One‐pot and two‐pot methods for chalcone derived pyrimidines synthesis and applications

S Farooq, Z Ngaini - Journal of Heterocyclic Chemistry, 2021 - Wiley Online Library
Chalcone‐derived pyrimidine is a well‐known heterocyclic compound that is commonly
present in ribonucleic acid (RNA) and deoxyribonucleic acid (DNA) bio‐isosteres …

Discovery of highly potent tubulin polymerization inhibitors: Design, synthesis, and structure-activity relationships of novel 2, 7-diaryl-[1, 2, 4] triazolo [1, 5-a] …

XS Huo, XE Jian, J Ou-Yang, L Chen, F Yang… - European Journal of …, 2021 - Elsevier
Abstract By removing 5-methyl and 6-acetyl groups in our previously reported compound 3,
we designed a series of novel 2, 7-diaryl-[1, 2, 4] triazolo [1, 5-a] pyrimidine derivatives as …

Antibacterial and molecular docking studies of newly synthesized nucleosides and Schiff bases derived from sulfadimidines

HH Amer, EH Eldrehmy, SM Abdel-Hafez… - Scientific reports, 2021 - nature.com
A new series of nucleosides, moieties, and Schiff bases were synthesized from
sulfadimidine. Infrared (IR), 1HNMR, 13C NMR, and mass spectrometry techniques and …

Discovery and optimization of 2, 3-diaryl-1, 3-thiazolidin-4-one-based derivatives as potent and selective cytotoxic agents with anti-inflammatory activity

AM Shawky, FA Almalki, AN Abdalla… - European Journal of …, 2023 - Elsevier
Several studies have indicated the potential therapeutic outcomes of combining selective
COX-2 inhibitors with tubulin-targeting anticancer agents. In the current study, a novel series …

[HTML][HTML] Anticancer activity, spectroscopic and molecular docking of some new synthesized sugar hydrazones, Arylidene and α-Aminophosphonate derivatives

HH Amer, SH Alotaibi, AH Trawneh, AM Metwaly… - Arabian Journal of …, 2021 - Elsevier
In this work, we design and then synthesis of new derivatives of nucleosides, oxadiazoline
derivatives containing acetylated sugars and α-aminophosphonate derivatives. The …

Morpholine substituted quinazoline derivatives as anticancer agents against MCF-7, A549 and SHSY-5Y cancer cell lines and mechanistic studies

AR Dwivedi, V Kumar, V Prashar, A Verma… - RSC Medicinal …, 2022 - pubs.rsc.org
A series of morpholine substituted quinazoline derivatives have been synthesized and
evaluated for cytotoxic potential against A549, MCF-7 and SHSY-5Y cancer cell lines. These …

Synthesis and screening of novel 4-N-heterocyclic-2-aryl-6, 7, 8-trimethoxyquinazolines as antiproliferative and tubulin polymerization inhibitors

AR Dwivedi, SS Rawat, V Kumar, N Kumar… - Bioorganic & Medicinal …, 2022 - Elsevier
Colchicine binding site represent a crucial target for the anticancer drug development
especially in view of emerging drug resistance from the currently available …

Benzotriazole Substituted 2-Phenylquinazolines as Anticancer Agents: Synthesis, Screening, Antiproliferative and Tubulin Polymerization Inhibition Activity

AR Dwivedi, SS Rawat, V Kumar… - Current Cancer Drug …, 2023 - ingentaconnect.com
Aims: Development of anticancer agents targeting tubulin protein. Background: Tubulin
protein is being explored as an important target for anticancer drug development. Ligands …

Papain-Decorated Mucopenetrating SEDDS: A Tentative Approach to Combat Absorption Issues of Acyclovir via the Oral Route

A Mahmood, R Haneef, AZ Al Meslamani… - Pharmaceutics, 2022 - mdpi.com
The aim of the current study was to enhance the oral bioavailability of Acyclovir (ACV) based
on the papain-functionalized self-emulsifying drug delivery systems (SEDDS). The optimum …

KOtBu-mediated transition-metal-free synthesis of pyrimidines by selective three-component coupling reactions: A mechanistic insight

F Wang, Z Deng, Y Wang, F Yuan, X Zhang, GP Lu… - Tetrahedron, 2022 - Elsevier
A KO t Bu-mediated strategy for pyrimidine synthesis via selective three-component coupling
reactions has been disclosed. This chemistry, in which a series of pyrimidines (20 examples) …