2H/4H-Chromenes—A versatile biologically attractive Scaffold

V Raj, J Lee - Frontiers in Chemistry, 2020 - frontiersin.org
2H/4H-chromene (2H/4H-ch) is an important class of heterocyclic compounds with versatile
biological profiles, a simple structure, and mild adverse effects. Researchers discovered …

Synthetic strategies and pharmacological activities of chromene and its derivatives: An overview

MK Katiyar, GK Dhakad, S Arora, S Bhagat… - Journal of Molecular …, 2022 - Elsevier
Chromene is commonly found in nature and is considered one of the most frequently used
scaffolds in heterocyclic chemistry for the designing of chemical probes for therapeutic and …

From antibacterial to antitumour agents: a brief review on the chemical and medicinal aspects of sulfonamides

H Azevedo-Barbosa, DF Dias, LL Franco… - Mini Reviews in …, 2020 - ingentaconnect.com
Sulfonamides have been in clinical use for many years, and the development of bioactive
substances containing the sulfonamide subunit has grown steadily in view of their important …

Design and Synthesis of Sulfanilamide Aminophosphonates as Novel Antibacterial Agents towards Escherichia coli

J Wang, MF Ansari, JM Lin… - Chinese Journal of …, 2021 - Wiley Online Library
Main observation and conclusion The limit ability of traditional antibiotics to treat drug
resistant bacteria calls for new therapeutic alternatives. A class of unique sulfanilamide …

Design, green synthesis, molecular docking and anticancer evaluations of diazepam bearing sulfonamide moieties as VEGFR-2 inhibitors

NM Saleh, MSA El-Gaby, K El‐Adl… - Bioorganic …, 2020 - Elsevier
Novel series of diazepam bearing sulfonamide moieties 5 af and 7 ac were designed,
synthesized and evaluated for anticancer activity against HepG2, HCT-116 and MCF-7 cell …

Design, synthesis, molecular docking, in silico ADMET profile and anticancer evaluations of sulfonamide endowed with hydrazone-coupled derivatives as VEGFR-2 …

AM Sayed, FA Taher, MRK Abdel-Samad… - Bioorganic …, 2021 - Elsevier
A new series of sulfonamide endowed with hydrazone coupled to dimethyl and/or diethyl
malonates were prepared. Various sulfa drugs were diazotized and followed by coupling …

Design, Synthesis, Biological Evaluation, and Molecular Modeling of Novel 4H-Chromene Analogs as Potential Succinate Dehydrogenase Inhibitors

T Lu, Y Yan, T Zhang, G Zhang, T Xiao… - Journal of Agricultural …, 2021 - ACS Publications
Thirty-one new 4 H-chromene derivatives were designed and synthesized. Their structures
were identified with IR, 1H NMR, 13C NMR, and HRMS. The crystal structure of compound …

Purine/purine isoster based scaffolds as new derivatives of benzamide class of HDAC inhibitors

K Nepali, TY Chang, MJ Lai, KC Hsu, Y Yen… - European Journal of …, 2020 - Elsevier
This study reports the design, synthesis and evaluation of a series of histone deacetylase
(HDAC) inhibitors containing purine/purine isoster as a capping group and an N-(2 …

Synthesis and DFT calculations of linear and nonlinear optical responses of novel 2-thioxo-3-N,(4-methylphenyl) thiazolidine-4 one

B Baroudi, K Argoub, D Hadji… - Journal of Sulfur …, 2020 - Taylor & Francis
The aim of this work is to present results of both experimental and theoretical studies of 2–
thioxo–3–N,(4–methylphenyl) thiazolidine–4–one. In this paper, we present the chemical …

Introducing of novel class of pyrano[2,3-c]pyrazole-5-carbonitrile analogs with potent antimicrobial activity, DNA gyrase inhibition, and prominent pharmacokinetic …

M Almaghrabi, A Musa, AKB Aljohani… - Journal of …, 2024 - Taylor & Francis
Microbiological DNA gyrase is recognized as an exceptional microbial target for the
innovative development of low-resistant and more effective antimicrobial drugs. Hence, we …