Toshiyuki Takahashi

发表

Synthesis, structure-activity relationships, and biological profiles of a dihydrobenzoxathiin class of histamine H(3) receptor inverse agonists.

R. Yoshimoto, Y. Mitobe, Sayaka Ito, 2009, Bioorganic & medicinal chemistry letters.

Design and synthesis of the potent, orally available, brain-penetrable arylpyrazole class of neuropeptide Y5 receptor antagonists.

M. Hirose, N. Fujino, A. Kanatani, 2003, Journal of medicinal chemistry.

Comparison of independent and combined chronic anti-obese effects of NPY Y2 receptor agonist, PYY(3-36), and NPY Y5 receptor antagonist in diet-induced obese mice

H. Iwaasa, A. Kanatani, Y. Mitobe, 2009, Peptides.

Character impact odorants of wild edible plant--Cacalia hastata L. var. orientalis--used in Japanese traditional food.

M. Miyazawa, Toshiyuki Takahashi, Yumi Kawauchi, 2010, Journal of oleo science.

Potent α‐Glucosidase Inhibitors from Safflower (Carthamus tinctorius L.) Seed

M. Miyazawa, Toshiyuki Takahashi, 2012, Phytotherapy research : PTR.

Synergistic interaction between neuropeptide Y1 and Y5 receptor pathways in regulation of energy homeostasis.

H. Iwaasa, H. Matsushita, A. Kanatani, 2009, European journal of pharmacology.

Characteristic odor components of essential oil from Caesalpinia decapetala

M. Miyazawa, Toshiyuki Takahashi, Hiroshi Nakahashi, 2012 .

N-Caffeoyl serotonin as selective COX-2 inhibitor.

M. Miyazawa, Toshiyuki Takahashi, 2012, Bioorganic & medicinal chemistry letters.

Carnosic acid and carnosol inhibit adipocyte differentiation in mouse 3T3-L1 cells through induction of phase2 enzymes and activation of glutathione metabolism.

Y. Takikawa, T. Satoh, Toshiyuki Takahashi, 2009, Biochemical and biophysical research communications.

Discovery of trans-N-[1-(2-fluorophenyl)-3-pyrazolyl]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide, a potent and orally active neuropeptide Y Y5 receptor antagonist.

H. Iwaasa, M. Ando, M. Ishikawa, 2009, Bioorganic & medicinal chemistry.

Aroma evaluation of gamazumi (Viburnum dilatatum) by aroma extract dilution analysis and odour activity value.

M. Miyazawa, T. Kikuchi, Toshiyuki Takahashi, 2012, Phytochemical analysis : PCA.

Characteristic Odor Components of Essential Oil from Dried Fruiting Bodies of Golden Oyster Mushroom (Pleurotus citrinopileatus)

M. Miyazawa, Toshiyuki Takahashi, Yoshiyuki Dejima, 2011 .

Two new aromatic compounds and a new d-arabinitol ester from the mushroom Hericium erinaceum

M. Miyazawa, Toshiyuki Takahashi, I. Horibe, 2012 .

Synthesis and evaluation of a novel indoledione class of long chain fatty acid elongase 6 (ELOVL6) inhibitors.

R. Yoshimoto, T. Nagase, N. Sato, 2009, Journal of medicinal chemistry.

Synthesis and biological evaluation of a novel 3-sulfonyl-8-azabicyclo[3.2.1]octane class of long chain fatty acid elongase 6 (ELOVL6) inhibitors.

R. Yoshimoto, T. Nagase, N. Sato, 2009, Journal of medicinal chemistry.

Biotransformation of serotonin derivatives by the larvae of common cutworm (Spodoptera litura)

M. Miyazawa, Toshiyuki Takahashi, 2013, Natural product research.

Activated glutathione metabolism participates in protective effects of carnosic acid against oxidative stress in neuronal HT22 cells.

T. Satoh, Toshiyuki Takahashi, Kunio Kosaka, 2010, Planta medica.

Metabolism of (+)- and (-)-menthols by CYP2A6 in human liver microsomes.

M. Miyazawa, Shinsuke Marumoto, Toshiyuki Takahashi, 2011, Journal of oleo science.

Synthesis and structure-activity relationships of phenylpropanoid amides of serotonin on tyrosinase inhibition.

M. Miyazawa, Toshiyuki Takahashi, 2011, Bioorganic & medicinal chemistry letters.

Synthesis and structure–activity relationships of serotonin derivatives effect on α-glucosidase inhibition

M. Miyazawa, Toshiyuki Takahashi, 2012, Medicinal Chemistry Research.

Volatile compounds with characteristic odour in moso-bamboo stems (Phyllostachys pubescens Mazel ex Houz. De ehaie).

M. Miyazawa, Toshiyuki Takahashi, Kohji Mizui, 2010, Phytochemical analysis : PCA.

Corrigendum to: Two new aromatic compounds and a new d-arabinitol ester from the mushroom Hericium erinaceum [Tetrahedron 68 (2012) 2007–2010]

M. Miyazawa, Toshiyuki Takahashi, I. Horibe, 2012 .

Discovery and characterization of a novel potent, selective and orally active inhibitor for mammalian ELOVL6.

R. Yoshimoto, T. Ohe, T. Nagase, 2010, European journal of pharmacology.

Synthesis and evaluation of a novel 2-azabicyclo[2.2.2]octane class of long chain fatty acid elongase 6 (ELOVL6) inhibitors.

R. Yoshimoto, T. Nagase, N. Sato, 2009, Bioorganic & medicinal chemistry.

5,5-Dimethyl-3-(5-methyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-1-phenyl-3-(trifluoromethyl)-3,5,6,7-tetrahydro-1H-indole-2,4-dione, a Potent Inhibitor for Mammalian Elongase of Long-Chain Fatty Acids Family 6: Examination of Its Potential Utility as a Pharmacological Tool

R. Yoshimoto, T. Ohe, T. Nagase, 2009, Journal of Pharmacology and Experimental Therapeutics.

Aryl urea derivatives of spiropiperidines as NPY Y5 receptor antagonists.

H. Iwaasa, T. Ohe, A. Kanatani, 2009, Bioorganic & medicinal chemistry letters.

Identification of novel and orally active spiroindoline NPY Y5 receptor antagonists.

D. Macneil, H. Iwaasa, A. Kanatani, 2009, Bioorganic & Medicinal Chemistry Letters.

Novel orally active NPY Y5 receptor antagonists: Synthesis and structure-activity relationship of spiroindoline class compounds.

H. Iwaasa, A. Kanatani, T. Fukami, 2009, Bioorganic & medicinal chemistry.

Novel potent neuropeptide Y Y5 receptor antagonists: synthesis and structure-activity relationships of phenylpiperazine derivatives.

H. Iwaasa, M. Hirose, A. Kanatani, 2006, Bioorganic & medicinal chemistry.

Aryl urea derivatives of spiropiperidines as NPY Y5 receptor antagonists.

H. Iwaasa, T. Ohe, A. Kanatani, 2009, Bioorganic & medicinal chemistry letters.