T. Fukami

发表

Discovery of 6-benzyloxyquinolines as c-Met selective kinase inhibitors.

H. Sakamoto, T. Chiba, Hiroki Nishii, 2010, Bioorganic & medicinal chemistry letters.

Purification, crystallization, and preliminary X-ray crystallographic analysis of thermus thermophilus V(1)-ATPase B subunit.

K. Miki, T. Nogi, T. Fukami, 1999, Journal of structural biology.

Purification, crystallization and preliminary X-ray diffraction studies of UDP-N-acetylglucosamine pyrophosphorylase from Candida albicans.

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Crystallization and preliminary X-ray characterization of chaperonin-60 from Paracoccus denitrificans

Masasuke Yoshida, M. Yohda, K. Miki, 1996 .

Synthesis and structure-activity relationships of novel benzofuran farnesyltransferase inhibitors.

M. Sakaitani, T. Fukami, N. Shimma, 2009, Bioorganic & medicinal chemistry letters.

CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant.

Hiroshi Sakamoto, H. Sakamoto, T. Fukami, 2011, Cancer cell.

Design and synthesis of 2-amino-6-(1H,3H-benzo[de]isochromen-6-yl)-1,3,5-triazines as novel Hsp90 inhibitors.

Shigeo Sato, Sung-jin Kim, K. Kawasaki, 2014, Bioorganic & medicinal chemistry.

Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase I inhibitors.

H. Sakamoto, T. Chiba, T. Fukami, 2012, Bioorganic & medicinal chemistry letters.

Crystal Structures of N-Acetylglucosamine-phosphate Mutase, a Member of the α-d-Phosphohexomutase Superfamily, and Its Substrate and Product Complexes*

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2006, Journal of Biological Chemistry.

The Crystal Structure and Stereospecificity of Levodione Reductase from Corynebacterium aquaticum M-13*

M. Wada, H. Takagi, S. Sogabe, 2003, Journal of Biological Chemistry.

Crystal structure of chaperonin-60 from Paracoccus denitrificans.

H. Taguchi, M. Yohda, M. Yoshida, 2001, Journal of molecular biology.

Crystal structures of Candida albicans N-myristoyltransferase with two distinct inhibitors.

F. Winkler, D. Banner, A. D'arcy, 2002, Chemistry & biology.

Lead generation of heat shock protein 90 inhibitors by a combination of fragment-based approach, virtual screening, and structure-based drug design.

Sung-jin Kim, K. Hasegawa, T. Fukami, 2011, Bioorganic & medicinal chemistry letters.

Design and synthesis of novel macrocyclic 2-amino-6-arylpyrimidine Hsp90 inhibitors.

Atsushi Suda, Hiroshi Koyano, Naomi Ono, 2012, Bioorganic & medicinal chemistry letters.

Utilization of microgravity to improve the crystal quality of biologically important proteins: chaperonin-60, GrpE, B-subunit of V-type ATPase, and MIF

I. Tanaka, A. Nakagawa, K. Miki, 2000 .

Discovery of 6‐Benzyloxyquinolines as c‐Met Selective Kinase Inhibitors.

H. Sakamoto, T. Chiba, Hiroki Nishii, 2010 .

Crystal Structure of Uridine-diphospho-N-acetylglucosamine Pyrophosphorylase from Candida albicans and Catalytic Reaction Mechanism*

K. Miki, Y. Nishitani, T. Yamada-Okabe, 2007, Journal of Biological Chemistry.

Purification, crystallization and preliminary X-ray diffraction studies of N-acetylglucosamine-phosphate mutase from Candida albicans

K. Miki, Y. Nishitani, T. Fukami, 2006, Acta crystallographica. Section F, Structural biology and crystallization communications.

Design and evaluation of azaindole-substituted N-hydroxypyridones as glyoxalase I inhibitors.

H. Sakamoto, T. Chiba, T. Fukami, 2012, Bioorganic & medicinal chemistry letters.

Fluorescence Compounds Contained in Tumor

I. Okura, T. Fukami, T. Nishisaka, 1995 .