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12 articles for MJ Costanzo


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
2-Substituted 1-azabicycloalkanes, a new class of non-opiate antinociceptive agents.EBI
R. W. Johnson Pharmaceutical Research Institute
Inhibitors of proteases and amide hydrolases that employ an alpha-ketoheterocycle as a key enabling functionality.EBI
Johnson & Johnson Pharmaceutical Research & Development
Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives.EBI
Johnson & Johnson Pharmaceutical Research & Development
Comparison of sulfamate and sulfamide groups for the inhibition of carbonic anhydrase-II by using topiramate as a structural platform.EBI
Johnson & Johnson Pharmaceutical Research & Development
Potent, small-molecule inhibitors of human mast cell tryptase. Antiasthmatic action of a dipeptide-based transition-state analogue containing a benzothiazole ketone.EBI
Johnson & Johnson Pharmaceutical Research & Development
Potent thrombin inhibitors that probe the S1 subsite: tripeptide transition state analogues based on a heterocycle-activated carbonyl group.EBI
R. W. Johnson Pharmaceutical Research Institute
Pyrroloisoquinoline antidepressants. 3. A focus on serotonin.EBI
Mcneil Pharmaceutical
Pyrroloisoquinoline antidepressants. 2. In-depth exploration of structure-activity relationships.EBI
TBA
 
Solid-phase parallel synthesis applied to lead optimization: Discovery of potent analogues of the GPIIb/IIIa antagonist RWJ-50042EBI
TBA
Potent, orally active GPIIb/IIIa antagonists containing a nipecotic acid subunit. Structure-activity studies leading to the discovery of RWJ-53308.EBI
The R. W. Johnson Pharmaceutical Research Institute
USE OF PRIDOPIDINE AND ANALOGS FOR TREATING RETT SYNDROMEBDB
Prilenia Neurotherapeutics
5-aminopyrazole-4-carboxamide inhibitors of CDPK1 from T. gondii and C. parvumBDB
University of Washington Through Its Center For Commercialization