42 articles for thisTarget

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

PMID	Data	Article Title	Organization
32366720	53	Identification of Antiviral Drug Candidates against SARS-CoV-2 from FDA-Approved Drugs.	Institut Pasteur Korea
27479541	24	Design, synthesis and biological evaluation of coumarin derivatives as novel acetylcholinesterase inhibitors that attenuate H2O2-induced apoptosis in SH-SY5Y cells.	Shenyang Pharmaceutical University
7908055	157	Binding of typical and atypical antipsychotic agents to 5-hydroxytryptamine-6 and 5-hydroxytryptamine-7 receptors.	Case Western Reserve University
19519743	6	Potent triazolothione inhibitor of heat-shock protein-90.	Bayer Healthcare
18722772	105	Discovery of a novel class of PPARdelta partial agonists.	Gsk
19168351	18	Novel potent inhibitors of hepatitis C virus (HCV) NS3 protease with cyclic sulfonyl P3 cappings.	Schering-Plough Research Institute
19007109	37	Novel Naphthalene-N-sulfonyl-d-glutamic Acid Derivatives as Inhibitors of MurD, a Key Peptidoglycan Biosynthesis Enzyme.	Lek Pharmaceuticals
17488003	32	Rationally designed high-affinity 2-amino-6-halopurine heat shock protein 90 inhibitors that exhibit potent antitumor activity.	Biogen Idec
12825935	54	Estrogen receptor modulators: identification and structure-activity relationships of potent ERalpha-selective tetrahydroisoquinoline ligands.	Novartis Pharmaceuticals
17113558	21	Binding thermodynamics of substituted diaminopyrimidine renin inhibitors.	Pfizer
15084132	88	Carbonic anhydrase inhibitors. Design of selective, membrane-impermeant inhibitors targeting the human tumor-associated isozyme IX.	Canadian Institutes of Health Research
17004721	49	Discovery of (1R,5S)-N-[3-amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]-3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (SCH 503034), a selective, potent, orally bioavailable hepatitis C virus NS3 protease inhibitor	Schering-Plough Research Institute
11572683	11	Fluoroaromatic-fluoroaromatic interactions between inhibitors bound in the crystal lattice of human carbonic anhydrase II.	University of Pennsylvania
8691434	25	Structure-based design of novel HIV protease inhibitors: sulfonamide-containing 4-hydroxycoumarins and 4-hydroxy-2-pyrones as potent non-peptidic inhibitors.	Upjohn