Research Topics
| J KoyamaSummaryAffiliation: Kobe Pharmaceutical University Country: Japan Publications
| Collaborators
|
Detail Information
Publications
Cyclopentene dialdehydes from Tabebuia impetiginosaJ Koyama
Kobe Pharmaceutical University, Japan
Phytochemistry 53:869-72. 2000..The structures were established by analysis of spectroscopic data. These compounds showed anti-inflammatory activity...
Simultaneous determination of histamine and prostaglandin D2 using an LC-ESI-MS/MS method with positive/negative ion-switching ionization modes: application to the study of anti-allergic flavonoids on the degranulation of KU812 cellsJunko Koyama
Kobe Pharmaceutical University, Higashinada, Kobe, Japan
Anal Bioanal Chem 401:1385-92. 2011..2% and 7.8% for PGD(2). This method was used to evaluate the anti-allergic effects of 26 flavonoids and sodium cromoglicate which are first-line anti-allergic drugs. Of these compounds, baicalein and morin were the most potent inhibitors...
Simultaneous determination of anthraquinones, their 8-beta-D-glucosides, and sennosides of Rhei Rhizoma by capillary electrophoresisJunko Koyama
Kobe Pharmaceutical University, Kobe 658 8558, Japan
Chem Pharm Bull (Tokyo) 53:573-5. 2005..The running electrolyte used in this method was 0.005 M alpha-cyclodextrin in 0.03 M borate buffer (pH 10.0) containing 20% acetonitrile, with an applied voltage of 20 kV...
Correlation between reduction potentials and inhibitory effects on Epstein-Barr virus activation of poly-substituted anthraquinonesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Cancer Lett 225:193-8. 2005..It has been further shown that the correlation can be enhanced by introducing log P as an additional parameter...
Correlation between reduction potentials and inhibitory effects on Epstein-Barr virus activation by emodin derivativesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Cancer Lett 241:263-7. 2006..The electronic properties, i.e. LUMO energy and atomic charges of carbon at the 9-position (C(9)) and oxygen at the 11-position (O(11)), may also be useful for estimating the inhibitory effect on EBV-EA activation...
Antiallergic activity of aqueous extracts and constituents of Taxus yunnanensisJunko Koyama
Kobe Pharmaceutical University, Japan
Biol Pharm Bull 29:2310-2. 2006..A new neolignan, 2-[2-hydroxy-5-(3-hydroxypropyl)-3-methoxyphenyl]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol, was isolated from the wood of Taxus yunnanensis...
Simultaneous determination of anthraquinones in rhubarb by high-performance liquid chromatography and capillary electrophoresisJunko Koyama
Kobe Pharmaceutical University, Higashinada ku, Kobe 658 8558, Japan
J Chromatogr A 1145:183-9. 2007....
Anti-infective quinone derivatives of recent patentsJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada ku, Kobe 658 8558, Japan
Recent Pat Antiinfect Drug Discov 1:113-25. 2006..This review will focus on the preparation, therapeutic application, and administration of several benzoquinones, naphthoquinones, and anthraquinones having anti-infective, e.g. antiviral and antibacterial activities, in recent patents...
Correlation between oxidation potentials and inhibitory effects on Epstein-Barr virus activation of flavonoidsJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Cancer Lett 263:61-6. 2008..Furthermore, multiple regression analysis revealed that the solvent-accessible surface area (SASA) was a useful parameter for estimating the inhibitory effects of flavonoids on EBV-EA activation...
Correlation between reduction potentials and inhibitions of Epstein-Barr virus activation by anthraquinone derivativesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Bioorg Med Chem Lett 18:4106-9. 2008..It was further shown that the correlation could be enhanced by including LUMO energy and the number of hydroxy groups as additional parameters...
Development of an LC-ESI-MS/MS method for the determination of histamine: application to the quantitative measurement of histamine degranulation by KU812 cellsJunko Koyama
Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
J Chromatogr B Analyt Technol Biomed Life Sci 877:207-12. 2009..Of these compounds, taxiresinol and isotaxiresinol were more inhibitory than sodium cromoglicate...
