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 …

[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 …

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 …

Novel pyrazolo[3,4-d]pyrimidines: design, synthesis, anticancer activity, dual EGFR/ErbB2 receptor tyrosine kinases inhibitory activity, effects on cell cycle profile and …

M Maher, AE Kassab, AF Zaher… - Journal of enzyme …, 2019 - Taylor & Francis
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 …

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 …

Comparison of the drug-drug interactions potential of erlotinib and gefitinib via inhibition of UDP-glucuronosyltransferases

Y Liu, J Ramírez, L House, MJ Ratain - Drug Metabolism and Disposition, 2010 - ASPET
We aimed to investigate and compare the effects of erlotinib and gefitinib on UDP-
glucuronosyltransferase (UGT) activities and to quantitatively evaluate their drug-drug …

Design strategies, structure activity relationship and mechanistic insights for purines as kinase inhibitors

S Sharma, J Singh, R Ojha, H Singh, M Kaur… - European journal of …, 2016 - Elsevier
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 …

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 …

Designing of kinase hinge binders: A medicinal chemistry perspective

V Sharma, M Gupta - Chemical Biology & Drug Design, 2022 - Wiley Online Library
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 …

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 …