Caspase-3 activators as anticancer agents
N Srivastava, AK Saxena - Current Protein and Peptide Science, 2023 - ingentaconnect.com
Background: The cancer is still a major cause of death worldwide. Among different targets to
design anticancer agents, caspase-3 is an important target as its cleavage and activation …
design anticancer agents, caspase-3 is an important target as its cleavage and activation …
Polyoxometalate-based nanocomposites for antitumor and antibacterial applications
D Chang, Y Li, Y Chen, X Wang, D Zang, T Liu - Nanoscale Advances, 2022 - pubs.rsc.org
Polyoxometalates (POMs), as emerging inorganic metal oxides, have been shown to have
significant biological activity and great medicinal value. Nowadays, biologically active POM …
significant biological activity and great medicinal value. Nowadays, biologically active POM …
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 …
good strategy to overcome therapeutic resistance to small molecules VEGFR-2 inhibitors. In …
Synthesis and biological activity, and molecular modelling studies of potent cytotoxic podophyllotoxin-naphthoquinone compounds
HT Nguyen, QGN Thi, THN Thi, PH Thi… - RSC …, 2022 - pubs.rsc.org
A new approach for the synthesis of podophyllotoxin-naphthoquinone compounds using
microwave-assisted three-component reactions is reported in this study. Novel …
microwave-assisted three-component reactions is reported in this study. Novel …
New thieno [3, 2-d] pyrimidine-based derivatives: Design, synthesis and biological evaluation as antiproliferative agents, EGFR and ARO inhibitors inducing apoptosis …
AM Farghaly, OM AboulWafa, HH Baghdadi… - Bioorganic …, 2021 - Elsevier
An array of newly synthesized thieno [3, 2-d] pyrimidine-based derivatives and
thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were …
thienotriazolopyrimidines hybridized with some pharmacophoric anticancer fragments were …
Design, synthesis, and biological evaluation of 5-((8-methoxy-2-methylquinolin-4-yl) amino)-1H-indole-2-carbohydrazide derivatives as novel Nur77 modulators
B Li, J Yao, K Guo, F He, K Chen, Z Lin, S Liu… - European journal of …, 2020 - Elsevier
Nur77 is a potential target for the treatment of cancer such as HCC. Herein, we detailed the
discovery of a novel series of 5-((8-methoxy-2-methylquinolin-4-yl) amino)-1H-indole-2 …
discovery of a novel series of 5-((8-methoxy-2-methylquinolin-4-yl) amino)-1H-indole-2 …
Novel 3, 4-dihydro-4-oxoquinazoline-based acetohydrazides: Design, synthesis and evaluation of antitumor cytotoxicity and caspase activation activity
In search for novel small molecules with antitumor cytotoxicity via activating procaspase-3,
we have designed and synthesized three series of novel (E)-N′-benzylidene-4 …
we have designed and synthesized three series of novel (E)-N′-benzylidene-4 …
Design, synthesis and biological evaluation of methylenehydrazine-1-carboxamide derivatives with (5-((4-(pyridin-3-yl) pyrimidin-2-yl) amino)-1H-indole scaffold …
H Hu, J Wu, M Ao, X Zhou, B Li, Z Cui, T Wu, L Wang… - Bioorganic …, 2020 - Elsevier
In continuation of our previous work on the investigation of CDK9 inhibitors bearing indole
moiety for the discovery of novel anticancer agents, novel methylenehydrazine-1 …
moiety for the discovery of novel anticancer agents, novel methylenehydrazine-1 …
[HTML][HTML] Synthesis of Quinazolin-4 (3H)-ones via a novel approach
A Akbari, M Zahedifar - Journal of Saudi Chemical Society, 2023 - Elsevier
The present work was designed based on the new multi-component reaction, which forms 2-
aryl/alkyl-quinazolin-4 (3H)-ones in a one-pot reaction with good to excellent yields (86 …
aryl/alkyl-quinazolin-4 (3H)-ones in a one-pot reaction with good to excellent yields (86 …
Synthesis and biological evaluations of N′-substituted methylene-4-(quinoline-4-amino) benzoylhydrazides as potential anti-hepatoma agents
B Li, F Zhu, F He, Q Huang, X Liu, T Wu, T Zhao… - Bioorganic …, 2020 - Elsevier
In the effort to develop novel quinoline derivatives for the treatment of liver cancer, we
synthesized a series of N′-Substituted methylene-4-(quinoline-4-amino) …
synthesized a series of N′-Substituted methylene-4-(quinoline-4-amino) …