Structure-activity relationship (SAR) study and design strategies of nitrogen-containing heterocyclic moieties for their anticancer activities

J Akhtar, AA Khan, Z Ali, R Haider, MS Yar - European journal of medicinal …, 2017 - Elsevier
The present review article offers a detailed account of the design strategies employed for the
synthesis of nitrogen-containing anticancer agents. The results of different studies describe …

[HTML][HTML] A comprehensive review on pyrazoline based heterocyclic hybrids as potent anticancer agents

K Haider, M Shafeeque, S Yahya, MS Yar - European Journal of Medicinal …, 2022 - Elsevier
Cancer is one of the leading causes of death globally, around 10 million deaths are reported
every year due to cancer. Some clinically approved anticancer drugs play a riveting role in …

Design, synthesis, molecular docking and biological activity evaluation of some novel indole derivatives as potent anticancer active agents and apoptosis inducers

AMS El-Sharief, YA Ammar, A Belal… - Bioorganic …, 2019 - Elsevier
Abstract Reaction of 5-morphilinosulfonylisatin (1) with acetophenones (2a–e) afforded 3-
hydroxy-3-substituted-2-oxoindoles 3a-e, when treated with acetic acid the expected 3 …

Synthesis and anticancer activity of thiourea derivatives bearing a benzodioxole moiety with EGFR inhibitory activity, apoptosis assay and molecular docking study

SY Abbas, RAK Al-Harbi, MAMS El-Sharief - European Journal of …, 2020 - Elsevier
New thiourea derivatives bearing a benzodioxole moiety were synthesized via the reaction
of 5-isothiocyanatobenzodioxole with amino compounds such as aromatic amines, sulfa …

One-pot synthesis and molecular docking of some new spiropyranindol-2-one derivatives as immunomodulatory agents and in vitro antimicrobial potential with DNA …

MA Salem, A Ragab, AA Askar, A El-Khalafawy… - European Journal of …, 2020 - Elsevier
Abstract a series of 2-oxospiro [indoline-3, 4′-pyran] derivatives 4 and 7 were obtained in
good yield under mild conditions from the one-pot reaction of indole-2, 3-dione derivatives 1 …

The therapeutic journey of pyridazinone

W Akhtar, M Shaquiquzzaman, M Akhter… - European journal of …, 2016 - Elsevier
Pyridazinones have drawn a substantial attention within the field of research analysis and
development. The moiety is a subject matter of intensive research because of its wide …

[HTML][HTML] Virtual screening in drug-likeness and structure/activity relationship of pyridazine derivatives as Anti-Alzheimer drugs

A Zerroug, S Belaidi, I BenBrahim, L Sinha… - Journal of King Saud …, 2019 - Elsevier
Virtual screening emerged as an important tool in our quest to access successful CNS
medicaments for treating Alzheimer's disease. The computational techniques applied in this …

Pyridazinone: an important element of pharmacophore possessing broad spectrum of activity

S Dubey, PA Bhosle - Medicinal Chemistry Research, 2015 - Springer
In the last few years, the pyridazine derivatives have been found to exhibit a wide range of
pharmacological activities. A large number of research articles and patents described them …

Synthesis and cytotoxic activities of some pyrazoline derivatives bearing phenyl pyridazine core as new apoptosis inducers

RF George, MA Fouad, IEO Gomaa - European journal of medicinal …, 2016 - Elsevier
The cyclization of chalcones 3a-3u with 3-hydrazinyl-6-phenylpyridazine 7 under basic
condition led to the formation of new pyrazoline derivatives 8a-8u. All final compounds were …

Sulphonamides: Deserving class as MMP inhibitors?

P Jain, C Saravanan, SK Singh - European Journal of Medicinal Chemistry, 2013 - Elsevier
The importance of sulphonamide moiety in medicinal chemistry cannot be ignored as it
constitutes an important class of extensively used drugs. Recently, sulphonamides have …