Yuuki Koide

发表

Pharmacophore-Based Drug Discovery and Its Application

Naoki Okada, Yuuki Koide, N. Okada, 2015 .

Topics on the Na+/Ca2+ exchanger: pharmacological characterization of Na+/Ca2+ exchanger inhibitors.

J. Kimura, Yasuhide Watanabe, Yuuki Koide, 2006, Journal of pharmacological sciences.

Forum Minireview Topics on the Na + / Ca 2+ Exchanger: Pharmacological Characterization of Na + / Ca 2+ Exchanger Inhibitors

J. Kimura, Yasuhide Watanabe, Yuuki Koide, 2006 .

Stability on Drying of Cyclodextrin Precipitates of Volatile Nonelectrolytes.

I. Sanemasa, Yue Wu, T. Deguchi, 1994 .

Involvement of p38 MAP kinase-mediated cytochrome c release on sphingosine-1-phosphate (S1P)- and N-monomethyl-S1P-induced cell death of PC12 cells.

A. Nishida, Hiroyuki Nakamura, T. Murayama, 2005, Biochemical pharmacology.

Sphingosine 1-Phosphate (S1P) Regulates Vascular Contraction via S1P 3 Receptor: Investigation Based on a New S1P 3 Receptor Antagonist S

N. Mochizuki, N. Takakura, T. Konno, 2010 .

Sphingosine 1-Phosphate (S1P) Regulates Vascular Contraction via S1P 3 Receptor: Investigation Based on a New

N. Mochizuki, N. Takakura, A. Murakami, 2010 .

Sphingosine 1-Phosphate ( S 1 P ) Regulates Vascular Contraction via S 1 P 3 Receptor : Investigation Based on a New S 1 P 3 Receptor Antagonist

N. Mochizuki, N. Takakura, A. Murakami, 2010 .

Effects of synthetic sphingosine-1-phosphate analogs on cytosolic phospholipase A2alpha-independent release of arachidonic acid and cell toxicity in L929 fibrosarcoma cells: the structure-activity relationship.

A. Nishida, Y. Muramatsu, Hiroyuki Nakamura, 2009, Journal of pharmacological sciences.

Development of novel EDG3 antagonists using a 3D database search and their structure-activity relationships.

N. Mochizuki, A. Nishida, A. Endo, 2002, Journal of medicinal chemistry.

Preparation of Cyclodextrin Precipitates with Volatile Hydrocarbons in Aqueous Media, and Determination of Hydrocarbon/Cyclodextrin Molar Ratios in the Precipitates

I. Sanemasa, Yue Wu, T. Deguchi, 1993 .

Isomer Compositions of Trimethyl- or Trichlorobenzenes in α-Cyclodextrin Precipitates Formed in an Aqueous Medium

K. Toda, I. Sanemasa, Yue Wu, 1996 .

Structure-activity relationship of benzo[b]thiophene-2-sulfonamide derivatives as novel human chymase inhibitors.

A. Murakami, Y. Mizuno, Yuuki Koide, 2003, Bioorganic & medicinal chemistry letters.

Sphingosine 1-Phosphate (S1P) Regulates Vascular Contraction via S1P3 Receptor: Investigation Based on a New S1P3 Receptor Antagonist

N. Mochizuki, N. Takakura, A. Murakami, 2010, Molecular Pharmacology.

Identification of a stable chymase inhibitor using a pharmacophore-Based database search.

A. Murakami, Hideki Yamada, T. Hasegawa, 2003, Bioorganic & medicinal chemistry letters.

Newly synthetic ceramide-1-phosphate analogs; their uptake, intracellular localization, and roles as an inhibitor of cytosolic phospholipase A(2)α and inducer of cell toxicity.

A. Nishida, Hiroyuki Nakamura, T. Murayama, 2010, Biochemical pharmacology.

Effects of synthetic sphingosine-1-phosphate analogs on arachidonic acid metabolism and cell death.

A. Nishida, Hiroyuki Nakamura, T. Murayama, 2004, Biochemical pharmacology.

Characterization of two putative mechanosensitive channel proteins of Campylobacter jejuni involved in protection against osmotic downshock.

T. Kakuda, Aya Sakamoto, S. Takai, 2012, Veterinary microbiology.