T. Noshita

发表

Molecular docking and structural analysis of cofactor-protein interaction between NAD+ and 11β-hydroxysteroid dehydrogenase type 2

K. Ryoyama, T. Akitaya, H. Yamaguchi, 2012, Journal of Molecular Modeling.

Isolation of Ursolic Acid from Apple Peels and Its Specific Efficacy as a Potent Antitumor Agent

M. Hayashi, K. Ryoyama, K. Komiyama, 2008 .

Mouse 11β-Hydroxysteroid Dehydrogenase Type 2 for Human Application: Homology Modeling, Structural Analysis and Ligand-Receptor Interaction

K. Ryoyama, T. Akitaya, H. Yamaguchi, 2011, Cancer informatics.

Intracellular accumulation of structurally varied isothiocyanates correlates with inhibition of nitric oxide production in proinflammatory stimuli-activated tumorigenic macrophage-like cells.

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2014, Bioorganic & medicinal chemistry.

Detection of 6-(methylsulfinyl)hexyl isothiocyanate (6-MITC) and its conjugate with N-acetyl-L-cysteine (NAC) by high performance liquid chromatograpy-atmospheric pressure chemical ionization mass spectrometry (HPLC-MS/APCI).

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2008, Chemical & pharmaceutical bulletin.

Anti-influenza virus principles from Muehlenbeckia hastulata

Yoshitaka Shimotai, M. Yamaki, S. Funayama, 2010, Journal of Natural Medicines.

Structure–activity relationships of flavanones, flavanone glycosides, and flavones in anti-degranulation activity in rat basophilic leukemia RBL-2H3 cells

A. Tai, T. Noshita, H. Ouchi, 2018, Journal of Natural Medicines.

Structure-activity relationship of flavanone. Anti-degranulation activity of 7-O-substituted hesperetin

A. Tai, T. Noshita, K. Ikeda, 2017, Natural product research.

Synthesis and degranulation-inhibiting activities of the proposed apteniols B, C, and G

A. Saito, A. Tai, T. Noshita, 2015, Bioscience, biotechnology, and biochemistry.

Syntheses and biological activities of the proposed structure of apteniol A and its derivatives

A. Saito, A. Tai, T. Noshita, 2014, Bioscience, biotechnology, and biochemistry.

Novel effects of glycyrrhetinic acid on the central nervous system tumorigenic progenitor cells: induction of actin disruption and tumor cell-selective toxicity.

K. Ryoyama, H. Yamaguchi, Tao Yu, 2010, European journal of medicinal chemistry.

Phenolic ferrier reaction and its application to the natural product synthesis

T. Oritani, T. Noshita, Takekatsu Sugiyama, 1994 .

The proposed structures of phenolic compounds isolated from Piper betle L. differ from those of the compounds obtained by total synthesis

T. Noshita, H. Ouchi, T. Sato, 2020, Natural product research.

Total Synthesis of Natural (+)-Phomopsolide B

T. Noshita, T. Sugiyama, K. Yamashita, 1991 .

New Quinoline Alkaloids from the Leaves and Stems of Orixa japonica, Orijanone, Isopteleflorine and 3'-O-Methylorixine

S. Funayama, T. Noshita, K. Murata, 2001, Bioscience, biotechnology, and biochemistry.

Isolation of ethyl caffeate from the petals of Prunus yedoensis

S. Funayama, T. Noshita, Ai Sakaguchi, 2006, Journal of Natural Medicines.

Adxanthromycins A and B, new inhibitors of ICAM-1/LFA-1 mediated cell adhesion molecule from Streptomyces sp. NA-148. II. Physico-chemical properties and structure elucidation.

H. Koshino, A. Nakagawa, S. Takahashi, 2000, The Journal of antibiotics.

Characterization of (-)-matairesinol as a potent inhibitor of casein kinase I in vitro.

S. Funayama, K. Ohtsuki, T. Noshita, 2003, Biological & pharmaceutical bulletin.

Synthesis and biological activity of (±)-7,3',4'-trihydroxyhomoisoflavan and its analogs.

