C. Yamagami

发表

Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. X. Relationship between Capacity Factor and Octanol-Water Partition Coefficients of Monosubstituted Thiophenes

C. Yamagami, Y. Masaki, 1995 .

Structure-activity relationship in potentially anti-tumor promoting benzalacetone derivatives, as assayed by the epstein-barr virus early antigen activation.

H. Nishino, Y. Saito, H. Tokuda, 2000, Mutation research.

Carbon‐13 NMR study of substituted benzyl N,N‐dimethylcarbamates

Y. Takeuchi, C. Yamagami, N. Takao, 1983 .

Quantitative structure-activity relationship studies for antioxidant hydroxybenzalacetones by quantum chemical- and 3-D-QSAR(CoMFA) analyses.

M. Akamatsu, T. Tanahashi, S. Hamada, 2005, Bioorganic & medicinal chemistry letters.

Quantitative structure-activity relationship analyses of antioxidant and free radical scavenging activities for hydroxybenzalacetones.

T. Tanahashi, Y. Takeuchi, N. Motohashi, 2004, Bioorganic & medicinal chemistry letters.

Inhibitory effects of dehydrozingerone and related compounds on 12-O-tetradecanoylphorbol-13-acetate induced Epstein-Barr virus early antigen activation.

H. Nishino, Y. Saito, T. Konoshima, 1998, Cancer letters.

Structure-antimutagenic activity relationships of benzalacetone derivatives against UV-induced mutagenesis in E. coli WP2uvrA and gamma-induced mutagenesis in Salmonella typhimurium TA2638.

Y. Saito, N. Motohashi, Y. Ashihara, 2001, Mutation research.

Antioxidant effects of hydroxybenzalacetones on peroxynitrite-induced lipid peroxidation in red blood cell membrane ghost and SOS response in Salmonella typhimurium TA4107/pSK1002.

Yutaka Saito, N. Motohashi, A. Takahashi, 2005, Chemical & pharmaceutical bulletin.

Quantitative structure--activity relationships of antimutagenic benzalacetones and 1,1,1-trifluoro-4-phenyl-3-buten-2-ones.

N. Motohashi, C. Yamagami, 2002, European journal of medicinal chemistry.

Hydrophobic Properties of Antimutagenic Benzalacetones and Related Compounds

N. Motohashi, C. Yamagami, Nami Kishida, 1998 .

Antimutagenic effects of dehydrozingerone and its analogs on UV-induced mutagenesis in Escherichia coli.

Y. Saito, N. Motohashi, Y. Ashihara, 1997, Mutation research.

Hydrophobicity parameters determined by reversed-phase liquid chromatography. VII: Hydrogen-bond effects in prediction of the log P values for benzyl N,N-dimethylcarbamates

C. Yamagami, N. Takao, 1993 .

13C N.M.R. Spectra of ortho-Substituted Phenyl N,N-Dimethyl-Carbamates and N-Methyl Carbamates

C. Yamagami, N. Takao, T. Sai, 1987 .

Quantitative structure-activity relationships of anticonvulsant aralkyl and alkyl carbamates.

M. Tanaka, K. Horisaka, T. Fujita, 1985, Chemical & pharmaceutical bulletin.

A quantitative structure-activity study of anticonvulsant benzyl N,N-dimethylcarbamates.

J. Yamada, M. Tanaka, K. Horisaka, 1982, Chemical & pharmaceutical bulletin.

Effect of Pressure on the Rate of Solvolysis. Formolysis and Methanolysis of Secondary Alkyl Tosylates

K. Maruyama, C. Yamagami, A. Sera, 1973 .

Hydrophobicity parameters determined by reversed-phase liquid chromatography. XV: optimal conditions for prediction of log P(oct) by using RP-HPLC procedures.

C. Yamagami, Kaname Kawase, K. Iwaki, 2002, Chemical & pharmaceutical bulletin.

Hydrophobicity parameters determined by reversed-phase liquid chromatography

Chisako Yamagami, Tamaki Ogura, Narao Takao, 1990 .

Hydrogen-bonding abilities for phenols assessed by quantitative analyses of their partition coefficients derived from different partitioning systems.

T. Tanahashi, Chisako Yamagami, Akira Hamasaki, 2005, Chemical & pharmaceutical bulletin.

Hydrophobicity parameters determined by reversed-phase liquid chromatography. XVI: A new hydrogen-accepting parameter for monosubstituted thiophenes and furans for correlating retention factors and octanol-water partition coefficients.

