16 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Syntheses and antitumor activity of cis-restricted combretastatins: 5-membered heterocyclic analogues.

Ajinomoto
Interaction Analysis of FABP4 Inhibitors by X-ray Crystallography and Fragment Molecular Orbital Analysis.

Ajinomoto
Syntheses of novel antitumor dihydroxanthone derivatives with inhibitory activity against DNA topoisomerase II.

Ajinomoto
Synthesis and evaluation of isoxazole derivatives as lysophosphatidic acid (LPA) antagonists.

Ajinomoto
Rational design, synthesis, and structure-activity relationships of novel factor Xa inhibitors: (2-substituted-4-amidinophenyl)pyruvic and -propionic acids.

Ajinomoto
Design, synthesis and evaluation of unnatural peptides as T1R2/T1R3 PAMs.

Ajinomoto
Unnatural Tripeptides as Potent Positive Allosteric Modulators of T1R2/T1R3.

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.

Ajinomoto
Structure-activity relationship study of 1,4-dihydropyridine derivatives blocking N-type calcium channels.

Ajinomoto
Novel combretastatin analogues effective against murine solid tumors: design and structure-activity relationships.

Ajinomoto
Therapeutic agents

Astrazeneca
2-pyridyloxy-4-nitrile orexin receptor antagonists

TBA
Allosteric competitive inhibitors of the glucose-1-phosphate thymidylyltransferase (RmlA) from Pseudomonas aeruginosa.

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.

The Scripps Research Institute
Pharmacological profile of TP-680, a new cholecystokininA receptor antagonist.

University of Occupational and Environmental Health
A neoceptor approach to unraveling microscopic interactions between the human A2A adenosine receptor and its agonists.

National Institutes of Health