Characterization of emodin metabolites in Raji cells by LC-APCI-MS/MSJunko Koyama
Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Bioorg Med Chem 17:7493-9. 2009..In addition to the major metabolite 8-O-methylemodin, four other metabolites were assigned as omega-hydroxyemodin, 3-O-methyl-omega-hydroxyemodin, 3-O-methylemodin (physcion), and chrysophanol...
Correlation between cytotoxic activities and reduction potentials of heterocyclic quinonesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe, Japan
Molecules 15:6559-69. 2010..These results suggested that reduction-oxidation potentials could be a useful method for the discovery of novel antitumor agents...
Correlation of redox potentials and inhibitory effects on Epstein-Barr virus activation of 2-azaanthraquinonesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658 8558, Japan
Cancer Lett 212:1-6. 2004..It has been further shown that the correlation can be enhanced by introducing an electronic properties, i.e. the atomic charges at the C5 and O12 atoms in the quinone skeleton ring and the HOMO energy as additional parameters...
Correlation of redox potentials and inhibitory effects on Epstein-Barr virus activation of naphthoquinonesJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658, Japan
Cancer Lett 201:25-30. 2003..It has been further shown that the correlation can be enhanced by introducing an electronic property, i.e. the atomic charges at the C(4) and O(10) atoms in the quinone skeleton ring as additional parameters...
Capillary electrophoresis for simultaneous determination of emodin, chrysophanol, and their 8-beta-D-glucosidesJunko Koyama
Kobe Pharmaceutical University, Higashinada ku, Japan
Chem Pharm Bull (Tokyo) 51:418-20. 2003..The running electrolyte used in this method was 0.005 M alpha-cyclodextrin in 0.03 M borate buffer (pH 10.5) containing 10% acetonitrile, with an applied voltage of 20 kV...
Micellar electrokinetic chromatography (MEKC) separation of furanonaphthoquinones from Tabebuia impetiginosaJ Koyama
Kobe Pharmaceutical University, Japan
Chem Pharm Bull (Tokyo) 48:873-5. 2000....
Enantiomeric separation by cyclodextrin modified capillary zone electrophoresis (CD-CZE) of quaternary tetrahydroprotoberberine alkaloidsJ Koyama
Kobe Pharmaceutical University, Japan
Chem Pharm Bull (Tokyo) 48:1790-2. 2000..5 or 3) containing 10% acetonitrile with an applied voltage of 20 kV. This method was applied toward the enantioselective bio-conversion of quaternary tetrahydroprotoberberine N-metho salts in cultured cells of Corydalis species...
Bianthraquinones from Cassia siameaJ Koyama
Kobe Pharmaceutical University, Japan
Phytochemistry 56:849-51. 2001..The structures were established by analysis of spectroscopic data and 7-chloro-1,1',6,8,8'-pentahydroxy-3,3'-dimethyl[2,2'-bianthracene]-9,9',10,10'-tetrone was determined on the direct comparison with synthetic compound...
Inhibitory effects of anthraquinones and bianthraquinones on Epstein-Barr virus activationJ Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, 658, Kobe, Japan
Cancer Lett 170:15-8. 2001..Anthraquinone monomers showed higher anti-tumor promoting activity than that of bianthraquinones...
Correlation with redox potentials and inhibitory effects on Epstein-Barr virus activation of azaanthraquinonesJ Koyama
Kobe Pharmaceutical University, Higashinada, Japan
Chem Pharm Bull (Tokyo) 49:1214-6. 2001..It has further been shown that the correlation can be made better by introducing an electronic property, i.e., the atomic charge at O11 as an additional parameter...
Chemopreventive effects of emodin and cassiamin B in mouse skin carcinogenesisJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada, Kobe 658, Japan
Cancer Lett 182:135-9. 2002....
Capillary electrophoresis of anthraquinones from Cassia siameaJunko Koyama
Kobe Pharmaceutical University, Kobe, Japan
Chem Pharm Bull (Tokyo) 50:1103-5. 2002..Application of this technique in the determination of the main bianthraquinones, cassiamin A and cassiamin B, of Cassia siamea is demonstrated in this paper...
