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Pharmaceutical Research Center Meiji Seika Kaisha Ltd. | 論文
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics II. Preparation of Pharmacokinetically Improved Analogues via Biotransformation
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics I. Synthesis of 4-O-Alkyl-L-cladinose Analogues via Glycosylation
- 抵抗性誘導物質の作用機構 (特集号 植物感染生理の新展開)
- Application of Polymer Supported Base in Solid Phase Synthesis: Convenient Synthesis of N-Aryl-N'-benzyl Piperazine Derivatives
- Purification and Properties of a Prokaryote Type Glutamine Synthetase from the Bialaphos Producer Streptomyces hygroscopicus SF1293
- Role of the α subunit of heterotrimeric G-protein in probenazole-inducing defense signaling in rice
- Synthesis of the Selective 5-Hydroxytryptamine 4 (5-HT_4) Receptor Agonist (+)-(S)-2-Chloro-5-methoxy-4-[5-(2-piperidylmethyl)-1,2,4-oxadiazol-3-yl]aniline
- Model Study for Preparation of asymmetric N, N'-Disubstituted piperazine Library:Efficient Synthesis of Aryl Piperazine and Benzyl Piperazine Derivatives on the Solid Support
- Cladinose Analogues of Sixteen-membered Macrolide Antibiotics III. Efficient Synthesis of 4-0-Alkyl-L-cladinose Analogues: Improved Antibacterial Activities Compatible with Pharmacokinetics
- Novel 5-Hydroxytryptamine 4 (5-HT_4) Receptor Agonists. Synthesis and Gastroprokinetic Activity of 4-Amino-N-[2-(1-aminocycloalkan-1-yl)ethyl]-5-chloro-2-methoxybenzamides
- 経口セフェム剤セフジトレンピボキシルの開発
- Superoxide Anion Generation in Rice Blade Protoplasts with the Blast Fungus Proteoglucomannan Elicitor as Determined by CLA-phenyl Luminescence and Its Suppression by Treating the Elicitor withα-D-Mannosidase
- Comparison of Noradrenergic and Serotonergic Antidepressants in Reducing Immobility Time in the Tail Suspension Test
- Enhancement of Hepatocyte Growth Factor-Induced Cell Scattering in N-Acetylglucosaminyltransferase III-transfected HepG2 Cells(Biochemistry/Molecular Biology)
- Novel 5-Hydroxytryptamine (5-HT_3) Receptor Antagonists. Synthesis and Structure-Activity Relationships of 9-Methyl-2,3,4,9-tetrahydrothiopyrano[2,3-b]indol-4-one Derivatives
- Novel 5-Hydroxytryptamine (5-HT_3) Receptor Antagonists. IV. Synthesis and Pharmacological Evaluation of the Oxidation Products of (-)-(R)-5-[(1-Methyl-1H-indol-3-yl)carbonyl]-4,5,6,7-tetrahydro-1H-benzimidazole Hydrochloride (YM060 : Ramosetron)
- Novel 5-Hydroxytryptamine (5-HT_3) Receptor Antagonists. III. Pharmacological Evaluations and Molecular Modeling Studies of Optically Active 4,5,6,7-Tetrahydro-1H-benzimidazole Derivatives
- Novel 5-Hydroxytryptamine (5-HT_3) Receptor Antagonists. II. Synthesis and Structure-Activity Relationships of 4,5,6,7-Tetrahydro-1H-benzimidazole Derivatives
- Novel 5-Hydroxytryptamine (5-HT_3) Receptor Antagonists. I. Synthesis and Structure-Activity Relationships of Conformationally Restricted Fused Imidazole Derivatives
- Antisecretory and Antiulcer Effects of YM020, a New H^+, K^+-ATPase Inhibitor, in Rats and Dogs
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