T. Hata

发表

Crystal Structure of the Extracellular Domain of Mouse RANK Ligand at 2.2-Å Resolution*

Tadashi Hata, Kenji Wakabayashi, S. Ito, 2002, The Journal of Biological Chemistry.

Crystallization and preliminary X-ray crystallographic studies on a Fab fragment of the mouse anti-human Fas monoclonal antibody HFE7A.

T. Takayama, S. Ito, T. Hata, 2001, Acta crystallographica. Section D, Biological crystallography.

Studies on Intermolecular Complex Formation. IV. Crystal Structure of Cytosine-Resorcylic acid 2:1 Complex monohydrate

Sadao. Sato, T. Hata, C. Tamura, 1973 .

6H-anthra[1,9-bc]thiophene derivatives from a bryozoan,Dakaira subovoidea

T. Hata, A. Sato, T. Shindo, 1993, Experientia.

Phomactin A; a novel PAF antagonist from a marine fungus Phoma sp

T. Hata, H. Hanzawa, M. Sugano, 1991 .

The 2.0 Å Crystal Structure of Cyanide Metmyoglobin Reconstituted with 5,10,15,20-Tetrapropylhemin

Y. Hata, Y. Katsube, Takao Sato, 1991 .

Conformational analysis of the 16-membered epoxyenone and complete stereoselection in the reduction of its C9 carbonyl group, the key reaction in the synthesis of maridonolides

N. Nakajima, T. Hata, O. Yonemitsu, 1992 .

Two distinct conformational isomers of the 16-membered epoxyenone, the key synthetic intermediate of maridonolides. Conformational analysis and completely stereoselective reduction of the C9 carbonyl group1)

N. Nakajima, T. Hata, O. Yonemitsu, 1991 .

Reaction of 19-Hydroxysteroids with Diethylaminosulfur Trifluoride.

T. Hata, M. Morisaki, S. Ino, 1991 .

Phomactin E, F, and G: new phomactin-group PAF antagonists from a marine fungus Phoma sp.

T. Hata, M. Sugano, A. Sato, 1995, The Journal of antibiotics.

Physicochemical and crystal structure analyses of the antidiabetic agent troglitazone.

H. Fukuhara, H. Uekusa, Y. Ohashi, 2003, Chemical & pharmaceutical bulletin.

Thiomarinols B and C, new antimicrobial antibiotics produced by a marine bacterium.

K. Fujimoto, T. Hata, S. Takahashi, 1995, The Journal of antibiotics.

Nonsteroidal antiinflammatory drugs. VI: The crystal and molecular structure of (±)-(2S*)-2-[4-((1S*)-2-oxocyclopentylmethyl)phenyl]propionic acid and force-field calculations

Y. Ohashi, T. Hata, Y. Sasada, 1987 .

Nonsteroidal Antiinflammatory Drugs. V. The Crystal and Molecular Structure of (±)-(2S*)-2-[4-((1S*,2R*)-2-hydroxycydopentylmethyl)phenyl]propionic Acid

Sadao. Sato, T. Hata, C. Tamura, 1986 .

The Crystal and Molecular Strucure of Arabinofuranosyladenine Hydrochloride

Sadao. Sato, T. Hata, M. Kaneko, 1974 .

Use of a conformational radical clock for evaluating alkyllithium-mediated cyclization reactions.

T. Hata, S. Rychnovsky, A. Buckmelter, 2001, Organic letters.

Efficient syntheses of a new penem antibiotic, sodium (5R,6S)-2-(2-fluoroethylthio)-6-[(1R)-1-hydroxyethyl]penem-3-carboxylate

I. Kawamoto, T. Hata, R. Endo, 1987 .

Stereoselective Intramolecular Diels-Alder Reactions of α,β-Unsaturated Amides Using Internal Coordination of Metal Salts

T. Hata, N. Iwasawa, T. Mukaiyama, 1983 .

A new antibiotic, mimosamycin

Sadao. Sato, T. Hata, C. Tamura, 1978 .

Phomactins, Novel PAF Antagonists from Marine Fungus Phoma sp.

T. Hata, H. Haruyama, M. Sugano, 1994 .

Angiotensin-converting enzyme inhibitors: perhydro-1,4-thiazepin-5-one derivatives.

