(PDF) Discovery of Aminoquinazolines as Potent, Orally

Discovery of Aminoquinazolines as Potent, Orally Bioavailable Inhibitors of Lymphocyte-Specific Kinase: Synthesis, Structure-Activity Relationship, and in Vivo Anti-Inflammatory Activity

doi 10.1021/jm0605482.s001

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Discovery of Aminoquinazolines as Potent, Orally Bioavailable Inhibitors of Lymphocyte-Specific Kinase: Synthesis, Structure-Activity Relationship, and in Vivo Anti-Inflammatory Activity

doi 10.1021/jm0605482.s001

Full Text

Abstract

Date

Authors

Publisher

Related search

Discovery of a New Class of Highly Potent Inhibitors of Acid Ceramidase: Synthesis and Structure–Activity Relationship (SAR)

Design and Synthesis of Orally Bioavailable Piperazine Substituted 4(1H)Quinolones With Potent Antimalarial Activity: StructureActivity and StructureProperty Relationship Studies

Synthesis and Structure Activity Relationship of Some Indole Derivatives as Potential Anti-Inflammatory Agents

Structure-Activity Relationship of Potent Photo-Switchable Neuromuscular Inhibitors

Discovery, Synthesis, and in Vivo Activity of a New Class of Pyrazoloquinazolines as Selective Inhibitors of Aurora B Kinase

Synthesis and Pharmacological Characterization of Potent, Selective, and Orally Bioavailable Isoindoline Class Dipeptidyl Peptidase IV Inhibitors

Structure–activity Relationship Study of Acridine Analogs as Haspin and DYRK2 Kinase Inhibitors

Synthesis of Novel Naphthalene COX Inhibitors for Anti-Inflammatory Activity

Synthesis, Antibacterial and Anti-Mrsa Activity, in Vivo Toxicity and a Structure–activity Relationship Study of a Quinoline Thiourea