Therapeutic potential of quinazoline derivatives for Alzheimer's disease: A comprehensive review
Quinazolines are considered as a promising class of bioactive heterocyclic compounds with
broad properties. Particularly, the quinazoline scaffold has an impressive role in the design …
broad properties. Particularly, the quinazoline scaffold has an impressive role in the design …
Quinazoline: An update on current status against convulsions
Epilepsy is one of the most frequent chronic neurological disorder extremely threatening the
life and good health. More than 70 million individuals suffering from epilepsy worldwide and …
life and good health. More than 70 million individuals suffering from epilepsy worldwide and …
Design, synthesis, and biological evaluation of novel quinoline derivatives as small molecule mutant EGFR inhibitors targeting resistance in NSCLC: In vitro screening …
RA Kardile, AP Sarkate, DK Lokwani, SV Tiwari… - European Journal of …, 2023 - Elsevier
Here in, we report the design, synthesis and in vitro anticancer activity of a novel series of 24
quinoline analogues of substituted amide and sulphonamide derivatives. The anticancer …
quinoline analogues of substituted amide and sulphonamide derivatives. The anticancer …
Computational and Synthetic approach with Biological Evaluation of Substituted Quinoline derivatives as small molecule L858R/T790M/C797S triple mutant EGFR …
KS Karnik, AP Sarkate, SV Tiwari, R Azad… - Bioorganic …, 2021 - Elsevier
New substituted quinoline derivatives were designed and synthesized via a five-step
modified Suzuki coupling reaction. A comparative molecular docking study was carried out …
modified Suzuki coupling reaction. A comparative molecular docking study was carried out …
Free energy perturbation guided Synthesis with Biological Evaluation of Substituted Quinoline derivatives as small molecule L858R/T790M/C797S mutant EGFR …
KS Karnik, AP Sarkate, SV Tiwari, R Azad… - Bioorganic Chemistry, 2021 - Elsevier
Two different schemes of novel substituted quinoline derivatives were designed and
synthesized via simple reaction steps and conditions. A comparative molecular docking …
synthesized via simple reaction steps and conditions. A comparative molecular docking …
Novel nickel (II) and copper (II) coordination compounds of 2–phenylquinazoline–4–carboxylate: Synthesis and characterization
Two novel compounds [Ni (PQC) 2 (H 2 O) 2]. H 2 O and [Cu (PQC) 2] where PQC= 2–
phenylquinazoline–4–carboxylate have been synthesized. Magnetic susceptibility …
phenylquinazoline–4–carboxylate have been synthesized. Magnetic susceptibility …
Recyclable Magnetic Cu-MOF-74-Catalyzed C(sp2)-N Coupling and Cyclization under Microwave Irradiation: Synthesis of Imidazo[1,2-c]quinazolines and Their …
Magnetic Cu-MOF-74 (Fe3O4@ SiO2@ Cu-MOF-74) was synthesized for the first time by
grafting MOF-74 (copper as the metal center) on the surface of core-shell magnetic carboxyl …
grafting MOF-74 (copper as the metal center) on the surface of core-shell magnetic carboxyl …
An insight into sustainable and green chemistry approaches for the synthesis of quinoline derivatives as anticancer agents
B Kumaraswamy, K Hemalatha, R Pal… - European Journal of …, 2024 - Elsevier
Quinolones, a key class of heterocyclics, are gaining popularity among organic and
medicinal chemists due to their promising properties. Quinoline, with its broad spectrum of …
medicinal chemists due to their promising properties. Quinoline, with its broad spectrum of …
Molecular dynamic simulations based discovery and development of thiazolidin-4-one derivatives as EGFR inhibitors targeting resistance in non-small cell lung …
KS Karnik, AP Sarkate, DK Lokwani… - Journal of …, 2023 - Taylor & Francis
Targeting kinases with oncogenic driver mutations in malignancies with allosteric kinase
inhibitors is a promising new treatment technique. EGFR inhibitors targeting the …
inhibitors is a promising new treatment technique. EGFR inhibitors targeting the …
Synthesis and hydrolytic decomposition of 2-hetaryl[1,2,4]triazolo[1,5-c]quinazolines: DFT study
OO Pylypenko, LK Sviatenko, KP Shabelnyk… - Structural Chemistry, 2024 - Springer
Mechanisms for formation and hydrolysis of biologically active 2-substituted [1, 2, 4] triazolo
[1, 5-c] quinazolines were modeled at the SMD/B3LYP/6–31+ G (d) theory level. Obtained …
[1, 5-c] quinazolines were modeled at the SMD/B3LYP/6–31+ G (d) theory level. Obtained …