Structure-activity relations of azafluorenone and azaanthraquinone as antimicrobial compoundsJunko Koyama
Faculty of Pharmaceutical Sciences, Kobe Pharmaceutical University, Higashinada ku, Kobe 658 8558, Japan
Bioorg Med Chem Lett 15:1079-82. 2005..In addition, correlations among reduction potential, hydrophobic parameter, and antimicrobial activity were discussed...
Biotransformation of phenolic tetrahydroprotoberberines in plant cell cultures followed by LC-NMR, LC-MS, and LC-CDKinuko Iwasa
Kobe Pharmaceutical University, 4 19 1 Motoyamakita, Higashinada ku, Kobe shi 658 8558, Japan
J Nat Prod 73:115-22. 2010..cordata and C. ochotensis var. raddeana, which was distinct from O-methylation in N. domestica, in which 7 was O-methylated at both C-11 and C-10. Stereoselective O-demethylation [(S)-5 to (S)-18] occurred in N. domestica...
Higher radical scavenging activities of polyphenolic antioxidants can be ascribed to chemical reactions following their oxidationHiroki Hotta
Department of Chemistry, Faculty of Science, Kobe University, Nada, Japan
Biochim Biophys Acta 1572:123-32. 2002..In this study, we have proposed a possible mechanism for the oxidation of polyphenols, in which the oxidizable -OH moieties are reproduced through an oxidative dimerization (or more highly polymerization)...
Mechanistic study of the oxidation of caffeic acid by digital simulation of cyclic voltammogramsHiroki Hotta
Department of Chemistry, Faculty of Science, Kobe University, Nada, Kobe 657-8501, Japan
Anal Biochem 303:66-72. 2002..Evaluations of the rate constants for the chemical reactions have further suggested that the chemical reactions are dimerization reactions...
Paraquat detoxicative system in the mouse liver postmitochondrial fractionHiroki Shimada
Department of Anatomy, Kanazawa Medical University, Uchinada, Ishikawa 920 0293, Japan
Arch Biochem Biophys 402:149-57. 2002....
A new quassinoid, ailantinol H, from Ailanthus altissimaSadaaki Tamura
Faculty of Integrated Arts and Sciences, Hiroshima University, 1 7 1 Kagamiyama, Higashi hiroshima 739 8521, Japan
Nat Prod Res 20:1211-5. 2006..A new quassinoid, ailantinol H, was isolated from the aerial parts of Ailanthus altissima. The structure was elucidated based on spectral evidence...
Furanonaphthoquinones cause apoptosis of cancer cells by inducing the production of reactive oxygen species by the mitochondrial voltage-dependent anion channelEriko Simamura
Molecular and Cell Structural Science, Kanazawa Medical University, Uchinada, Ishikawa, Japan
Cancer Biol Ther 5:1523-9. 2006..These results indicate that the anticancer activity of furanonaphthoquinones depends on the production of reactive oxygen species by mitochondrial permeability transition pores including the VDAC...
Mitochondrial damage prior to apoptosis in furanonaphthoquinone treated lung cancer cellsEriko Simamura
Department of Anatomy, Kanazawa Medical University, Uchinada, Ishikawa 920 0293, Japan
Cancer Detect Prev 27:5-13. 2003..The higher dose of 5 microg/ml induced necrosis via severe mitochondrial breakage. These results showed that FNQ3 targets the mitochondria of A549 cells to produce a reactive oxygen species resulting in apoptosis and necrosis...
Three new quassinoids, ailantinol E, F, and G, from Ailanthus altissimaSadaaki Tamura
Faculty of Integrated Arts and Sciences, Hiroshima University, 1 7 1 Kagamiyama, Higashi hiroshima 739 8521, Japan
Chem Pharm Bull (Tokyo) 51:385-9. 2003..The new quassinoids were found to show potent activity without showing any cytotoxicity. The screening for inhibitors against nitric oxide donor action was also conducted using the new quassinoids and some standard samples...
