20 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
2-Amino-3-(phenylsulfanyl)norbornane-2-carboxylate: an appealing scaffold for the design of Rac1-Tiam1 protein-protein interaction inhibitors.

University of Milan
Structure-activity relationship of isoform selective inhibitors of Rac1/1b GTPase nucleotide binding.

Exonhit Therapeutics
Virtual screening approach for the identification of new Rac1 inhibitors.

University of Milan
Advances in the development of Rho GTPase inhibitors.

Shanghai Jiao Tong University
Targeting Small GTPases and Their Prenylation in Diabetes Mellitus.

Lodz University of Technology
Design, synthesis and biological evaluation of new carbazole derivatives as anti-cancer and anti-migratory agents.

University of Puerto Rico
Indazoles and use thereof

Purdue Pharma
Benzylamine derivatives

Kalvista Pharmceuticals
Piperidinone carboxamide azaindane CGRP receptor antagonists

Merck Sharp & Dohme
Pyridinecarboxamides as CXCR2 modulators

Syntrix Biosystems
Pyridine compounds

Daiichi Sankyo
3,3-difluoro-piperidine derivatives as NR2B NMDA receptor antagonists

Rugen Holdings (Cayman)
Substituted pyrrolo[3,4-e]indolizines, imidazo[1,2-a]pyrrolo[3,4-e]pyridines, pyrrolo[3,4-e][1,2,4]triazolo[1,5-a]pyridines and pyrrolo[3,4-e][1,2,4]triazolo[4,3-a]pyridines as positive allosteric modulators of muscarinic acetylcholine receptor M1

Vanderbilt University
Benzothiazole and benzisothiazole-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction

Vanderbilt University
Phosphatidylinositol 3-kinase inhibitors

Gilead Sciences
Novel aminophenyl benzamide-type histone deacetylase inhibitors with enhanced potency and selectivity.

Methylgene
2,4-diaminopyrimidine derivatives as potent growth hormone secretagogue receptor antagonists.

Abbott Laboratories
Discovery and pharmacological evaluation of growth hormone secretagogue receptor antagonists.

Abbott Laboratories
Synthesis and monoamine oxidase inhibitory activity of new pyridazine-, pyrimidine- and 1,2,4-triazine-containing tricyclic derivatives.

University of Bari
Tumor suppression by a rationally designed reversible inhibitor of methionine aminopeptidase-2.

Abbott Laboratories