Thiazole Modified Covalent Triazine Framework as Carcinogenic Metabolites Adsorbent: A Dft Insight DOI
Hasher Irshad, Muhammad Tehseen Azhar,

Katrine Qvotrup

et al.

Published: Jan. 1, 2024

Language: Английский

Thiazole Modified Covalent Triazine Framework as Carcinogenic Metabolites Adsorbent: A DFT Insight DOI
Hasher Irshad, Muhammad Tehseen Azhar, Katrine Qvortrup

et al.

Journal of Molecular Graphics and Modelling, Journal Year: 2025, Volume and Issue: 137, P. 109009 - 109009

Published: March 10, 2025

Language: Английский

Citations

0

Recent Progress in Thiazole, Thiosemicarbazone, and Semicarbazone Derivatives as Antiparasitic Agents Against Trypanosomatids and Plasmodium spp. DOI Creative Commons
Pamela Souza Tada da Cunha, Ana Luísa Rodriguez Gini, Chung Man Chin

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(8), P. 1788 - 1788

Published: April 16, 2025

Neglected tropical diseases (NTDs), including Chagas disease, human African trypanosomiasis (HAT), leishmaniasis, and malaria, remain a major global health challenge, disproportionately affecting low-income populations. Current therapies for these suffer from significant limitations, such as reduced efficacy, high toxicity, emerging parasite resistance, highlighting the urgent need new therapeutic strategies. In response, substantial efforts have been directed toward synthesis of molecules with improved potency, selectivity, pharmacokinetic profiles. However, despite many compounds exhibiting favorable ADMET (absorption, distribution, metabolism, excretion, toxicity) profiles strong in vitro activity, their translation into vivo models remains limited. Key challenges include lack investment, absence fully representative experimental models, difficulties extrapolating cell-based assay results to more complex biological systems. this review, we analyzed latest advancements (2019–2024) development compound classes, correlating predictive parameters observed activity. Among parameters, highlighted partition coefficient (LogP), which measures compound’s lipophilicity influences its ability cross membranes, Caco-2 cell permeability, an model widely used predict intestinal drug absorption. Additionally, prioritized most promising structural classes pharmaceutical development, discussing structure–activity relationships (SARs) remaining that must be overcome enable clinical application treatment NTDs.

Language: Английский

Citations

0

Recent studies on protein kinase signaling inhibitors based on thiazoles: review to date DOI Creative Commons
Manal S. Ebaid, Hoda Atef Abdelsattar Ibrahim, Asmaa F. Kassem

et al.

RSC Advances, Journal Year: 2024, Volume and Issue: 14(50), P. 36989 - 37018

Published: Jan. 1, 2024

Due to the important role of protein kinases in phosphorylation within vital cellular processes, their abnormal function, especially cancer situations, has underscored importance therapy.

Language: Английский

Citations

1

Design, synthesis and antifungal activity of novel vanillin derivatives containing thiazole and acylhydrazone moieties DOI
Ding Li, Xiaofang Yao, Weiwei Wang

et al.

Pest Management Science, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 4, 2024

Abstract BACKGROUND The potential application of vanillin as a fungicide has garnered significant attention in the agricultural product market and food industries. Consequently, novel series derivatives containing thiazole hydrazone fragments were strategically designed, synthesized, evaluated for their antifungal activity against six representative plant phytopathogenic fungi. RESULTS In vitro assay, some title showed good Botrytis cinerea , Fusarium solani Magnaporthe grisea . Significantly, compound 4a exhibited remarkable broad‐spectrum fungistatic potency displayed most potent B. F. with half maximal effective concentration (EC 50 ) values 1.07 0.78 μg/mL, respectively, substantially surpassing efficacy commercial hymexazol comparable to carbendazim. addition, 4k selectively inhibited M. lowest EC value 7.77 μg/mL. vivo assay revealed that superior protective compared At same time, scanning electron microscopy (SEM), transmission (TEM), fluorescent dye staining exerted its fungicidal by damaging cell wall, membrane mitochondria cinerea. CONCLUSION Modification through electron‐withdrawing group substitution hydrophobic substitution, followed condensation thiazole‐4‐carbohydrazide, could result highly active derivatives. Among them, which excellent inhibitory activities potentially serve lead compound. © 2024 Society Chemical Industry.

Language: Английский

Citations

0

Recent advances in the synthesis of nitrogen-containing heterocyclic compounds via multicomponent reaction and their emerging biological applications: a review DOI

Mallappa,

Mamta Chahar,

Nisha Choudhary

et al.

Journal of the Iranian Chemical Society, Journal Year: 2024, Volume and Issue: unknown

Published: Dec. 23, 2024

Language: Английский

Citations

0

Thiazole Modified Covalent Triazine Framework as Carcinogenic Metabolites Adsorbent: A Dft Insight DOI
Hasher Irshad, Muhammad Tehseen Azhar,

Katrine Qvotrup

et al.

Published: Jan. 1, 2024

Language: Английский

Citations

0