Druggable Lipid Signaling Pathways
portes grátis
Druggable Lipid Signaling Pathways
Kihara, Yasuyuki
Springer Nature Switzerland AG
09/2021
260
Mole
Inglês
9783030506230
15 a 20 dias
609
Descrição não disponível.
Preface.- Introduction of Druggable Lipid Signaling Pathway.- Biosynthetic Enzymes of Membrane Glycerophospholipid Diversity as Therapeutic Targets for Drug Development.- Druggable Prostanoid Pathway.- Targeting Leukotrienes as a Therapeutic Strategy to Prevent Comorbidities Associated with Metabolic Stress.- Epoxy Fatty Acids are Promising Targets for Treatment of Pain, Cardiovascular Disease and Other Indications Characterized by Mitochondrial Dysfunction, Endoplasmic Stress and Inflammation.- Druggable Sphingolipid Pathway.- Druggable Lysophospholipid Pathway.- Druggable targets in endocannabinoid signaling.- Drugging the phosphoinositide 3-kinase (PI3K) and phosphatidylinositol 4-kinase (PI4K) family of enzymes for treatment of cancer, immune disorders, and viral/parasitic infections.- Druggable Lipid GPCRs: Past, Present, and Prospects.
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lipids;GPCR;drug discovery;disease;translational research
Preface.- Introduction of Druggable Lipid Signaling Pathway.- Biosynthetic Enzymes of Membrane Glycerophospholipid Diversity as Therapeutic Targets for Drug Development.- Druggable Prostanoid Pathway.- Targeting Leukotrienes as a Therapeutic Strategy to Prevent Comorbidities Associated with Metabolic Stress.- Epoxy Fatty Acids are Promising Targets for Treatment of Pain, Cardiovascular Disease and Other Indications Characterized by Mitochondrial Dysfunction, Endoplasmic Stress and Inflammation.- Druggable Sphingolipid Pathway.- Druggable Lysophospholipid Pathway.- Druggable targets in endocannabinoid signaling.- Drugging the phosphoinositide 3-kinase (PI3K) and phosphatidylinositol 4-kinase (PI4K) family of enzymes for treatment of cancer, immune disorders, and viral/parasitic infections.- Druggable Lipid GPCRs: Past, Present, and Prospects.
Este título pertence ao(s) Especialidade(s) indicados(s). Para ver outros títulos clique no Especialidade desejado.