S. Miyamoto, T. Hata, H. Koike, 1987, Journal of medicinal chemistry.

Rh(I)-catalyzed formation of two conformers due to cis-1,2-cyclohexanediol

T. Hata, K. Sakai, C. Tamura, 1989 .

Facile Total Synthesis of Carbonolides by Witting-Hoener Macro-Cyclization and Stereoselective Epoxidation

N. Nakajima, K. Uoto, T. Hata, 1991 .

A new synthetic route for the γ-lactone precursors of hydroxyethylene dipeptide isosteres

T. Hata, Y. Yabe, M. Sakurai, 1993 .

Synthesis of the lactone precursor to hydroxyethylene dipeptide isostere from 3,4,6-tri-O-acetyl-D-glucal

T. Hata, M. Shiozaki, Y. Furukawa, 1989 .

Synthesis of renin inhibitors possessing hydroxyethylene isostere residue from 3,4,6-tri-O-acetyl-D-qlucal via lactone precursor

T. Hata, Yoshiyuki Kobayashi, M. Shiozaki, 1991 .

Studies on Intermolecular Complex Formation. II. Crystal Structure of Cytosine-N-Benzoylglycine Complx Monohydrate

Sadao. Sato, T. Hata, C. Tamura, 1972 .

Studies on Intermolecular Complex Formation. III. Crystal Structure of Thymine-N,N-Diethylmelamine Complex Monohydrate

Sadao. Sato, T. Hata, C. Tamura, 1973 .

Studies on intermolecular complex formation. VII. Crystal structure of adenosine–5‐bromouracil

Sadao. Sato, T. Hata, C. Tamura, 1978 .

CRYSTAL STRUCTURE OF CYTIDINE-SALICYLIC ACID COMPLEX

Sadao. Sato, T. Hata, C. Tamura, 1973 .

Structure of plaunolide, a new furanoid diterpene from Croton sublyratus, C20H20O5

T. Hata, H. Haruyama, C. Tamura, 1983 .

Plaunol A and B, new anti-ulcer diterpenelactones from

T. Hata, H. Kuwano, Shuji Takahashi, 1979 .

Molecular structure of 2-troponylcyanomethylenetriphenylphosphonium betaine

I. Kawamoto, T. Hata, C. Tamura, 1971 .

Immunological studies on sporamycin-treated animals.

T. Hata, K. Komiyama, I. Umezawa, 1979, The Journal of antibiotics.

1:1 Cytidine-N-carbobenzoxyglutamic acid dihydrate

Sadao. Sato, T. Hata, C. Tamura, 1975 .

Chatancin, a PAF antagonist from a soft coral, Sarcophyton sp

T. Hata, M. Sugano, A. Sato, 1990 .

Milbemycin derivatives: epoxidation of milbemycins.

T. Hata, A. Saito, S. Naito, 1994, The Journal of antibiotics.

Effects of (+)-, (-)- and (+/-)-indenestrols A and B on microtubule polymerization.

T. Hata, H. Hanzawa, Y. Sakakibara, 1992, Chemical & pharmaceutical bulletin.

In situ observation of the four-step dehydration process of the 1 beta-methylcarbapenem antibiotic CS-834 crystal by X-rays.

H. Fukuhara, Y. Ohashi, T. Hata, 2003, Chemical & pharmaceutical bulletin.

Physicochemical analyses of phase transition and dehydration processes of a new oral 1beta-methylcarbapenem antibiotic agent, CS-834.

H. Fukuhara, I. Kawamoto, H. Uekusa, 2002, Chemical & pharmaceutical bulletin.

A study of immunosuppressive effect of antitumor agents.

T. Hata, K. Komiyama, I. Umezawa, 1972, The Kitasato archives of experimental medicine.

Iyomycin, a new antitumor antibiotic from Streptomyces. IV. Experimental treatment of malignant tumors with iyomycins.

T. Hata, M. Hoshino, I. Umezawa, 1967, The Journal of antibiotics.

IYOMYCIN, A NEW ANTITUMOR ANTIBIOTIC FROM STREPTOMYCES. III. ISOLATION AND PROPERTIES OF IYOMYCIN B.

