PMID

Data

Article Title

Organization

Creation of Customized Bioactivity within a 14-Membered Macrolide Scaffold: Design, Synthesis, and Biological Evaluation Using a Family-18 Chitinase.

Kitasato University

NMR spectroscopy and computational analysis of interaction between Serratia marcescens chitinase B and a dipeptide derived from natural-product cyclopentapeptide chitinase inhibitor argifin.

Kitasato University

Computer-aided rational molecular design of argifin-derivatives with increased inhibitory activity against chitinase B from Serratia marcescens.

Kitasato University

Argifin; efficient solid phase total synthesis and evaluation of analogues of acyclic peptide.

Kitasato University

Computational analysis of the binding affinities of the natural-product cyclopentapeptides argifin and argadin to chitinase B from Serratia marcescens.

Kitasato University

An insight into the medicinal attributes of berberine derivatives: A review.

Isf College of Pharmacy

Fragment Linking Strategies for Structure-Based Drug Design.

Universit£

A Series of Compounds Bearing a Dipyrido-Pyrimidine Scaffold Acting as Novel Human and Insect Pest Chitinase Inhibitors.

Dalian University of Technology

Druggability Assessment of Targets Used in Kinetic Target-Guided Synthesis.

University of Groningen

The putative endocannabinoid transport blocker LY2183240 is a potent inhibitor of FAAH and several other brain serine hydrolases.

The Scripps Research Institute