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Article Title

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Inhibition of the Aldehyde Dehydrogenase 1/2 Family by Psoralen and Coumarin Derivatives.

Indiana University School Of Medicine

Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors.

Indiana University

Development of selective inhibitors for aldehyde dehydrogenases based on substituted indole-2,3-diones.

Indiana University School Of Medicine

Structure-activity relationship studies and biological characterization of human NAD(+)-dependent 15-hydroxyprostaglandin dehydrogenase inhibitors.

National Center For Advancing Translational Sciences

Aldehyde dehydrogenase inhibitors: alpha,beta-acetylenic N-substituted aminothiolesters are reversible growth inhibitors of normal epithelial but irreversible apoptogens for cancer epithelial cells from human prostate in culture.

Claude Bernard University Lyon 1

Discovery of benzimidazole derivatives as potent and selective aldehyde dehydrogenase 1A1 (ALDH1A1) inhibitors with glucose consumption improving activity.

China Pharmaceutical University

Development of new disulfiram analogues as ALDH1a1-selective inhibitors.

Umm Al-Qura University

Development of 2,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one inhibitors of aldehyde dehydrogenase 1A (ALDH1A) as potential adjuncts to ovarian cancer chemotherapy.

University Of Michigan

Discovery of 5-(3-Chlorophenylamino)benzo[

Southeast University

Design, synthesis characterization and biological evaluation of novel multi-isoform ALDH inhibitors as potential anticancer agents.

The Pennsylvania State University College Of Medicine

Progress in the Field of Aldehyde Dehydrogenase Inhibitors: Novel Imidazo[1,2-

University Of Pisa

Discovery of coumarin-based selective aldehyde dehydrogenase 1A1 inhibitors with glucose metabolism improving activity.

China Pharmaceutical University

Imidazo[1,2-

University Of Pisa

Structure-Based Optimization of a Novel Class of Aldehyde Dehydrogenase 1A (ALDH1A) Subfamily-Selective Inhibitors as Potential Adjuncts to Ovarian Cancer Chemotherapy.

Indiana University School Of Medicine

Discovery of Orally Bioavailable, Quinoline-Based Aldehyde Dehydrogenase 1A1 (ALDH1A1) Inhibitors with Potent Cellular Activity.

National Center For Advancing Translational Sciences