H. Satō

发表

Trifluoromethyl ketone inhibitors of fatty acid amide hydrolase: a probe of structural and conformational features contributing to inhibition.

D. Boger, B. Cravatt, H. Satō, 1999, Bioorganic & medicinal chemistry letters.

Arachidonic acid amide inhibitors of gap junction cell-cell communication.

D. Boger, N. Gilula, H. Satō, 1999, Bioorganic & medicinal chemistry letters.

Exceptionally potent inhibitors of fatty acid amide hydrolase: the enzyme responsible for degradation of endogenous oleamide and anandamide.

D. Boger, B. Cravatt, M. Hedrick, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Antioxidant action of sugar-pendant C60 fullerenes.

E. Niki, Yoshiro Saito, H. Satō, 2009, Bioorganic & medicinal chemistry letters.

Synthesis and some Physical Properties of trans-4–{β-(trans-4′-n-Alkylcyclohexyl)-1′} -Ethylcyclohexane-1 -Carboxylates

H. Takatsu, H. Satō, K. Takeuchi, 1984 .

Synthesis and some physical properties of 1-cyclohexyl-2-(4''-halobiphenyl-4'-yl) ethanes

H. Takatsu, H. Satō, K. Takeuchi, 1983 .

Roles of mast cells and sensory nerves in cutaneous vascular hyperpermeability and scratching behavior induced by poly-L-arginine in rats.

H. Satō, A. Ishii, A. Karasawa, 2001, European journal of pharmacology.

Electron-Transporting Polymers Having Side-Chain Fluorene Derivatives for Use as N-Type Organic Photoreceptors.

K. Ogino, H. Satō, J. Sim, 1996 .

The chemistry of indoles. CIII. Simple syntheses of serotonin, N-methylserotonin, bufotenine, 5-methoxy-N-methyltryptamine, bufobutanoic acid, N-(indol-3-yl)methyl-5-methoxy-N-methyltryptamine, and lespedamine based on 1-hydroxyindole chemistry.

H. Satō, M. Somei, C. Kaneko, 2001, Chemical & pharmaceutical bulletin.

Studies on uricosuric diuretics. II. Substituted 7,8-dihydrofuro[2,3-g]-1,2-benzisoxazole-7-carboxylic acids and 7,8-dihydrofuro[2,3-g]benzoxazole-7-carboxylic acids.

H. Satō, E. Onuma, H. Koga, 1991, Chemical & pharmaceutical bulletin.

6-Substituted 2,2-bis(fluoromethyl)-benzopyran-4-carboxamide K+ channel openers.

H. Satō, H. Koga, J. Imagawa, 2000, Bioorganic & medicinal chemistry.

Synthesis and vasorelaxant activity of 2-fluoromethylbenzopyran potassium channel openers.

H. Satō, H. Koga, J. Imagawa, 1998, Bioorganic & medicinal chemistry.

Synthesis and reduction of (S)-(-)-nicotine-N’-oxide and N,N’-dioxides by rat liver S-9 fraction

H. Satō, K. Uwai, M. Takeshita, 2003 .

Practical synthesis of a 1beta-methylcarbapenem, J-111,225, using 4-mercapto-2-[4-(N-methylaminomethyl)phenyl]pyrrolidine as a precursor.

S. Sakuraba, H. Satō, H. Morishima, 2001, Chemical & pharmaceutical bulletin.

A convenient synthesis of α,ω‐diamino substituted oligo(oxyethylene)s

W. Kern, H. Satō, V. Böhmer, 1979 .

Novel dithiocarbamate carbapenems with anti-MRSA activity.

H. Satō, N. Ohtake, M. Moriya, 1997, Bioorganic & medicinal chemistry.

Discovery of novel trans-3,5-disubstituted pyrrolidinylthio-1beta-methylcarbapenems.

Y. Tsuchiya, S. Sakuraba, H. Satō, 2000, Bioorganic & medicinal chemistry.

A novel 1beta-methylcarbapenem, J-111,225: effects of the C-3 and C-5 stereochemistry of the pyrrolidinylthio side chain on antibacterial activities.

