PMID

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Discovery of Antimalarial Azetidine-2-carbonitriles That Inhibit

Harvard University

Discovery of 8-Membered Ring Sulfonamides as Inhibitors of Oncogenic Mutant Isocitrate Dehydrogenase 1.

Harvard University

OpenGrowth: An Automated and Rational Algorithm for Finding New Protein Ligands.

Harvard University

Three-dimensional quantitative structure-activity relationships from molecular similarity matrices and genetic neural networks. 2. Applications.

Harvard University

Genetic neural networks for quantitative structure-activity relationships: improvements and application of benzodiazepine affinity for benzodiazepine/GABAA receptors.

Harvard University

Structure of human cytidine deaminase bound to a potent inhibitor.

Harvard University

2,6-Dimethyltyrosine analogues of a stereodiversified ligand library: highly potent, selective, non-peptidic mu opioid receptor agonists.

Harvard University

Multiple copy simultaneous search and construction of ligands in binding sites: application to inhibitors of HIV-1 aspartic proteinase.

Harvard University

Microarray-based method for monitoring yeast overexpression strains reveals small-molecule targets in TOR pathway.

Harvard University

Molecular basis of cyclin-CDK-CKI regulation by reversible binding of an inositol pyrophosphate.

Harvard University

Design and Development of IKZF2 and CK1α Dual Degraders.

Harvard University

Development of a highly potent and selective degrader of LRRK2.

Harvard University

Potent Uncompetitive Inhibitors of Nicotinamide

Harvard University

Discovery of a Cyclic Choline Analog That Inhibits Anaerobic Choline Metabolism by Human Gut Bacteria.

Harvard University

Identification of two hydrophobic patches in the active-site cavity of human carbonic anhydrase II by solution-phase and solid-state studies and their use in the development of tight-binding inhibitors.

Harvard University

SMall Molecule Growth 2001 (SMoG2001): an improved knowledge-based scoring function for protein-ligand interactions.

Harvard University

Heterocycle-substituted pyridyl benzothiophenes as kinase inhibitors

Allergan

A new screening assay for allosteric inhibitors of cSrc.

Chemical Genomics Centre of The Max Planck Society