Synthetic α-glucosidase inhibitors as promising anti-diabetic agents: Recent developments and future challenges

A Mushtaq, U Azam, S Mehreen, MM Naseer - European journal of …, 2023 - Elsevier
Diabetes mellitus is one of the biggest challenges for the scientific community in the 21st
century. It is a well-recognized multifactorial health problem contributes significantly to high …

Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview

M Dhameja, P Gupta - European journal of medicinal chemistry, 2019 - Elsevier
Abstract α-Glucosidase enzyme inhibition is an effective therapeutic decorum in the
treatment of type 2 diabetes mellitus. Since 1990, three α-glucosidase inhibitors are known …

Novel 1, 2, 4-triazole derivatives as potential anticancer agents: Design, synthesis, molecular docking and mechanistic studies

HAM El-Sherief, BGM Youssif, SNA Bukhari… - Bioorganic …, 2018 - Elsevier
A series of novel compounds carrying 1, 2, 4-triazole scaffold was synthesized and
evaluated for their anticancer activity against a panel of cancer cell lines using MTT assay …

Potential anticancer agents against melanoma cells based on an as-synthesized thiosemicarbazide derivative

P Kozyra, A Korga-Plewko, Z Karczmarzyk, A Hawrył… - Biomolecules, 2022 - mdpi.com
In this paper, thiosemicarbazide derivatives were synthesized as potential anticancer
agents. X-ray investigations for 1-(2, 4-dichlorophenoxy) acetyl-4-(2-fluorophenyl) …

Isatin based thiosemicarbazide derivatives as potential inhibitor of α-glucosidase, synthesis and their molecular docking study

F Rahim, M Taha, N Iqbal, S Hayat, F Qureshi… - Journal of Molecular …, 2020 - Elsevier
A new series of isatin based thiosemicarbazide derivatives 1–15 were synthesized and
characterized by 1 H NMR, 13 C NMR and HR-EIMS. The synthetic derivatives were …

α-Glucosidase and α-amylase inhibition, molecular modeling and pharmacokinetic studies of new quinazolinone-1, 2, 3-triazole-acetamide derivatives

A Yavari, M Mohammadi-Khanaposhtani… - Medicinal Chemistry …, 2021 - Springer
In this study, a new series of quinazolinone-1, 2, 3-triazole-acetamide hybrids 8a–m, using
by molecular hybridization of the potent α-glucosidase inhibitor pharmacophores, was …

Novel phenoxyacetylthiosemicarbazide derivatives as novel ligands in cancer diseases

P Kozyra, G Adamczuk, Z Karczmarzyk… - Toxicology and Applied …, 2023 - Elsevier
Numerous epidemiological studies report an increased risk of developing prostate cancer in
patients with melanoma and an increased risk of developing melanoma in patients with …

Synthesis, in vitro screening and docking studies of new thiosemicarbazide derivatives as antitubercular agents

M Pitucha, Z Karczmarzyk, M Swatko-Ossor, W Wysocki… - Molecules, 2019 - mdpi.com
A series of thiosemicarbazide derivatives was designed and synthesized by reaction of
carboxylic acid hydrazide with isothiocyanates. The molecular structures of the investigated …

[HTML][HTML] 1, 2, 4-Triazolin-5-thione derivatives with anticancer activity as CK1γ kinase inhibitors

M Pitucha, M Janeczko, K Klimek, E Fornal, M Wos… - Bioorganic …, 2020 - Elsevier
The optimization and synthesis of new CK2 and CK1 inhibitors are the basis for the
development of new therapeutic strategies for the treatment of cancer and …

Evaluation of developmental toxicity in zebrafish embryos and antiproliferative potential against human tumor cell lines of new derivatives containing 4-nitrophenyl …

A Szopa, M Herbet, A Pachuta-Stec… - Toxicology and Applied …, 2023 - Elsevier
The aim of the studies was to evaluate the antiproliferative potential against human tumor
cell lines of newly synthetized derivatives containing 4-nitrophenyl group, as well as its …