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19 articles for thisTarget


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

PMID
Data
Article Title
Organization
Piceatannol, a natural trans-stilbene compound, inhibits human glyoxalase I.EBI
Tokyo University of Science
Pseudodeflectusin, a novel isochroman derivative from Aspergillus pseudodeflectus a parasite of the sea weed, Sargassum fusiform, as a selective human cancer cytotoxin.EBI
Tokyo University of Science
Ridaifen B, a tamoxifen derivative, directly binds to Grb10 interacting GYF protein 2.EBI
Tokyo University of Science
Transport of the dopamine D2 agonist pramipexole by rat organic cation transporters OCT1 and OCT2 in kidney.EBI
Tokyo University of Science
The antitumor agent doxorubicin binds to Fanconi anemia group F protein.EBI
Tokyo University of Science
1-deoxyrubralactone, a novel specific inhibitor of families X and Y of eukaryotic DNA polymerases from a fungal strain derived from sea algae.EBI
Tokyo University of Science
Camptothecin (CPT) directly binds to human heterogeneous nuclear ribonucleoprotein A1 (hnRNP A1) and inhibits the hnRNP A1/topoisomerase I interaction.EBI
Tokyo University of Science
Discovery of a new type inhibitor of human glyoxalase I by myricetin-based 4-point pharmacophore.EBI
Tokyo University of Science
DR396, an apoptotic DNase¿ inhibitor, attenuates high mobility group box 1 release from apoptotic cells.EBI
Tokyo University of Science
Delphinidin, a dietary anthocyanidin in berry fruits, inhibits human glyoxalase I.EBI
Tokyo University of Science
Podophyllotoxin directly binds a hinge domain in E2 of HPV and inhibits an E2/E7 interaction in vitro.EBI
Tokyo University of Science
Structure-based discovery of a novel non-peptidic small molecular inhibitor of caspase-3.EBI
Tokyo University of Science
Novel azaphilones, kasanosins A and B, which are specific inhibitors of eukaryotic DNA polymerases beta and lambda from Talaromyces sp.EBI
Tokyo University of Science
Structure-activity relationship of human GLO I inhibitory natural flavonoids and their growth inhibitory effects.EBI
Tokyo University of Science
Fine-tuning of nitrogen-containing bisphosphonate esters that potently induce degradation of HMG-CoA reductase.EBI
Tokyo University of Science
Structure-activity relationships of untenone A and its derivatives for inhibition of DNA polymerases.EBI
Tokyo University of Science
Addition of hydrophobic side chains improve the apoptosis inducibility of the human glyoxalase I inhibitor, TLSC702.EBI
Tokyo University of Science
Biotinylated lithocholic acids for affinity chromatography of mammalian DNA polymerases alpha and beta.EBI
Tokyo University of Science
Structural insights into the active site of poly(ADP-ribose) glycohydrolase using docking modes of 6-hydroxy-3H-xanthen-3-one derivative inhibitors.EBI
Tokyo University of Science