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The Journal of Organic Chemistry|October 23, 2004
Design and efficient synthesis of 2 alpha-(omega-hydroxyalkoxy)-1 alpha,25-dihydroxyvitamin D3 Analogues, including 2-epi-ED-71 and their 20-epimers with HL-60 cell differentiation activityNozomi Saito, Yoshitomo Suhara, Masaaki Kurihara, et al.Bioorganic & Medicinal Chemistry|October 27, 2005
Structural basis for DNA-cleaving activity of resveratrol in the presence of Cu(II)Kiyoshi Fukuhara, Maki Nagakawa, Ikuo Nakanishi, et al.Chemical Research in Toxicology|April 16, 2003
A planar catechin analogue as a promising antioxidant with reduced prooxidant activityKiyoshi Fukuhara, Ikuo Nakanishi, Tomokazu Shimada, et al.Bioorganic & Medicinal Chemistry|January 14, 2011
Synthesis and biological activity of optically active NCL-1, a lysine-specific demethylase 1 selective inhibitorDaisuke Ogasawara, Takayoshi Suzuki, Koshiki Mino, et al.Bioorganic & Medicinal Chemistry|July 14, 2016
Design, synthesis, and evaluation of Trolox-conjugated amyloid-β C-terminal peptides for therapeutic intervention in an in vitro model of Alzheimer's diseaseTakuya Arai, Akiko Ohno, Mori Kazunori, et al.Journal of Medicinal Chemistry|November 15, 2008
Identification of G protein-coupled receptor 120-selective agonists derived from PPARgamma agonistsTakayoshi Suzuki, Sou-Ichi Igari, Akira Hirasawa, et al.Oncotarget|December 19, 2012
KDM1 is a novel therapeutic target for the treatment of gliomasGangadhara R Sareddy, Binoj C Nair, Samaya K Krishnan, et al.Journal of the American Chemical Society|May 18, 2006
Planar catechin analogues with alkyl side chains: a potent antioxidant and an alpha-glucosidase inhibitorWataru Hakamata, Ikuo Nakanishi, Yu Masuda, et al.Plos One|August 2, 2014
Histone deacetylase inhibitor valproic acid promotes the differentiation of human induced pluripotent stem cells into hepatocyte-like cellsYuki Kondo, Takahiro Iwao, Sachimi Yoshihashi, et al.Journal of Medicinal Chemistry|November 3, 2012
Rapid discovery of highly potent and selective inhibitors of histone deacetylase 8 using click chemistry to generate candidate librariesTakayoshi Suzuki, Yosuke Ota, Masaki Ri, et al.Pageof 12