PMID

Data

Article Title

Organization

Quantitative structure-activity relationships of N2-phenylguanines as inhibitors of herpes simplex virus thymidine kinases.

University of Massachusetts Medical School

Design, synthesis, and biological evaluation of tetrazole analogs of Cl-amidine as protein arginine deiminase inhibitors.

University of Massachusetts Medical School

Cannabidiol (CBD) and its analogs: a review of their effects on inflammation.

University of Massachusetts Medical School

A small molecule inhibitor of fungal histone acetyltransferase Rtt109.

University of Massachusetts Medical School

Design and synthesis of a novel peptidomimetic inhibitor of HIV-1 Tat-TAR interactions: squaryldiamide as a new potential bioisostere of unsubstituted guanidine.

University of Massachusetts Medical School

Fluorogenic probes for monitoring peptide binding to class II MHC proteins in living cells.

University of Massachusetts Medical School

The Ascension of Targeted Covalent Inhibitors.

University of Massachusetts Medical School

Discovery of Quinoxaline-Based P1-P3 Macrocyclic NS3/4A Protease Inhibitors with Potent Activity against Drug-Resistant Hepatitis C Virus Variants.

University of Massachusetts Medical School

Structural Analysis of Potent Hybrid HIV-1 Protease Inhibitors Containing Bis-tetrahydrofuran in a Pseudosymmetric Dipeptide Isostere.

University of Massachusetts Medical School

HIV-1 Protease Inhibitors Incorporating Stereochemically Defined P2' Ligands To Optimize Hydrogen Bonding in the Substrate Envelope.

University of Massachusetts Medical School

Synthesis, properties, and pharmacokinetic studies of N2-phenylguanine derivatives as inhibitors of herpes simplex virus thymidine kinases.

University of Massachusetts Medical School

Structure-based design, synthesis, and structure-activity relationship studies of HIV-1 protease inhibitors incorporating phenyloxazolidinones.

University of Massachusetts Medical School

Quinoxaline-Based Linear HCV NS3/4A Protease Inhibitors Exhibit Potent Activity against Drug Resistant Variants.

University of Massachusetts Medical School

Development of a Selective Inhibitor of Protein Arginine Deiminase 2.

University of Massachusetts Medical School

Structure-activity relationships of N2-substituted guanines as inhibitors of HSV1 and HSV2 thymidine kinases.

University of Massachusetts Medical School

Aza-heteroaryl compounds as PI3K-gamma inhibitors

Incyte

Cloning of cDNA sequences encoding human alpha 2 and alpha 3 gamma-aminobutyric acidA receptor subunits and characterization of the benzodiazepine pharmacology of recombinant alpha 1-, alpha 2-, alpha 3-, and alpha 5-containing human gamma-aminobutyric acidA receptors.

Merck Sharp & Dohme Research Laboratories

Synthesis of 1,7-annulated indoles and their applications in the studies of cyclin dependent kinase inhibitors.

Eli Lilly