Medicinal significance of sp2/sp3 hybridized at C-3-substituted indole-containing lead molecules and FDA-approved drugs
Herein, the privilege in favor of biological importance of indole-containing scaffolds related
to the semi-synthetic and extracted from natural sources is summarized. Such compounds …
to the semi-synthetic and extracted from natural sources is summarized. Such compounds …
A Perspective of the Amide Group Containing FDA Approved Anticancer Drugs from 2021–2022 (A Review)
M Asif, R Srivastava, A Fatima, M Shakeel… - Russian Journal of …, 2023 - Springer
In this review, we describe a collection and assessment of 16 anticancer drugs approved by
the US FDA between 2021 to June 2022, which include small and big amide group …
the US FDA between 2021 to June 2022, which include small and big amide group …
Novel functionalized spiro [Indoline-3, 5′-pyrroline]-2, 2′ dione derivatives: synthesis, characterization, drug-likeness, ADME, and anticancer potential
A highly stereo-selective, one-pot, multicomponent method was chosen to synthesize the
novel functionalized 1, 3-cycloaddition spirooxindoles (SOXs)(4a–4h). Synthesized SOXs …
novel functionalized 1, 3-cycloaddition spirooxindoles (SOXs)(4a–4h). Synthesized SOXs …
Lewis base-catalyzed synthesis of highly functionalized spirooxindole-pyranopyrazoles and their in vitro anticancer studies
Herein, the one-step, multi-component reaction (MCR) of a series of spirooxindole-
pyranopyrazole derivatives (5a-g), via a Knoevenagel condensation and Michael addition …
pyranopyrazole derivatives (5a-g), via a Knoevenagel condensation and Michael addition …
Synthesis of Functionalized 2′, 5‐Oxo‐spiro [furan‐2, 3′‐indoline]‐3‐carboxylate Derivatives as Antiproliferative Agents: ADMET Studies, and Molecular Docking …
Herein, we present a one‐pot, three‐component synthesis of spirooxindole‐oxofuran
carboxylate derivatives (4 a–d) through the Huisgen reaction. The newly synthesized …
carboxylate derivatives (4 a–d) through the Huisgen reaction. The newly synthesized …
[HTML][HTML] Recent Advances in the Synthesis of Pyrazoline Derivatives from Chalcones as Potent Pharmacological Agents: A Comprehensive Review
The pyrazoline scaffold plays a vital role in heterocyclic chemistry as a fundamental building
block in both organic and medicinal chemistry. A pyrazoline scaffold is composed of an …
block in both organic and medicinal chemistry. A pyrazoline scaffold is composed of an …
Solvent solute interaction (IEFPCM model), Michael addition-based anticancer drug synthesis, FTIR, NMR, and UV–visible investigations of spirooxindole …
P Manikandan, M Kumar, P Swarnamughi… - Journal of Molecular …, 2024 - Elsevier
Herein, click chemistry was chosen to synthesize 2AIPC using Knoevenegel and Michael
addition reactions. In this synthesis, Lewis base was attracted by the generation of sp 3 …
addition reactions. In this synthesis, Lewis base was attracted by the generation of sp 3 …
Synthesis of highly functionalized imine-containing halogen-substituted-1-oxo-acenaphthenes and their quantum computational investigation as propitious drugs for …
Herein, the one-keto protected and one-keto transformed into the imine-functionalized Schiff
bases (7a–b) through the 1, 2-dimethoxy-1, 2-dihydroacenaphthylene using calcium oxo …
bases (7a–b) through the 1, 2-dimethoxy-1, 2-dihydroacenaphthylene using calcium oxo …
[HTML][HTML] Isatin Bis-Imidathiazole Hybrids Identified as FtsZ Inhibitors with On-Target Activity Against Staphylococcus aureus
In the present study, a series of isatin bis-imidathiazole hybrids was designed and
synthesized to develop a new class of heterocyclic compounds with improved antimicrobial …
synthesized to develop a new class of heterocyclic compounds with improved antimicrobial …
In-silico screening of Staphylococcus aureus antibacterial agents based on Isatin scaffold: QSAR, molecular docking, molecular dynamics simulation and DFT …
L Emami, S Sadeghian, P Mardaneh, F Zare… - Molecular …, 2024 - Taylor & Francis
The design of novel antimicrobial drugs is necessary due to the increasing resistance to
many existing antibiotics. Considering that the drug discovery process requires a lot of time …
many existing antibiotics. Considering that the drug discovery process requires a lot of time …