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Structure-Based Design and Synthesis of 3Amino-1,5-Dihydro4Hpyrazolopyridin-4-One Derivatives as Tyrosine Kinase 2 Inhibitors

doi 10.1021/acs.jmedchem.5b01857.s001

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Structure-Based Design and Synthesis of 3Amino-1,5-Dihydro4Hpyrazolopyridin-4-One Derivatives as Tyrosine Kinase 2 Inhibitors

doi 10.1021/acs.jmedchem.5b01857.s001

Full Text

Abstract

Date

Authors

Publisher

Related search

Structure-Based Design of 6Chloro-4-Aminoquinazoline-2-Carboxamide Derivatives as Potent and Selective P21-Activated Kinase 4 (PAK4) Inhibitors

Synthesis of 3-Amino-1,5-Benzodiazepine-2-One Derivatives From Dehydroalanine Derivatives

Synthesis and in Vitro Cytotoxicity of the 4-(Halogenoanilino)-6-Bromoquinazolines and Their 6-(4-Fluorophenyl) Substituted Derivatives as Potential Inhibitors of Epidermal Growth Factor Receptor Tyrosine Kinase

Design, Synthesis and Structure–activity Relationship of 2-(3′,4′,5′-Trimethoxybenzoyl)-Benzo[b]furan Derivatives as a Novel Class of Inhibitors of Tubulin Polymerization

DESIGN AND SYNTHESIS OF NEW EGFR- TYROSINE KINASE INHIBITORS CONTAINING PYRAZOLO[3,4-d]PYRIMIDINE CORES AS ANTICANCER AGENTS

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