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16 articles for thisTarget


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

PMID
Data
Article Title
Organization
Syntheses and antitumor activity of cis-restricted combretastatins: 5-membered heterocyclic analogues.EBI
Ajinomoto
Interaction Analysis of FABP4 Inhibitors by X-ray Crystallography and Fragment Molecular Orbital Analysis.EBI
Ajinomoto
Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II.EBI
Ajinomoto
Synthesis and evaluation of isoxazole derivatives as lysophosphatidic acid (LPA) antagonists.EBI
Ajinomoto
Rational design, synthesis, and structure-activity relationships of novel factor Xa inhibitors: (2-substituted-4-amidinophenyl)pyruvic and -propionic acids.EBI
Ajinomoto
Design, synthesis and evaluation of unnatural peptides as T1R2/T1R3 PAMs.EBI
Ajinomoto
Unnatural Tripeptides as Potent Positive Allosteric Modulators of T1R2/T1R3.EBI
Ajinomoto
The structure-activity relationship study on 2-, 5-, and 6-position of the water soluble 1,4-dihydropyridine derivatives blocking N-type calcium channels.EBI
Ajinomoto
Structure-activity relationship study of 1,4-dihydropyridine derivatives blocking N-type calcium channels.EBI
Ajinomoto
Novel combretastatin analogues effective against murine solid tumors: design and structure-activity relationships.EBI
Ajinomoto
Therapeutic agentsBDB
Astrazeneca
2-pyridyloxy-4-nitrile orexin receptor antagonistsBDB
TBA
Allosteric competitive inhibitors of the glucose-1-phosphate thymidylyltransferase (RmlA) from Pseudomonas aeruginosa.BDB
University of St. Andrews
Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38.BDB
The Scripps Research Institute
Pharmacological profile of TP-680, a new cholecystokininA receptor antagonist.BDB
University of Occupational and Environmental Health
A neoceptor approach to unraveling microscopic interactions between the human A2A adenosine receptor and its agonists.BDB
National Institutes of Health