7 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Design, synthesis, biological and structural evaluation of functionalized resveratrol analogues as inhibitors of quinone reductase 2.
Purdue University
A novel quantitative structure-activity relationship method to predict the affinities of MT3 melatonin binding site.
Lanzhou University
Dabigatran and dabigatran ethyl ester: potent inhibitors of ribosyldihydronicotinamide dehydrogenase (NQO2).
Caprotec Bioanalytics
Synthesis of novel¿¿3 receptor ligands via an unusual Knoevenagel condensation.
Moscow State University
Design, synthesis, and biological evaluation of resveratrol analogues as aromatase and quinone reductase 2 inhibitors for chemoprevention of cancer.
Purdue University