tuncay, U Cakmak… - Journal of …, 2021 - Elsevier
Abstract In this study, novel 1-(benzo [d][1, 3] dioxol-5-ylmethyl) piperazine substituted
phthalocyanine Zn (II), Pb (II) and Co (II) complexes (ZnPc, PbPc, CoPc) were synthesized …

Development of a multi-target anticancer Sn (ii) pyridine-2-carboxaldehyde thiosemicarbazone complex

J Wu, T Yang, X Wang, W Li, M Pang, H Sun… - Dalton …, 2021 - pubs.rsc.org
In this study, we proposed to design effective multi-target anticancer agents based on the
chelation of nontoxic metals with ligands that possess anticancer activity. In total, five Sn (II) …

Pyrazole incorporated new thiosemicarbazones: Design, synthesis and investigation of DPP-4 inhibitory effects

B Sever, H Soybir, Ş Görgülü, Z Cantürk, MD Altıntop - Molecules, 2020 - mdpi.com
Dipeptidyl peptidase-4 (DPP-4) inhibition has been recognized as a promising approach to
develop safe and potent antidiabetic agents for the management of type 2 diabetes. In this …