Zobrazeno 41 - 50
of 69
pro vyhledávání: '"Ronald L. Hanson"'
Autor:
Yande Huang, Haiying Zhang, Mingshe Zhu, W. Griffith Humphreys, Peter T. W. Cheng, Nelly Aranibar, Ronald L. Hanson, Donglu Zhang, Arun Swaminathan, Samuel J. Bonacorsi, Shung Wu
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 34(2)
Muraglitazar (Pargluva), a dual alpha/gamma peroxisome proliferator-activated receptor activator, is currently in clinical development for treatment of type 2 diabetes. This study describes the structural elucidation of the human oxidative metabolite
Autor:
Vikram Roongta, W. Griffith Humphreys, Mingshe Zhu, Yue-Zhong Shu, Aberra Fura, Ronald L. Hanson
Publikováno v:
ChemInform. 35
Bristol Myers Squibb, Pharmaceutical Research Institute, P.O. Box 5400, Princeton, New Jersey 08534, Bristol-Myers Squibb, Pharmaceutical Research Institute, 5 Research Parkway, Wallingford, Connecticut 06492, Bristol Myers Squibb, Pharmaceutical Res
Publikováno v:
Biotechnology and applied biochemistry. 39(Pt 2)
6-alpha-Hydroxy-7-deoxy-10-deacetylbaccatin-III is an intermediate that is potentially useful for synthesis of analogues of paclitaxel. Screening of microbial strains identified an enzyme activity in Nocardioides luteus SC 13912 (A.T.C.C. 55426) whic
Autor:
Vadim A. Soloshonok, Kunisuke Izawa, Richard F. W. Jackson, Alessandro Dondoni, Alessandro Massi, Takeo Kawabata, Yasufumi Ohfune, Kazuhiko Sakaguchi, Tetsuro Shinada, Hisanori Ueki, Trevor K. Ellis, Kazumi Okuro, Yasuhiro Saka, Ikuhiro Suzuki, Masaru Mitsuda, Masakatsu Shibasaki, Motomu Kanai, Keiji Maruoka, Yasuhiro Yamashita, Shū Kobayashi, Uli Kazmaier, Takashi Ooi, Nicklas Selander, Kálmán J. Szabó, Hideo Shimizu, Izuru Nagasaki, Noboru Sayo, Takao Saito, Yasumasa Hamada, Kazuishi Makino, David J. Ager, Laurent Lefort, Johannes G. de Vries, Rafael Chinchílla, Carmen Nájera, Jianfeng Hang, Yutaka Ishii, Yoshiro Furukawa, Li Deng, David B. Berkowitz, Kannan R. Karukurichi, Roberto de la Salud-Bea, Gourhari Maiti, Jill M. McFadden, Michelle L. Morris, Ronald L. Hanson, Ian V. Archer, S. Alison Arnold, Reuben Carr, Ian G. Fotheringham, Robert E. Speight, Paul P. Taylor, Takahiro Ohishi, Masahiko Yamada, Masanobu Sugawara, Mari Hara Yasuda, Makoto Ueda, Kazuya Okano, Hisaaki Mihara, Nobuyoshi Esaki, S. Verseck, U. Becker, K. Doderer, S. Oβwald, W
Autor:
Ramesh N. Patel, Ronald L. Hanson
Publikováno v:
ACS Symposium Series ISBN: 9780841236790
Applied Biocatalysis in Specialty Chemicals and Pharmaceuticals
Applied Biocatalysis in Specialty Chemicals and Pharmaceuticals
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe3d084694e0a8fa6a08de1e37e2f7a1
https://doi.org/10.1021/bk-2001-0776.ch015
https://doi.org/10.1021/bk-2001-0776.ch015
Autor:
Zhongping Shi, David B. Brzozowski, Jeffrey M. Howell, Jeffrey T. North, Annie Pullockaran, Thomas P. Kissick, Ramesh N. Patel, Ronald L. Hanson, Amit Banerjee, David R. Kronenthal, Janak Singh, Junying Fan, Richard H. Mueller, Michael A. Montana, Susan C Durand
Publikováno v:
Bioorganicmedicinal chemistry. 8(12)
Synthesis of lobucavir prodrug, L-valine, [(1S,2R,3R)-3-(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)-2-(hydroxymethyl) cyclobutyl]methyl ester monohydrochloride (BMS 233866), requires regioselective coupling of one of the two hydroxyl groups of lobucavi
Autor:
Ian S. Young, Matthew W. Haley, Annie Tam, Steven A. Tymonko, Zhongmin Xu, Ronald L. Hanson, Animesh Goswami
Publikováno v:
Organic Process Research & Development; Oct2015, Vol. 19 Issue 10, p1360-1368, 9p
Autor:
Fiona H. Rodgers, David W. Rice, Timothy J. Stillman, Stephen R. Ashford, Patrick J. Baker, Ronald L. Hanson, Andrew P. Turnbull
Publikováno v:
Journal of molecular biology. 236(2)
The NAD(+)-dependent leucine dehydrogenase from Bacillus sphaericus has been crystallized by the hanging drop method of vapour diffusion, using ammonium sulphate as the precipitant. The crystals belong to the tetragonal system and are in space group
Publikováno v:
Applied microbiology and biotechnology. 37(5)
Biotransformations were developed to oxidize N epsilon-carbobenzoxy(CBZ)-L-lysine and to reduce the product keto acid to L-CBZ-oxylysine. Lysyl oxidase (L-lysine: O2 oxidoreductase, EC 1.4.3.14) from Trichoderma viride was relatively specific for L-l