C. Yamagami, Hiromichi Tachikawa, 2003, Chemical & pharmaceutical bulletin.

A quantitative structure-activity study of anticonvulsant phenylacetanilides.

T. Fujita, M. Tanaka, K. Horisaka, 1984, Chemical & pharmaceutical bulletin.

Effect of Pressure on the Rate of Solvolysis. Volume Parameters and Solvolysis Mechanism

K. Maruyama, C. Yamagami, A. Sera, 1974 .

ORGANIC REACTION UNDER HIGH PRESSURE PART 14, EFFECT OF PRESSURE ON THE RATE OF SOLVOLYSIS, VOLUME PARAMETERS AND SOLVOLYSIS MECHANISM

K. Maruyama, C. Yamagami, A. Sera, 1974 .

EFFECT OF PRESSURE ON THE RATE OF SOLVOLYSIS. FORMOLYSIS OF 1-(P-SUBSTITUTED BENZYL)ETHYL TOSYLATES

C. Yamagami, A. Sera, 1972 .

Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. XI. Prediction of log P Values for Phenyl N-Methyl and Phenyl N, N-Dimethylcarbamates

C. Yamagami, Noriko Katashiba, 1996 .

Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. IX. Relationship between Capacity Factor and Water-Octanol Partition Coefficient of Monosubstituted Pyrimidines.

Mihoko Yokota, C. Yamagami, N. Takao, 1994 .

Application of a stepwise flow ratiometry without phase separation to the determination of the chloroform/water distribution coefficients of volatile diazines.

H. Chuman, Hideji Tanaka, Daichi Kawabata, 2005, Chemical & pharmaceutical bulletin.

Hydrophobicity parameter of diazines IV: a new hydrogen-accepting parameter of monosubstituted (di)azines for the relationship of partition coefficients in different solvent systems.

T. Fujita, C. Yamagami, 2000, Journal of pharmaceutical sciences.

Analysis and prediction of 1-octanol/water partition coefficients of substituted diazines with substituent and structural parameters

T. Fujita, C. Yamagami, N. Takao, 1995 .

Hydrophobicity Parameter of Diazines (1) Analysis and Prediction of Partition Coefficients of Monosubstituted Diazines

Toshio Fujita, T. Fujita, Chisako Yamagami, 1990 .

Kinetic studies of fast equilibrium by means of high-performance liquid chromatography. XIV. Separation of rotamers of phenyl methylcarbamates and their rotational energy barriers.

A. Kato, M. Moriyasu, Y. Hashimoto, 1986 .

13C NMR spectra of p- and m-substituted phenyl N-methyl- and phenyl N,N-dimethyl-carbamates

T. Fujita, T. Nishioka, Y. Takeuchi, 1984 .

Hydrophobic properties of anticonvulsant phenylacetanilides. Relationship between octanol-water partition coefficient and capacity factor determined by reversed-phase liquid chromatography.

K. Yamamoto, K Yamamoto, C Yamagami, 1984, Chemical & pharmaceutical bulletin.

Hydrophobicity Parameters Determined by Reversed‐Phase Liquid Chromatography. XIII A New Hydrogen‐accepting Scale of Monosubstituted (Di)azines for the Relationship between Retention Factor and Octanol‐Water Partition Coefficient

T. Fujita, C. Yamagami, Kaname Kawase, 1999 .

Hydrophobicity parameter of diazines. II: Analysis and prediction of partition coefficients of disubstituted pyrazines.

T. Fujita, C. Yamagami, N. Takao, 1991, Journal of pharmaceutical sciences.

Quantum chemical- and 3-D-QSAR (CoMFA) studies of benzalacetones and 1,1,1-trifluoro-4-phenyl-3-buten-2-ones.

M. Akamatsu, N. Motohashi, C. Yamagami, 2002, Bioorganic & medicinal chemistry letters.

Behavior of Hydrochlorides and Methiodides of N-Substituted 4-Piperidones in Methanol

M. Sugiura, C. Yamagami, N. Takao, 1980 .

Analyses of the partition coefficient, log P, using ab initio MO parameter and accessible surface area of solute molecules.

Toshio Fujita, Hiroshi Chuman, Atsushi Mori, 2004, Journal of pharmaceutical sciences.