EGFR is a potential dual molecular target for cancer and Alzheimer's disease
HJ Choi, YJ Jeong, J Kim, HS Hoe - Frontiers in Pharmacology, 2023 - frontiersin.org
Many researchers are attempting to identify drugs that can be repurposed as effective
therapies for Alzheimer's disease (AD). Several recent studies have highlighted epidermal …
therapies for Alzheimer's disease (AD). Several recent studies have highlighted epidermal …
[HTML][HTML] The challenges and the promise of molecular targeted therapy in malignant gliomas
H Wang, T Xu, Y Jiang, H Xu, Y Yan, D Fu, J Chen - Neoplasia, 2015 - Elsevier
Malignant gliomas are the most common malignant primary brain tumors and one of the
most challenging forms of cancers to treat. Despite advances in conventional treatment, the …
most challenging forms of cancers to treat. Despite advances in conventional treatment, the …
Neuregulin-1-mediated autocrine signaling underlies sensitivity to HER2 kinase inhibitors in a subset of human cancers
TR Wilson, DY Lee, L Berry, DS Shames, J Settleman - Cancer cell, 2011 - cell.com
HER2 kinase inhibitors, such as lapatinib, have demonstrated clinical efficacy in HER2-
amplified breast cancers. By profiling nearly 700 human cancer cell lines, we identified a …
amplified breast cancers. By profiling nearly 700 human cancer cell lines, we identified a …
Novel pyrazolo[3,4-d]pyrimidines: design, synthesis, anticancer activity, dual EGFR/ErbB2 receptor tyrosine kinases inhibitory activity, effects on cell cycle profile and …
A series of novel pyrazolo [3, 4-d] pyrimidines was synthesised. Twelve synthesised
compounds were evaluated for their anticancer activity against 60 human tumour cell lines …
compounds were evaluated for their anticancer activity against 60 human tumour cell lines …
Design, synthesis and antitumor activity of novel pyrazolo [3, 4-d] pyrimidine derivatives as EGFR-TK inhibitors
MA Abdelgawad, RB Bakr, OA Alkhoja… - Bioorganic chemistry, 2016 - Elsevier
Abstract A novel series of 2-(3, 6-dimethyl-1-phenyl-1H-pyrazolo [3, 4-d] pyrimidin-4-yloxy)-
N-(4-substitutedbenzylidene) acetohydrazide (12a–g) was prepared and their structures …
N-(4-substitutedbenzylidene) acetohydrazide (12a–g) was prepared and their structures …
Comparison of the drug-drug interactions potential of erlotinib and gefitinib via inhibition of UDP-glucuronosyltransferases
We aimed to investigate and compare the effects of erlotinib and gefitinib on UDP-
glucuronosyltransferase (UGT) activities and to quantitatively evaluate their drug-drug …
glucuronosyltransferase (UGT) activities and to quantitatively evaluate their drug-drug …
Design strategies, structure activity relationship and mechanistic insights for purines as kinase inhibitors
Kinases control a diverse set of cellular processes comprising of reversible phosphorylation
of proteins. Protein kinases play a pivotal role in human tumor cell proliferation, migration …
of proteins. Protein kinases play a pivotal role in human tumor cell proliferation, migration …
Discovery of 2-(6-{[(6-Fluoroquinolin-2-yl)methyl]amino}bicyclo[3.1.0]hex-3-yl)-N-hydroxypyrimidine-5-carboxamide (CHR-3996), a Class I Selective Orally Active …
D Moffat, S Patel, F Day, A Belfield… - Journal of medicinal …, 2010 - ACS Publications
A novel series of HDAC inhibitors demonstrating class I subtype selectivity and good oral
bioavailability is described. The compounds are potent enzyme inhibitors (IC50 values less …
bioavailability is described. The compounds are potent enzyme inhibitors (IC50 values less …
Designing of kinase hinge binders: A medicinal chemistry perspective
Protein kinases are key regulators of cellular signaling and play a critical role in
oncogenesis. Inhibitors of protein kinases are pursued by both industry and academia as a …
oncogenesis. Inhibitors of protein kinases are pursued by both industry and academia as a …
Liposomal form of erlotinib for local inhalation administration and efficiency of its transport to the lungs
J Szabová, O Mišík, J Fučík, K Mrázová… - International Journal of …, 2023 - Elsevier
This contribution is focused on the preparation of a liposomal drug delivery system of
erlotinib resisting the nebulization process that could be used for local treatment of non …
erlotinib resisting the nebulization process that could be used for local treatment of non …