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Drug Metabolism and Disposition: the Biological Fate of Chemicals|May 14, 2010
Furanocoumarin derivatives in Kampo extract medicines inhibit cytochrome P450 3A4 and P-glycoproteinKazunori Iwanaga, Manami Hayashi, Yukimi Hamahata, et al.Journal of Natural Products|August 4, 2007
Eremophilane sesquiterpenes from Ligularia macrophyllaQi Wang, Qing Mu, Makio Shibano, et al.Bioorganic & Medicinal Chemistry|May 11, 2010
New orally bioavailable 2-aminobenzamide-type histone deacetylase inhibitor possessing a (2-hydroxyethyl)(4-(thiophen-2-yl)benzyl)amino groupShingo Kiyokawa, Yoshiyuki Hirata, Yasuo Nagaoka, et al.Chemical & Pharmaceutical Bulletin|December 5, 2012
Divergent synthesis and evaluation of inhibitory activities against cyclooxygenases-1 and -2 of natural withasomnines and analoguesYoshihide Usami, Ryo Watanabe, Yuiko Fujino, et al.Journal of Natural Products|July 17, 2007
Filiasparosides A-D, cytotoxic steroidal saponins from the roots of Asparagus filicinusLi-Bo Zhou, Tzu-Hsuan Chen, Kenneth F Bastow, et al.Biological & Pharmaceutical Bulletin|July 6, 2005
Melanogenesis stimulation in murine b16 melanoma cells by umberiferae plant extracts and their coumarin constituentsHideaki Matsuda, Noriko Hirata, Yoshiko Kawaguchi, et al.Bioorganic & Medicinal Chemistry Letters|February 11, 2012
Anti-tumor activity of new orally bioavailable 2-amino-5-(thiophen-2-yl)benzamide-series histone deacetylase inhibitors, possessing an aqueous soluble functional group as a surface recognition domainYoshiyuki Hirata, Masahiko Hirata, Yasuyuki Kawaratani, et al.Bioorganic & Medicinal Chemistry|June 14, 2011
New microtubule polymerization inhibitors comprising a nitrooxymethylphenyl groupYasuyuki Kawaratani, Tomohiko Harada, Yoshiyuki Hirata, et al.Planta Medica|April 2, 2014
Synergistic antitumor effect of a combination of paclitaxel and carboplatin with nobiletin from Citrus depressa on non-small-cell lung cancer cell linesShinichi Uesato, Hirofumi Yamashita, Ryu Maeda, et al.Marine Drugs|April 25, 2020
Syntheses and Glycosidase Inhibitory Activities, and in Silico Docking Studies of Pericosine E Analogs Methoxy-Substituted at C6Yoshihide Usami, Megumi Higuchi, Koji Mizuki, et al.Pageof 5