S. Sakuraba, H. Satō, H. Morishima, 2000, The Journal of antibiotics.

Solvent dependency of the steric course of dienolate alkylation

K. Nakanishi, H. Satō, Y. Nakadaira, 1972 .

Structural aspects of photosensitized β,γ-enone isomerizations

K. Nakanishi, H. Satō, Y. Nakadaira, 1973 .

Quantitative structure-activity relationships of antibacterial agents, 7-heterocyclic amine substituted 1-cyclopropyl-6,8-difluoro-4-oxoquinoline-3-carboxylic acids.

H. Satō, T. Okada, K. Ezumi, 1993, Chemical & pharmaceutical bulletin.

Synthesis of Polymers Having a Hole Transporting Ability by Condensation Polymerization of N,N‘-Diphenyl-N,N‘-bis(4-methylphenyl)-(1,1‘-biphenyl)-4,4‘-diamine and Aldehydes

K. Ogino, H. Satō, Y. Ito, 1999 .

SYNTHESIS OF FULLEROTETRAHYDROQUINOLINES BY CYCLOADDITION REACTION OF C60 WITH AZA-ORTHO-XYLYLENES

S. Eguchi, H. Satō, M. Ohno, 1999 .

Synthesis of a dibenz[b,e]oxepin-bovine serum albumin conjugate for radioimmunoassay of KW-4679 ((Z)-11-[3-(dimethylamino)propylidene]-6,11- dihydrodibenz[b,e]oxepin-2-acetic acid hydrochloride).

T. Kuwabara, S. Kobayashi, H. Satō, 1992, Chemical & pharmaceutical bulletin.

Synthesis and antiallergic activity of 11-(aminoalkylidene)-6,11-dihydrodibenz[b,e]oxepin derivatives.

H. Ishii, H. Satō, N. Hirayama, 1992, Journal of medicinal chemistry.

Synthesis and Some Properties of Nematic Compounds Containing Three Ring Systems

H. Takatsu, H. Satō, K. Takeuchi, 1984 .

Synthesis and some properties of 3,4-difluorophenyl trans-4'-substituted cyclohexane-1'-carboxylates

H. Takatsu, H. Satō, K. Takeuchi, 1984 .

Incorporation of 1,1'-dibenzyl-4,4'-bipyridinium cation into Nafion films and charge transport in loaded film electrodes

Takahiro Yamaguchi, H. Satō, T. Yamaguchi, 2001 .

Synthesis and structure-activity relationships of 7-(3'-amino-4'-methoxypyrrolidin-1'-yl)-1-cyclopropyl-6,8-difluoro-1,4- dihydro-4-oxoquinoline-3-carboxylic acids.

H. Satō, H. Nakai, T. Okada, 1993, Chemical & pharmaceutical bulletin.

Synthesis and anti-HIV activity of 9-[c-4,t-5-bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine.

T. Tsuruo, H. Satō, K. Yusa, 1992, Journal of medicinal chemistry.

Resolution of 9-(c-4,t-5-bishydroxymethylcyclopent-2-en-r-1-yl)-9H-adenine and selective inhibition of human immunodeficiency virus by the (-) enantiomer.

T. Tsuruo, T. Shiraishi, H. Satō, 1992, Biochemical and biophysical research communications.

Configurational and conformational studies of sugars by the aromatic chirality method

K. Nakanishi, N. Harada, H. Satō, 1970 .

Dibenzoxepin derivatives: thromboxane A2 synthase inhibition and thromboxane A2 receptor antagonism combined in one molecule.

I. Miki, K. Kubo, H. Satō, 1993, Journal of medicinal chemistry.

Practical asymmetric synthesis of a selective endothelin A receptor (ETA) antagonist.

H. Satō, T. Nemoto, R. Volante, 2001, Organic Letters.

Non-prostanoid thromboxane A2 receptor antagonists with a dibenzoxepin ring system. 2.

I. Miki, K. Kubo, H. Satō, 1992, Journal of medicinal chemistry.