Emerging impact of triazoles as anti-tubercular agent
Tuberculosis, a disease of poverty is a communicable infection with a reasonably high
mortality rate worldwide. 10 Million new cases of TB were reported with approx 1.4 million …
mortality rate worldwide. 10 Million new cases of TB were reported with approx 1.4 million …
A mini review on pharmacological significance of isatin-1, 2, 3-triazole hybrids
Molecular hybridization is one of the recent stratagems in medicinal chemistry to synthesize
a novel hybrid molecule having better affinity and efficacy by combining two or more …
a novel hybrid molecule having better affinity and efficacy by combining two or more …
Anticancer effects with molecular docking confirmation of newly synthesized isatin sulfonamide molecular hybrid derivatives against hepatic cancer cell lines
The current study investigated the cytotoxic effect of ten sulfonamide-derived isatins,
following molecular hybridization, based on the association principles, on hepatocellular …
following molecular hybridization, based on the association principles, on hepatocellular …
The effect of 1, 2, 4-triazole-3-thiol derivatives bearing hydrazone moiety on cancer cell migration and growth of melanoma, breast, and pancreatic cancer spheroids
A Šermukšnytė, K Kantminienė, I Jonuškienė… - Pharmaceuticals, 2022 - mdpi.com
4-Phenyl-3-[2-(phenylamino) ethyl]-1 H-1, 2, 4-triazole-5 (4 H)-thione was used as a starting
compound for the synthesis of the corresponding 1, 2, 4-triazol-3-ylthioacetohydrazide …
compound for the synthesis of the corresponding 1, 2, 4-triazol-3-ylthioacetohydrazide …
Phenoxy pendant isatins as potent α-glucosidase inhibitors: reciprocal carbonyl⋯ carbonyl interactions, antiparallel π⋯ π stacking driven solid state self-assembly and …
Carbonyl–carbonyl (CO⋯ CO) interactions are recently explored noncovalent interactions of
significant interest owing to their role in the stability of biomacromolecules. Currently …
significant interest owing to their role in the stability of biomacromolecules. Currently …
Computational investigation into structural, topological, electronic properties, and biological evaluation of spiro [1H-indole-3, 2′-3H-1, 3-benzothiazole]-2-one
The current work comprises theoretical studies on spiro [1H-indole-3, 2′-3H-1, 3-
benzothiazole]-2-one employing density functional theory (DFT). The optimized structure …
benzothiazole]-2-one employing density functional theory (DFT). The optimized structure …
Synthesis, in vitro antimicrobial evaluation, and molecular docking studies of new isatin-1, 2, 3-triazole hybrids
T El Malah, H Farag, BA Hemdan, REA Mageid… - Journal of Molecular …, 2022 - Elsevier
Antibiotic resistance is rapidly evolving at an alarming rate, posing a severe threat to
humanity. In an effort to develop compounds with antimicrobial activity, we synthesized a …
humanity. In an effort to develop compounds with antimicrobial activity, we synthesized a …
Anticancer and Antiphytopathogenic Activity of Fluorinated Isatins and Their Water-Soluble Hydrazone Derivatives
AV Bogdanov, M Neganova, A Voloshina… - International Journal of …, 2023 - mdpi.com
A series of new fluorinated 1-benzylisatins was synthesized in high yields via a simple one-
pot procedure in order to explore the possible effect of ortho-fluoro (3a), chloro (3b), or bis …
pot procedure in order to explore the possible effect of ortho-fluoro (3a), chloro (3b), or bis …
Assembling a Cinnamyl Pharmacophore in the C3-Position of Substituted Isatins via Microwave-Assisted Synthesis: Development of a New Class of Monoamine …
A Manoharan, JM Oh, F Benny, S Kumar… - Molecules, 2023 - mdpi.com
Monoamine oxidase (MAO, EC 1.4. 3.4) is responsible for the oxidative breakdown of both
endogenous and exogenous amines and exists in MAO-A and MAO-B isomers. Eighteen …
endogenous and exogenous amines and exists in MAO-A and MAO-B isomers. Eighteen …
[HTML][HTML] Isatin-based ibuprofen and mefenamic acid Schiff base derivatives as dual inhibitors against urease and α–glucosidase: In vitro, in silico and cytotoxicity …
S Daud, M Saadullah, M Fakhar-e-Alam… - Journal of Saudi …, 2024 - Elsevier
Abstract α-Glucosidase and urease inhibitors have emerged as crucial for develo**
therapeutic drugs targeting diabetes and gastrointestinal disorders. This study reports on …
therapeutic drugs targeting diabetes and gastrointestinal disorders. This study reports on …