A. Tai, T. Noshita, H. Ouchi, 2020, Bioorganic & medicinal chemistry letters.

Total synthesis of natural (+)-phomopsolide B, an antifeedant against elm bark beetle

T. Oritani, T. Noshita, T. Sugiyama, 1994 .

Neurite Outgrowth-Promoting Compounds from the Petals of Paeonia lactiflora in PC12 Cells

Hideyuki Ito, A. Tai, T. Noshita, 2022, Molecules.

Preparation of the Extracellular Domain of Recombinant Human Toll-like Receptor 6

M. Tanokura, T. Miyakawa, T. Noshita, 2017, The Protein Journal.

Prediction of the possible inhibitory effect of 6- (methylsulfinyl)hexyl isothiocyanate (6MITC) and its analogs on P-glycoprotein (P-gp) by in silico analysis of their interaction energies

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2013 .

New Cytotoxic Phenolic Derivatives from Matured Fruits of Magnolia denudata

K. Ryoyama, H. Kiyota, T. Murayama, 2009, Bioscience, biotechnology, and biochemistry.

Structural insight into the ligand-receptor interaction between glycyrrhetinic acid (GA) and the high-mobility group protein B1 (HMGB1)-DNA complex

Hideaki Yamaguchi, Yumi Kidachi, Katsuyoshi Kamiie, 2012, Bioinformation.

Machilin G and Four Neolignans from Young Fruits of Magnolia denudata Show Various Degrees of Inhibitory Activity on Nitric Oxide (NO) Production

K. Ryoyama, S. Funayama, Y. Kidachi, 2008, Bioscience, biotechnology, and biochemistry.

Utilization of 6-(methylsulfinyl)hexyl isothiocyanate for sensitization of tumor cells to antitumor agents in combination therapies.

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2013, Biochemical pharmacology.

Structural insight into the ligand-receptor interaction between 6-(methylsulfinyl)hexyl isothiocyanate and multidrug resistance-associated protein 1 nucleotide-binding domain 1

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2014 .

Excess carotenoids disturb prospective cell-to-cell recognition system in mating responses ofPhycomyces blakesleeanus

Shunya Takahashi, T. Ootaki, T. Noshita, 1996 .

Homology modeling and structural analysis of 11β-hydroxysteroid dehydrogenase type 2.

K. Ryoyama, T. Akitaya, H. Yamaguchi, 2011, European journal of medicinal chemistry.

Selective cytotoxicity of glycyrrhetinic acid against tumorigenic r/m HM-SFME-1 cells: potential involvement of H-Ras downregulation.

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2010, Toxicology letters.

Selective toxicity of glycyrrhetinic acid against tumorigenic r/m HM-SFME-1 cells is potentially attributed to downregulation of glutathione.

K. Ryoyama, T. Akitaya, H. Yamaguchi, 2011, Biochimie.

Ligand-receptor Interaction between Triterpenoids and the 11β-Hydroxysteroid dehydrogenase type 2 (11βHSD2) Enzyme Predicts Their Toxic Effects against Tumorigenic r/m HM-SFME-1 Cells*

K. Ryoyama, Kenji Yoshida, T. Akitaya, 2011, The Journal of Biological Chemistry.

Synthetic and in vitro studies to indicate that the structure of the PTP1B inhibitor isolated from Acanthopanax senticosus requires reinvestigation

A. Tai, T. Noshita, Y. Nishino, 2018, Phytochemistry Letters.

The structure proposed for apteniol D is different from that of the compound obtained by total synthesis

A. Saito, T. Noshita, H. Ouchi, 2017, Natural product research.

Anti-nitric oxide production activity of isothiocyanates correlates with their polar surface area rather than their lipophilicity.

K. Ryoyama, H. Kiyota, H. Yamaguchi, 2009, European journal of medicinal chemistry.

The Augmenting Activity of 6-(Methylsulfinyl)hexyl Isothiocyanate on Cellular Glutathione Levels Is Less Sensitive to Thiol Compounds Than Its Cytotoxic Activity

K. Ryoyama, H. Yamaguchi, Y. Kidachi, 2009, Bioscience, biotechnology and biochemistry.

Structural basis for the interaction of 6-(methylsulfinyl) hexyl isothiocyanate with inducible nitric oxide synthase