T. Hata, Y. Sano, N. Kanda, 1964, The Journal of antibiotics.

Humanization of the mouse anti-Fas antibody HFE7A and crystal structure of the humanized HFE7A Fab fragment.

S. Yonehara, T. Takayama, S. Ito, 2002, Biological & pharmaceutical bulletin.

Mimosamycin, a novel antibiotic produced by streptomyces lavendulae no. 314: structure and synthesis

T. Hata, T. Arai, A. Kubo, 1977 .

The synthesis of hexahydrooxoepithiopyridinedicarboximides by the reaction of thioamides with N-substituted maleimides

T. Hata, M. Senō, S. Tamura, 1998 .

X-ray study of baker's yeast lipoamide dehydrogenase at 4.5 A resolution by molecular replacement method.

T. Hata, A. Takénaka, S. Sato, 1988, Journal of biochemistry.

Thiomarinols B and C, New Antimicrobial Antibiotics Produced by a Marine Bacterium

K. Fujimoto, T. Hata, Shuji Takahashi, 1996 .

Phomactin A: A Novel PAF Antagonist from a Marine Fungus Phoma sp.

T. Hata, H. Hanzawa, M. Sugano, 1991 .

Crystal structure of RANK ligand involved in bone metabolism.

S. Ito, T. Hata, 2004, Vitamins and hormones.

Studies on mitomycin C, especially method of administration.

T. Hata, H. Takita, C. Hossenlopp, 1961, Cancer chemotherapy reports.

Aldose reductase inhibitors from a marine sponge, Dictyodendrilla sp.

H. Horikoshi, T. Hata, H. Hanzawa, 1993 .

Aldose Reductase Inhibitors (I) and (II) from a Marine Sponge, Dictyodendrilla sp.

H. Horikoshi, T. Hata, H. Hanzawa, 1994 .

Crystal Structure of a 1β-Methylcarbapenem Antibiotic, Pivaloyloxymethyl (1R,5S,6S)-6-[(R)-1-hydroxyethyl]-1-methyl-2-[[(R)-5-oxopyrrolidin-3-yl]thio]-1-carbapen-2-em-3-carboxylate, CS-834 Dihydrate

H. Fukuhara, I. Kawamoto, S. Ito, 2001, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

Crystal structure of the antigen-binding fragment of apoptosis-inducing mouse anti-human Fas monoclonal antibody HFE7A.

T. Takayama, S. Ito, T. Hata, 2002, Journal of biochemistry.

Crystallization and preliminary X-ray diffraction analysis of cytochrome P450sca-2 from Streptomyces carbophilus involved in production of pravastatin sodium, a tissue-selective inhibitor of HMG-CoA reductase.

S. Ito, T. Hata, N. Serizawa, 1999, Acta crystallographica. Section D, Biological crystallography.

Structural study of triazole antifungals. II : Crystal and molecular structures of the two diastereoisomers (4R*,5R*)- and (4S*,5R*)-5-(2,4-difluorophenyl)-4-methyl-5[(1H-1,2,4-triazol-1-yl)methyl]-3-[4-(trifluoromethyl)benzoyl]oxazolidine

T. Hata, T. Konosu, Y. Furukawa, 1991 .

RhI-catalysed formation of two conformational diastereoisomers due to a cis-cyclohexane-1,2-diol moiety. X-Ray molecular structure of two stereoisomers of 4′-isopropenyl-7,9-dioxabicyclo[4.3.0]nonane-8-spirocyclohexan-3′-yl p-bromobenzoate

T. Hata, Xiaomei Wu, K. Sakai, 1991 .

RhI-Catalyzed Formation of Two Conformational Diastereoisomers Due to a cis-Cyclohexane-1,2-diol Moiety. X-Ray Molecular Structure of Two Stereoisomers of 4′-Isopropenyl-7,9-dioxabicyclo(4.3.0)nonane-8- spirocyclohexan-3′-yl p-Bromobenzoate.

T. Hata, N. Marubayashi, K. Funakoshi, 1992 .

Bromination of Biphenylene Derivatives Having an Electron-releasing Substituent. A Preferential Formation of Benzocyclooctene Derivatives

Sadao. Sato, T. Hata, Yuko Saito, 1983 .