Cis− trans isomerization of organic molecules and biomolecules: implications and applications

C Dugave, L Demange - Chemical reviews, 2003 - ACS Publications
Organic molecules as well as metal complexes may exist as several geometric isomers1
which display distinct physical properties and chemical reactivities. A molecule containing …

Hydrazone-based materials; DFT, TD-DFT, NBO analysis, fukui function, MESP analysis, and solar cell applications

MAS Sakr, FF Sherbiny, AAS El-Etrawy - Journal of Fluorescence, 2022 - Springer
Due to numerous pharmaceutical and biological activities hydrazone (TC) based materials,
it was important to investigate quantum chemical studies such as Density functional theory …

1-Acylthiosemicarbazides, 1, 2, 4-triazole-5 (4H)-thiones, 1, 3, 4-thiadiazoles and hydrazones containing 5-methyl-2-benzoxazolinones: synthesis, analgesic-anti …

U Salgın-Gökşen, N Gökhan-Kelekçi, Ö Göktaş… - Bioorganic & medicinal …, 2007 - Elsevier
Acetic acid hydrazide containing 5-methyl-2-benzoxazolinone (4) was synthesized by the
condensation of 2-(5-methyl-2-benzoxazolinone-3-yl) acetate with hydrazine hydrate …

Design, synthesis, DNA binding, modeling, anticancer studies and DFT calculations of Schiff bases tethering benzothiazole-1, 2, 3-triazole conjugates

MA Almehmadi, A Aljuhani, SY Alraqa, I Ali… - Journal of Molecular …, 2021 - Elsevier
In an attempt to design and prepare a new library of anticancer candidates, focused
thiopropargylated benzothiazole was reacted with ethyl azidoacetate and/or ethyl …

Design, Synthesis, and Pharmacological Evaluation of Novel N-Acylhydrazone Derivatives as Potent Histone Deacetylase 6/8 Dual Inhibitors

DA Rodrigues, GÀ Ferreira-Silva… - Journal of medicinal …, 2016 - ACS Publications
This manuscript describes a novel class of N-acylhydrazone (NAH) derivatives that act as
histone deacetylase (HDAC) 6/8 dual inhibitors and were designed from the structure of …

Rational design and synthesis of novel quinazolinone N-acetohydrazides as type II multi-kinase inhibitors and potential anticancer agents

SS Abd El-Karim, YM Syam, AM El Kerdawy… - Bioorganic …, 2024 - Elsevier
In the current investigation, a new class of quinazolinone N-acetohydrazides 9a-v was
designed as type II multi-kinase inhibitors. The target quinazolinones were tailored so that …

Design, synthesis and biological evaluation of novel isoniazid derivatives with potent antitubercular activity

F Martins, S Santos, C Ventura, R Elvas-Leitão… - European journal of …, 2014 - Elsevier
The disturbing emergence of multidrug-resistant strains of Mycobacterium tuberculosis (Mtb)
has been driving the scientific community to urgently search for new and efficient …

Synthesis and analgesic and anti-inflammatory activities 6-substituted-3 (2H)-pyridazinone-2-acetyl-2-(p-substituted/nonsubstituted benzal) hydrazone derivatives

M Gökçe, S Utku, E Küpeli - European journal of medicinal chemistry, 2009 - Elsevier
In this study new 6-substituted-3 (2H)-pyridazinone-2-acetyl-2-(p-substituted benzal)
hydrazone V derivatives were synthesized as analgesic and anti-inflammatory agents. The …

Design and biological evaluation of 3-substituted quinazoline-2,4(1H,3H)-dione derivatives as dual c-Met/VEGFR-2-TK inhibitors

A Hassan, FAF Mubarak, IA Shehadi… - Journal of Enzyme …, 2023 - Taylor & Francis
The dual c-Met/vascular endothelial growth factor receptor 2 (VEGFR-2) TK inhibition is a
good strategy to overcome therapeutic resistance to small molecules VEGFR-2 inhibitors. In …

Mechanochemical synthesis and biological evaluation of novel isoniazid derivatives with potent antitubercular activity

PFM Oliveira, B Guidetti, A Chamayou, C André-Barrès… - Molecules, 2017 - mdpi.com
A series of isoniazid derivatives bearing a phenolic or heteroaromatic coupled frame were
obtained by mechanochemical means. Their pH stability and their structural …