Author pages are created from data sourced from our academic publisher partnerships and public sources.
- Publications
- Influence
Small dipeptide-based HIV protease inhibitors containing the hydroxymethylcarbonyl isostere as an ideal transition-state mimic.
- Y. Kiso, H. Matsumoto, S. Mizumoto, T. Kimura, Y. Fujiwara, K. Akaji
- Chemistry, Medicine
- Biopolymers
- 1999
The human immunodeficiency virus (HIV) codes for an aspartic protease known to be essential for retroviral maturation and replication. HIV protease is formed from two identical 99 amino acid… Expand
An efficient route for the synthesis of methyl (−)-1,4a-dimethyl-5-oxodecahydronaphthalene-1-carboxylate by using baker’s yeast-catalyzed asymmetric reduction
- T. Katoh, S. Mizumoto, Masato Fudesaka, Masatoshi Takeo, T. Kajimoto, M. Node
- Chemistry
- 17 July 2006
Abstract Methyl (−)-1,4a-dimethyl-5-oxodecahydronaphthalene-1-carboxylate 1 , a key synthetic intermediate for the synthesis of terpenoids, was efficiently synthesized by using a baker’s… Expand
Inversion of Diastereoselectivity Depending on Substrate Concentration in Baker′s Yeast Catalyzed Reduction of σ-Symmetrical 1,3-Cyclopentadiones and 1,3-Cyclohexadiones.
- T. Katoh, S. Mizumoto, Masato Fudesaka, Yuki Nakashima, T. Kajimoto, M. Node
- Chemistry
- 12 December 2006
Inversion of diastereoselectivity depending on substrate concentration in baker's yeast catalyzed reduction of σ-symmetrical 1,3-cyclopentadiones and 1,3-cyclohexadiones
- T. Katoh, S. Mizumoto, Masato Fudesaka, Yuki Nakashima, T. Kajimoto, M. Node
- Chemistry
- 1 September 2006
Inversion of diastereoselectivity caused by a change in substrate concentration was first observed in baker's yeast catalyzed reduction of cr-symmetrical 2,2-dialkylated cyclopentan-1,3-diones 1,2… Expand
Asymmetric Synthesis of Methyl (-)-13-Oxo-15,16-dinorlabda-8(17),11E-dien-19-oate (IV), Methyl Ester of a Potent Suppressor Toward Carcinogenic Promotor (V).
- T. Katoh, S. Mizumoto, Masato Fudesaka, T. Kajimoto, M. Node
- Chemistry
- 20 February 2007
CCDC 610518: Experimental Crystal Structure Determination
- T. Katoh, S. Mizumoto, Masato Fudesaka, Masatoshi Takeo, Tetsuya Kajimoto, M. Node
- Materials Science
- 2007
Nouveau dérivé de nicotinamide ou sel de celui-ci
- Hideyasu Fujiwara, 藤原 秀安, +17 authors 山本 真理
- Chemistry
- 28 December 2011
L'invention concerne un compose et une composition pharmaceutique presentant une excellente activite inhibitrice de la Syk. Selon l'invention, on utilise un derive de nicotinamide represente par la… Expand
Asymmetric synthesis of methyl (-)-13-oxo-15,16-dinorlabda-8(17),11E-dien-19-oate, methyl ester of a potent suppressor toward carcinogenic promotor.
- T. Katoh, S. Mizumoto, Masato Fudesaka, T. Kajimoto, M. Node
- Chemistry, Medicine
- Chemical & pharmaceutical bulletin
- 1 September 2006
Asymmetric synthesis of methyl ester (4) of (-)-13-oxo-15,16-dinorlabda-8(17),11E-dien-19-oic acid (1), which exhibited the most potent activity for the prevention of incipient carcinogenesis among… Expand
Hydroxamic Acid-Piperidine Conjugate is an Activated Catalyst for Lysine Acetylation under Physiological Conditions.
- S. Mizumoto, Siqi Xi, Yusuke Fujiwara, Shigehiro A Kawashima, K. Yamatsugu, M. Kanai
- Chemistry, Medicine
- Chemistry, an Asian journal
- 3 February 2020
Lysine acylation of proteins is an essential chemical reaction for posttranslational modification and as a means of protein modification in various applications. N,N -Dimethyl-4-aminopyridine (DMAP)… Expand
Nicotinamide derivative or salt thereof as syk-inhibitors
- Hideyasu Fujiwara, K. Sato, +9 authors M. Yamamoto
- Chemistry
- 30 June 2011
Provided are compounds having excellent Syk-inhibitory activity and pharmaceutical compositions. Specifically provided are: nicotinamide derivatives represented by general formula (I) or salts… Expand