Kuo-Long Yu

发表

A Chemical Switch Regulates Fibrate Specificity for Peroxisome Proliferator-activated Receptor α (PPARα) VersusLiver X Receptor*

K. Bramlett, W. Chin, J. Mccowan, 2003, The Journal of Biological Chemistry.

Targeting a binding pocket within the trimer-of-hairpins: small-molecule inhibition of viral fusion.

N. Meanwell, D. Langley, C. Cianci, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Retinoic acid receptor β,γ-selective ligands : Synthesis and biological activity of 6-substituted 2-naphthoic acid retinoids

J. Starrett, D. Tortolani, P. Reczek, 1996 .

Novel 3-aryl indoles as progesterone receptor antagonists for uterine fibroids.

A. Geiser, T. I. Richardson, J. Dodge, 2011, ACS medicinal chemistry letters.

Respiratory syncytial virus fusion inhibitors. Part 6: an examination of the effect of structural variation of the benzimidazol-2-one heterocycle moiety.

N. Meanwell, D. Langley, I. Medina, 2007, Bioorganic & medicinal chemistry letters.

Respiratory syncytial virus fusion inhibitors. Part 5: Optimization of benzimidazole substitution patterns towards derivatives with improved activity.

N. Meanwell, D. Langley, C. Cianci, 2007, Bioorganic & medicinal chemistry letters.

Respiratory syncytial virus fusion inhibitors. Part 3: Water-soluble benzimidazol-2-one derivatives with antiviral activity in vivo.

N. Meanwell, I. Medina, C. Cianci, 2006, Bioorganic & medicinal chemistry letters.

Respiratory syncytial virus inhibitors. Part 2: Benzimidazol-2-one derivatives.

N. Meanwell, C. Cianci, M. Krystal, 2004, Bioorganic & medicinal chemistry letters.

Fundamental structure-activity relationships associated with a new structural class of respiratory syncytial virus inhibitor.

N. Meanwell, C. Cianci, M. Krystal, 2003, Bioorganic & medicinal chemistry letters.

Development of a photoaffinity label for respiratory syncytial virus inhibitors

N. Meanwell, P. Williams, C. Cianci, 2003 .

Structure-activity relationships for a series of thiobenzamide influenza fusion inhibitors derived from 1,3,3-trimethyl-5-hydroxy-cyclohexylmethylamine.

N. Meanwell, C. Cianci, M. Krystal, 2002, Bioorganic & medicinal chemistry letters.

Carbohydrate-derived partners display remarkably high stereoselectivity in aldol coupling reactions

S. Handa, Kuo-Long Yu, B. Fraser-Reid, 1991 .

Respiratory syncytial virus fusion inhibitors. Part 4: optimization for oral bioavailability.

A. Marino, N. Meanwell, I. Medina, 2007, Bioorganic & medicinal chemistry letters.

Structural modifications of 6-naphthalene-2-carboxylate retinoids

J. Starrett, P. Reczek, J. Ostrowski, 1996 .

A novel reagent for the synthesis of myo-inositol phosphates: N,N-diisopropyl dibenzyl phosphoramidite

Kuo-Long Yu, B. Fraser-Reid, Kuo-long Yu, 1988 .

Synthesis of 1,3-diamino-2-hydroxypropane derivatives as pseudosymmetric HIV protease inhibitors

W. Harte, Kuo-Long Yu, M. Mansuri, 1993 .

Infrared and Nuclear Magnetic Resonance Spectroscopic Study of Secondary Amide Hydrogen Bonding in Benzoyl PABA Derivatives (Retinoids)

R. Dalterio, Kuo-Long Yu, X. Huang, 2007, Applied spectroscopy.

Oral Efficacy of a Respiratory Syncytial Virus Inhibitor in Rodent Models of Infection

N. Meanwell, I. Medina, C. Cianci, 2004, Antimicrobial Agents and Chemotherapy.

Orally Active Fusion Inhibitor of Respiratory Syncytial Virus

N. Meanwell, I. Medina, C. Cianci, 2004, Antimicrobial Agents and Chemotherapy.