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Quantitative Structure−Activity Relationship of Flavonoid Analogues. 3. Inhibition of p56lck Protein Tyrosine Kinase
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3838(199801)17:01<07::aid-qsar7>3.0.co;2-nopenalex-snapshot
Quantitative Structure-Activity Relationship of Flavonoid Inhibitors of p56lck Protein Tyrosine Kinase: A Classical/Quantum Chemical Approach
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Piceatannol (3,4,3′,5′-tetrahydroxy-trans-stilbene) is a naturally occurring protein-tyrosine kinase inhibitor
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Signal transduction by receptors with tyrosine kinase activity
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A rational approach to the design of flavones as xanthine oxidase inhibitors
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Protein modification: phosphorylation on tyrosine residues
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The Beilstein Structure Registry System. 1. General design
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The Structure-Property Models Can Be Improved Using the Orthogonalized Descriptors
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The Use of the Ordered Orthogonalized Multivariate Linear Regression in a Structure−Activity Study of Coumarin and Flavonoid Derivatives as Inhibitors of Aldose Reductase
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Quantitative Structure−Activity Relationship of Flavonoid p56lck Protein Tyrosine Kinase Inhibitors. A Neural Network Approach
inferredcites →https://doi.org/10.1021/cr950202ropenalex-snapshot
Quantum-Chemical Descriptors in QSAR/QSPR Studies
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Dihydropyrimidine calcium channel blockers. 3. 3-Carbamoyl-4-aryl-1,2,3,4-tetrahydro-6-methyl-5-pyrimidinecarboxylic acid esters as orally effective antihypertensive agents
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Inhibition of Proteiin-Tyrosine Kinase Activity by Flavanoids and Related Compounds
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Protein-Tyrosine Kinase Inhibition: Mechanism-Based Discovery of Antitumor Agents
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Thymic tumorigenesis induced by overexpression of p56lck.
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The Protein Kinase Family: Conserved Features and Deduced Phylogeny of the Catalytic Domains
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The Molecular Genetics of Cancer
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Tyrosine Kinase Inhibition: An Approach to Drug Development
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Induction of Ectopic Eyes by Targeted Expression of the eyeless Gene in Drosophila
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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ChemInform Abstract: Quantitative Structure—Activity Relationship of Flavonoid Analogues. Part 3. Inhibition of p56lck Protein Tyrosine Kinase.
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