Biological importance of imidazole nucleus in the new millennium

B Narasimhan, D Sharma, P Kumar - Medicinal Chemistry Research, 2011 - Springer
Imidazole nucleus is a constituent of many bioactive heterocyclic compounds that are of
wide interest because of their diverse biological and clinical applications. This created …

Imatinib-ULS-lysozyme: a proximal tubular cell-targeted conjugate of imatinib for the treatment of renal diseases

MEM Dolman, KMA Van Dorenmalen… - Journal of controlled …, 2012 - Elsevier
The anticancer drug imatinib is an inhibitor of the platelet-derived growth factor receptor
(PDGFR) kinases, which are involved in the pathogenesis of fibrotic diseases. In the current …

Utility of sulfachloropyridazine in the synthesis of novel anticancer agents as antiangiogenic and apoptotic inducers

SS Zahran, FA Ragab, AM Soliman, MG El-Gazzar… - Bioorganic …, 2024 - Elsevier
In a search for new anticancer agents with better activity and selectivity, the present work
described the synthesis of several new series of sulfachloropyridazine hybrids with …

Synthesis and biological evaluation of N-(4-hydroxy-3-mercaptonaphthalen-1-yl) amides as inhibitors of angiogenesis and tumor growth

F Xu, Y Jia, Q Wen, X Wang, L Zhang, Y Zhang… - European Journal of …, 2013 - Elsevier
A series of N-(4-hydroxy-3-mercaptonaphthalen-1-yl) amides were synthesized and
investigated for their in vitro antiangiogenic activity. Among these compounds, 6d, which …

SAR studies of 4-pyridyl heterocyclic anilines that selectively induce autophagic cell death in von Hippel-Lindau-deficient renal cell carcinoma cells

M Bonnet, JU Flanagan, DA Chan, EW Lai… - Bioorganic & medicinal …, 2011 - Elsevier
We recently identified a class of pyridyl aniline thiazoles (PAT) that displayed selective
cytotoxicity for von Hippel-Lindau (VHL) deficient renal cell carcinoma (RCC) cells in vitro …

On the ability of imatinib mesylate to inhibit smooth muscle cell proliferation without delaying endothelialization: an in vitro study

K Vallières, É Petitclerc, G Laroche - Vascular pharmacology, 2009 - Elsevier
Restenosis, the re-occlusion of a diseased vessel following a surgical intervention, is a
major cause of failure of angioplasty, stenting, and bypass grafting with natural and synthetic …

Design, synthesis and optimization of new CXCR1/2 receptors antagonists for the treatment of exudative AMD

M Fabre - 2021 - theses.hal.science
In western countries, exudative age-related macular degeneration (AMD) is one of the
leading causes of blindness in the elderly. This disease is characterized by an abnormal …

[PDF][PDF] 2-Methylsulfanyl-4-(3-pyridyl) pyrimidine

RJ Du, JQ Wang, S Bi, YX Zhou… - … Section E: Structure …, 2009 - journals.iucr.org
organic compounds Page 1 2-Methylsulfanyl-4-(3-pyridyl)pyrimidine Ren-Jun Du, Jian-Qiang
Wang, Sheng Bi, Yi-Xin Zhou and Cheng Guo* College of Science, Nanjing University of …

Synthesis and Antibacterial, Anti-inflammatory and Anti-oxidant activity of 4-Acetamido-N-(3-Substituted-4-Fluorophenyl) Benzamides

J Raghavendra, PS Bhadbhade… - Asian Journal of …, 2014 - indianjournals.com
The extensive use of antimicrobial drugs resulted in drug resistance that threatens to reverse
the miracles of the last half century. To counteract the resistance produced by microbes …

[图书][B] CNS penetration of tyrosine kinase inhibitors in mouse models

M Elmeliegy - 2012 - search.proquest.com
For the past three decades, advances in the treatment of central nervous system (CNS)
tumors such as malignant glioma have only been modest. One particular challenge facing …