Multiple biological activities and molecular docking studies of newly synthesized 3-(pyridin-4-yl)-1H-pyrazole-5-carboxamide chalcone hybrids
R Sribalan, G Banuppriya, M Kirubavathi… - Bioorganic & Medicinal …, 2016 - Elsevier
A series of fifteen new chemical entities, 3-(pyridin-4-yl)-1H-pyrazole-5-carboxamide
chalcones (6a–o), were synthesized as new hybrids with enriched biological activities …
chalcones (6a–o), were synthesized as new hybrids with enriched biological activities …
Discovery of 4-benzyloxy and 4-(2-phenylethoxy) chalcone fibrate hybrids as novel PPARα agonists with anti-hyperlipidemic and antioxidant activities: Design …
In the current work, a series of novel 4-benzyloxy and 4-(2-phenylethoxy) chalcone fibrate
hybrids (10a-o) and (11a-e) were synthesized and evaluated as new PPARα agonists in …
hybrids (10a-o) and (11a-e) were synthesized and evaluated as new PPARα agonists in …
Recent developments by zinc based reagents/catalysts promoted organic transformations
The Lewis acids of the sort ZnX 2 (X= Cl, Br, OTf & I) are rather simple and mild yet proves its
efficiency in enabling wide range of synthetic transformations in organic synthesis …
efficiency in enabling wide range of synthetic transformations in organic synthesis …
Synthesis, analgesic, anti-inflammatory, COX/5-LOX inhibition, ulcerogenic evaluation, and docking study of benzimidazole bearing indole and benzophenone …
KMJ Nagesh, T Prashanth, HA Khamees… - Journal of Molecular …, 2022 - Elsevier
Inflammation therapy is particularly focused on the development of safer non-steroidal anti-
inflammatory drugs (NSAIDs), administered to control inflammation. It is typically considered …
inflammatory drugs (NSAIDs), administered to control inflammation. It is typically considered …
Design, synthesis and pharmacophoric model building of new 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamides with potential antiproliferative activity
MH Abdelrahman, AS Aboraia… - Chemical biology & …, 2017 - Wiley Online Library
Novel 3‐alkoxymethyl/3‐phenyl indole‐2‐carboxamide derivatives were synthesized and
evaluated for their anticancer activity. Most of the tested compounds showed moderate to …
evaluated for their anticancer activity. Most of the tested compounds showed moderate to …
Synthesis, in vitro and in vivo biological evaluation, COX-1/2 inhibition and molecular docking study of indole-N-acylhydrazone derivatives
ADT de Oliveira Moraes, MDS de Miranda… - Bioorganic & Medicinal …, 2018 - Elsevier
The objective of this work was to obtain and evaluate anti-inflammatory in vitro, in vivo and in
silico potential of novel indole-N-acylhydrazone derivatives. In total, 10 new compounds (3a …
silico potential of novel indole-N-acylhydrazone derivatives. In total, 10 new compounds (3a …
N′-((2-(6-bromo-2-oxo-2H-chromen-3-yl)-1H-indol-3-yl) methylene) benzohydrazide as a probable Bcl-2/Bcl-xL inhibitor with apoptotic and anti-metastatic potential
A wide number of marketed drugs and drug candidates in cancer clinical development
contain halogen substituents. The aim of the present study was to synthesize a series of …
contain halogen substituents. The aim of the present study was to synthesize a series of …
Inhibition of LPS-stimulated ROS production by fluorinated and hydroxylated chalcones in RAW 264.7 macrophages with structure-activity relationship study
Based on the importance of the previous fluorinated and/or hydroxylated chalcones studies,
thirty-six compounds were designed as phenyl or hydroxyphenyl bearing fluoro …
thirty-six compounds were designed as phenyl or hydroxyphenyl bearing fluoro …
Synthesis of new ibuprofen hybrid conjugates as potential anti-inflammatory and analgesic agents
SS Panda, AS Girgis, HH Honkanadavar… - Future Medicinal …, 2020 - Future Science
Background: A new set of hybrid conjugates derived from 2-(4-isobutylphenyl) propanoic
acid (ibuprofen) is synthesized to overcome the drawbacks of the current non-steroidal anti …
acid (ibuprofen) is synthesized to overcome the drawbacks of the current non-steroidal anti …
Studies of Cytotoxicity Effects, SARS‐CoV‐2 Main Protease Inhibition, and in Silico Interactions of Synthetic Chalcones
OL Guterres Fernandes, T Tizziani… - Chemistry & …, 2023 - Wiley Online Library
Abstract SARS‐CoV‐2 main protease (Mpro) plays an essential role in proteolysis cleavage
that promotes coronavirus replication. Thus, attenuating the activity of this enzyme …
that promotes coronavirus replication. Thus, attenuating the activity of this enzyme …