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12 articles for XM Wang


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

PMID
Data
Article Title
Organization
Modification of N-(6-(2-methoxy-3-(4-fluorophenylsulfonamido)pyridin-5-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-yl)acetamide as PI3Ks inhibitor by replacement of the acetamide group with alkylurea.EBI
Xi'An Jiaotong University
Synthesis and antitumor activities evaluation of m-(4-morpholinoquinazolin-2-yl)benzamides in vitro and in vivo.EBI
Xi'An Jiaotong University
Design, synthesis and antiproliferative activity evaluation of m-(4-morpholinyl-1,3,5-triazin-2-yl)benzamides in vitro.EBI
Xi'An Jiaotong University
Synthesis, biological evaluation and molecular docking studies of flavone and isoflavone derivatives as a novel class of KSP (kinesin spindle protein) inhibitors.EBI
Nanjing University
Synthesis and antitumor activity of 1,3,4-oxadiazole possessing 1,4-benzodioxan moiety as a novel class of potent methionine aminopeptidase type II inhibitors.EBI
Nanjing University
Design, synthesis and biological evaluation of pyrazolyl-thiazolinone derivatives as potential EGFR and HER-2 kinase inhibitors.EBI
Nanjing University
Design, synthesis and biological evaluation of N-phenylsulfonylnicotinamide derivatives as novel antitumor inhibitors.EBI
Nanjing University
Oxadiazole derivatives containing 1,4-benzodioxan as potential immunosuppressive agents against RAW264.7 cells.EBI
Nanjing University
Discovery and development of novel rhodanine derivatives targeting enoyl-acyl carrier protein reductase.EBI
Nanjing University
Design, synthesis and biological evaluation of benzoylacrylic acid shikonin ester derivatives as irreversible dual inhibitors of tubulin and EGFR.EBI
Nanjing University
Substituted indazoles useful for treatment and prevention of allergic and/or inflammatory diseases in animalsBDB
Bayer Pharma Aktiengesellschaft
Characterization of the CHK1 allosteric inhibitor binding site.BDB
Pfizer