19 articles for thisTarget
              
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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