Highlights on steroidal arylidene derivatives as a source of pharmacologically active compounds: A review
V Brito, G Alves, P Almeida, S Silvestre - Molecules, 2021 - mdpi.com
Steroids constitute a unique class of chemical compounds, playing an important role in
physiopathological processes, and have high pharmacological interest. Additionally …
physiopathological processes, and have high pharmacological interest. Additionally …
Synthesis of 3β, 7α, 11α-trihydroxy-pregn-21-benzylidene-5-en-20-one derivatives and their cytotoxic activities
LH Shan, HM Liu, KX Huang, GF Dai, C Cao… - Bioorganic & medicinal …, 2009 - Elsevier
A series of novel 3β, 7α, 11α-trihydroxy-pregn-21-benzylidene-5-en-20-one derivatives were
synthesized and characterized by NMR, HRMS. The pregnenolone (1) was first …
synthesized and characterized by NMR, HRMS. The pregnenolone (1) was first …
Design, synthesis and evaluation of novel 16-imidazolyl substituted steroidal derivatives possessing potent diversified pharmacological properties
R Bansal, S Guleria, S Thota, SL Bodhankar… - Steroids, 2012 - Elsevier
As a part of our investigations into the structural–activity relationship studies of a novel class
of medicinally active 16-substituted steroids, several new 16-imidazolyl substituted steroidal …
of medicinally active 16-substituted steroids, several new 16-imidazolyl substituted steroidal …
Investigations on 16-arylideno steroids as a new class of neuroprotective agents for the treatment of Alzheimer's and Parkinson's diseases
Neuroinflammatory mechanisms mediated by activated glial and cytokines (TNF-α, IL-1β)
might contribute to neuronal degeneration leading to Alzheimer's (AD) and Parkinson's …
might contribute to neuronal degeneration leading to Alzheimer's (AD) and Parkinson's …
The Use of Switchable Polarity Solvents for the Synthesis of 16‐Arylidene Steroids via Claisen–Schmidt Condensation
Switchable polarity recyclable solvent mixtures were applied as reaction medium and
catalyst to replace the conventional base catalysts in the Claisen–Schmidt condensation of …
catalyst to replace the conventional base catalysts in the Claisen–Schmidt condensation of …
[HTML][HTML] Novel 4-azaandrostenes as prostate cancer cell growth inhibitors: Synthesis, antiproliferative effects, and molecular docking studies
V Brito, AO Santos, P Almeida… - Comptes …, 2019 - comptes-rendus.academie-sciences …
Résumé In this study, synthesis, structural characterization, molecular docking studies, and
antiproliferative effects in four different cell lines of several novel 16-arylidene-4-azaandrost …
antiproliferative effects in four different cell lines of several novel 16-arylidene-4-azaandrost …
Synthesis of 16E-[3-methoxy-4-(2-aminoethoxy) benzylidene] androstene derivatives as potent cytotoxic agents
R Bansal, S Guleria - Steroids, 2008 - Elsevier
The synthesis and cytotoxic studies of a new series of 16E-arylidene androstene derivatives
are reported herein. The impact of incorporating bis-tertiary amino functionalities in the …
are reported herein. The impact of incorporating bis-tertiary amino functionalities in the …
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
H Guo, H Wu, J Yang, Y Xiao, HJ Altenbach, G Qiu… - Steroids, 2011 - Elsevier
A series of new 16E-arylidene androstane derivatives were synthesized and characterized.
The new compounds were screened for their anticancer activities against the human cancer …
The new compounds were screened for their anticancer activities against the human cancer …
Synthesis and antileukemic activity of 16E-[4-(2-carboxy) ethoxybenzylidene]-androstene amides
R Bansal, PC Acharya - Steroids, 2012 - Elsevier
In order to determine the structural requirements for cytotoxicity against various tumor cell
lines, a new series of 16E-arylidene androstene amides with varying degrees of …
lines, a new series of 16E-arylidene androstene amides with varying degrees of …
Synthesis and biological evaluation of 16E-arylidenosteroids as cytotoxic and anti-aromatase agents
R Bansal, S Guleria, S Thota, RW Hartmann… - Chemical and …, 2011 - jstage.jst.go.jp
Taking into consideration the structural requirements for cytotoxicity and aromatase
inhibition, several new 16E-arylidenosteroidal derivatives have been prepared and …
inhibition, several new 16E-arylidenosteroidal derivatives have been prepared and …