| 1 |
O16291Advances in Synthesis and anti-Alzheimer's Potential of Functionalized Benzofurans: A Recent Overview |
Synlett |
DOI: 10.1055/a-2522-0970 |
2025 |
| 2 |
O16277Overview of Phenylhydrazine-Based Organic Transformations |
ChemistrySelect |
10/1 |
2025 |
| 3 |
O16273Application of Post-Ugi Transformation Strategies Towards the Synthesis and Functionalization of 2,5-Diketopiperazines |
Tetrahedron |
134067 |
2024 |
| 4 |
O16274Co(II) and Cu(II) Porphyrins Catalysed the Synthesis of Quinoline and Naphthoxazine via Dehydrogenative Reactions |
Current Organic Chemistry |
29/3 |
2024 |
| 5 |
O16275Quinoline as a Privileged Structure: A Recent Update on Synthesis and Biological Activities |
Current Topics in Medicinal Chemistry |
24/27 |
2024 |
| 6 |
O16276Synthetic Approaches Toward Imidazo-Fused Heterocycles: A Comprehensive Review |
Journal of Heterocyclic Chemistry |
61/11 |
2024 |
| 7 |
O16272Unveiling of Indanone-Benzimidazole Hybrids as Anti-Alzheimer's Agents: Computational and Experimental Studies |
ChemistrySelect |
9/15 |
2024 |
| 8 |
O16271Visible-light-mediated synthesis of functionalized benzofurans: an update |
Chemistry of Heterocyclic Compounds |
60 |
2024 |
| 9 |
O162781, 3-Thiazole Derivatives as a Promising Scaffold in Medicinal Chemistry: A Recent Overview |
Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry |
22 |
2023 |
| 10 |
O16279Benzofuran pyran hybrid prevents glucocorticoid induced osteoporosis in mice via modulation of canonical Wnt/β-catenin signaling |
Apoptosis |
27 |
2022 |
| 11 |
O16280Benzofuran pyran compound rescues rat and human osteoblast from lipotoxic effect of palmitate by inhibiting lipid biosynthesis and promoting stabilization of RUNX2 |
Toxicology in Vitro |
66 |
2020 |
| 12 |
O16282Synthesis, biological evaluation and molecular dynamic simulations of novel Benzofuran-tetrazole derivatives as potential agents against Alzheimer’s disease. |
Bioorganic & Medicinal Chemistry Letters |
29 |
2019 |
| 13 |
O16281Synthesis, biological evaluation, structure−activity relationship, and mechanism of action studies of Quinoline−Metronidazole derivatives against experimental visceral leishmaniasis |
J. Med. Chem. |
62 |
2019 |
| 14 |
O16286In-house chemical library repurposing: A case example for Pseudomonas aeruginosa antibiofilm activity and quorum sensing inhibition. |
Drug Dev Res. |
1 |
2018 |
| 15 |
O16285Synthesis and bio-evaluation of indole-chalcone based benzopyrans as promising antiligase and antiproliferative agents. |
European Journal of Medicinal Chemistry |
143 |
2018 |
| 16 |
O16284Synthesis and evaluation of novel triazolyl quinoline derivatives as potential antileishmanial agents. |
European Journal of Medicinal Chemistry |
154 |
2018 |
| 17 |
O16283Synthesis and study of Benzofuran-Pyran analogs as BMP-2 targeted osteogenic agents. |
European Journal of Medicinal Chemistry |
156 |
2018 |
| 18 |
O16287The diacylglycerol acyltransferase Rv3371 of Mycobacterium tuberculosis is required for growth arrest and involved in stress induced cell wall alterations. |
Tuberculosis |
104 |
2017 |
| 19 |
O16288Development of Leishmania donovani stably expressing DsRed for flow cytometry-based drug screening using chalcone thiazolyl-hydrazone as a new antileishmanial target. |
Int J Antimicrob Agents |
48 |
2016 |
| 20 |
O16289Hybrids of coumarin–indole: design, synthesis and biological evaluation in Triton WR-1339 and highfat diet induced hyperlipidemic rat models. |
MedChemComm |
7 |
2016 |
| 21 |
O16290Novel Chalcone−Thiazole Hybrids as Potent Inhibitors of Drug Resistant Staphylococcus aureus. |
ACS Medicinal Chemistry Letters |
6 |
2015 |
