Overview of recent strategic advances in medicinal chemistry
G Wu, T Zhao, D Kang, J Zhang, Y Song… - Journal of medicinal …, 2019 - ACS Publications
Introducing novel strategies, concepts, and technologies that speed up drug discovery and
the drug development cycle is of great importance both in the highly competitive …
the drug development cycle is of great importance both in the highly competitive …
Targeting the HGF/Met signaling pathway in cancer therapy
F Cecchi, DC Rabe, DP Bottaro - Expert opinion on therapeutic …, 2012 - Taylor & Francis
Introduction: Under normal conditions, hepatocyte growth factor (HGF)-induced activation of
its cell surface receptor, the Met tyrosine kinase (TK), is tightly regulated by paracrine ligand …
its cell surface receptor, the Met tyrosine kinase (TK), is tightly regulated by paracrine ligand …
Software and resources for computational medicinal chemistry
C Liao, M Sitzmann, A Pugliese… - Future medicinal …, 2011 - Taylor & Francis
Computer-aided drug design plays a vital role in drug discovery and development and has
become an indispensable tool in the pharmaceutical industry. Computational medicinal …
become an indispensable tool in the pharmaceutical industry. Computational medicinal …
Hierarchical virtual screening approaches in small molecule drug discovery
A Kumar, KYJ Zhang - Methods, 2015 - Elsevier
Virtual screening has played a significant role in the discovery of small molecule inhibitors of
therapeutic targets in last two decades. Various ligand and structure-based virtual screening …
therapeutic targets in last two decades. Various ligand and structure-based virtual screening …
Measuring and interpreting the selectivity of protein kinase inhibitors
LA Smyth, I Collins - Journal of chemical biology, 2009 - Springer
Protein kinase inhibitors are a well-established class of clinically useful drugs, particularly
for the treatment of cancer. Achieving inhibitor selectivity for particular protein kinases often …
for the treatment of cancer. Achieving inhibitor selectivity for particular protein kinases often …
(−)-Oleocanthal as a c-Met inhibitor for the control of metastatic breast and prostate cancers
AY Elnagar, PW Sylvester, KA El Sayed - Planta medica, 2011 - thieme-connect.com
The proto-oncogene receptor tyrosine kinase c-Met encodes the high-affinity receptor for
hepatocyte growth factor (HGF). Dysregulation of the HGF‐c-Met pathway plays a significant …
hepatocyte growth factor (HGF). Dysregulation of the HGF‐c-Met pathway plays a significant …
Computational approaches for protein function prediction: a combined strategy from multiple sequence alignment to molecular docking-based virtual screening
The functional characterization of proteins represents a daily challenge for biochemical,
medical and computational sciences. Although finally proved on the bench, the function of a …
medical and computational sciences. Although finally proved on the bench, the function of a …
Synthesis and c-Met kinase inhibition of 3, 5-disubstituted and 3, 5, 7-trisubstituted quinolines: identification of 3-(4-acetylpiperazin-1-yl)-5-(3-nitrobenzylamino)-7 …
Y Wang, J Ai, Y Wang, Y Chen, L Wang… - Journal of medicinal …, 2011 - ACS Publications
By use of an improved synthetic strategy, a series of 3, 5-disubstituted and 3, 5, 7-
trisubstituted quinolines were readily prepared. 3, 5, 7-Trisubstituted quinolines 21a− c, 21l …
trisubstituted quinolines were readily prepared. 3, 5, 7-Trisubstituted quinolines 21a− c, 21l …
MET Exon 14 Mutation Encodes an Actionable Therapeutic Target in Lung Adenocarcinoma
Targeting somatically activated oncogenes has revolutionized the treatment of non–small
cell lung cancer (NSCLC). Mutations in the gene mesenchymal–epithelial transition (MET) …
cell lung cancer (NSCLC). Mutations in the gene mesenchymal–epithelial transition (MET) …
Discovery andw biological evaluation of novel 6, 7-disubstituted-4-(2-fluorophenoxy) quinoline derivatives possessing 1, 2, 3-triazole-4-carboxamide moiety as c-Met …
S Zhou, H Liao, M Liu, G Feng, B Fu, R Li… - Bioorganic & Medicinal …, 2014 - Elsevier
Abstract A series of 6, 7-disubstituted-4-(2-fluorophenoxy) quinoline derivatives possessing
1, 2, 3-triazole-4-carboxamide moiety were designed, synthesized and evaluated for their in …
1, 2, 3-triazole-4-carboxamide moiety were designed, synthesized and evaluated for their in …