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Journal of the American Chemical Society|May 15, 2009
Photoinduced nitric oxide release from a hindered nitrobenzene derivative by two-photon excitationKazuhiro Hishikawa, Hidehiko Nakagawa, Toshiaki Furuta, et al.
Chemical Communications (Cambridge, England)|April 16, 2010
Alternative photoinduced release of HNO or NO from an acyl nitroso compound, depending on environmental polarityKazuya Matsuo, Hidehiko Nakagawa, Yusuke Adachi, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2014
Visible light-induced nitric oxide release from a novel nitrobenzene derivative cross-conjugated with a coumarin fluorophoreKai Kitamura, Naoya Ieda, Kazuhiro Hishikawa, et al.
Bioengineering (Basel, Switzerland)|July 29, 2025
Therapeutic Potential of Local Application of Fibroblast Growth Factor-2 to Periodontal Defects in a Preclinical Osteoporosis ModelShinta Mori, Sho Mano, Naoki Miyata, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2003
Novel histone deacetylase inhibitors: design, synthesis, enzyme inhibition, and binding mode study of SAHA-based non-hydroxamatesTakayoshi Suzuki, Yuki Nagano, Azusa Matsuura, et al.
Bioorganic & Medicinal Chemistry Letters|May 20, 2004
Thiol-based SAHA analogues as potent histone deacetylase inhibitorsTakayoshi Suzuki, Akiyasu Kouketsu, Azusa Matsuura, et al.
Chemical & Pharmaceutical Bulletin|July 3, 2007
Synthesis and evaluation of 2-Nonylaminopyridine derivatives as PPAR ligandsShinya Usui, Hiroki Fujieda, Takayoshi Suzuki, et al.
Journal of Medicinal Chemistry|August 4, 2006
Highly potent and selective histone deacetylase 6 inhibitors designed based on a small-molecular substrateTakayoshi Suzuki, Akiyasu Kouketsu, Yukihiro Itoh, et al.
Drug Metabolism and Pharmacokinetics|February 3, 2020
Clinical study designs and patient selection methods based on genomic biomarkers: Points-to-consider documentsMasahiro Tohkin, Yoshiro Saito, Satomi Yagi, et al.
Journal of Medicinal Chemistry|February 18, 2005
Novel inhibitors of human histone deacetylases: design, synthesis, enzyme inhibition, and cancer cell growth inhibition of SAHA-based non-hydroxamatesTakayoshi Suzuki, Yuki Nagano, Akiyasu Kouketsu, et al.
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