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Featured researches published by Ichiro Honda.


Cancer Letters | 1991

Inhibitory effects of 3-nitro-2,4,6-trihydroxybenzamides on Epstein-Barr virus early antigen induction

Ichiro Honda; Harukuni Tokuda; Mutsuo Kozuka; Koichi Yoneyama; Hoyoku Nishino; Akio Iwashima; Makoto Shibagaki; Masana Noma; Nobutaka Takahashi; Shigeo Yoshida

Inhibitory effects of a series of 3-nitro-2,4,6-trihydroxybenzamides on Epstein-Barr virus early antigen (EBV-EA) induction were examined using Raji cells. Some of the tested compounds showed highly inhibitory activity, the N-octyl amide derivative being the most active among them. These results suggest the possibility that 3-nitro-2,4,6-trihydroxybenzamides might be listed as novel inhibitors of tumor promotion.


Bulletin of the Chemical Society of Japan | 1991

Regioselective hydrogenation using platinum-support zeolite modified by CVD-method

Hideyuki Kuno; Makoto Shibagaki; Kyoko Takahashi; Ichiro Honda; Hajime Matsushita

Abstract Platinum-support zeolites coupled with silicon alkoxides were prepared by the Chemical Vapor Deposition (CVD) method. With this catalyst system, it was demonstrated that the terminal carbon-carbon double bond is preferentially hydrogenated in the case of several unsaturated hydrocarbons. Further, it was elucidated that highly regioselective hydrogenation of alkadiene could also be achieved in this catalyst system.


Cancer Letters | 1993

Inhibitory effects of 3-nitrophloroglucinecarboxylic acid derivatives on Epstein-Barr virus early antigen induction.

Ichiro Honda; Harukuni Tokuda; Mutsuo Kozuka; Koichi Yoneyama; Hoyoku Nishino; Akio Iwashima; Makoto Shibagaki; Masana Noma; Nobutaka Takahashi; Shigeo Yoshida

The inhibitory effects of two series of 3-nitrophloroglucinecarboxylic acid derivatives, 3-nitro-2,4,6-trihydroxythiobenzamides (II) and 3-nitro-phloroglucinecarboxylates (III), on Epstein-Barr virus early antigen (EBV-EA) induction were examined using Raji cells. Some of them strongly inhibited the induction, N-nonyl and O-decyl derivatives being the most potent inhibitors among the thioamides and esters, respectively. These results suggest the possibility that these two 3-nitrophloroglucinecarboxylic acid derivatives may be listed as novel inhibitors of tumor promotion.


Bulletin of the Chemical Society of Japan | 1969

t-Amyloxycarbonyl as a New Protecting Group in Peptide Synthesis. V. Direct Synthesis of t-Amyloxycarbonyl- and t-Butyloxycarbonyl-amino Acids Using the Respective t-Alkyl Chloroformates

Shumpei Sakakibara; Ichiro Honda; Katsumi Takada; Muneji Miyoshi; Takanobu Ohnishi; Kentaro Okumura


Bulletin of the Chemical Society of Japan | 1970

A New Protective Group Suitable for Masking Specific Amino Groups during Peptide Synthesis

Shumpei Sakakibara; Tsunehiko Fukuda; Yasuo Kishida; Ichiro Honda


Japanese Journal of Pharmacology | 1977

SPECIFIC PRESSOR ACTIVITY AND STABILITY OF SYNTHETIC ANGIOTENSINS

Takushi X. Watanabe; Hirofumi Sokabe; Ichiro Honda; Shumpei Sakakibara; Taeko Nakayama; Terumi Nakajima


Agricultural and biological chemistry | 1990

Structure—Activity Relationship of 3-Nitro-2,4,6-trihydroxybenzamide Derivatives in Photosynthetic Electron Transport Inhibition

Ichiro Honda; Koichi Yoneyama; Hajime Iwamura; Makoto Konnai; Nobutaka Takahashi; Shigeo Yoshida


Bulletin of the Chemical Society of Japan | 1967

t-Amyloxycarbonyl as a new protecting group in peptide synthesis. IV. Synthesis and use of t-amyl azidoformate.

Ichiro Honda; Yasutsugu Shimonishi; Shumpei Sakakibara


Chemistry Letters | 1992

Lactonization of ω-Hydroxy Esters over Hydrous Zirconium(IV) Oxide

Hideyuki Kuno; Makoto Shibagaki; Kyoko Takahashi; Ichiro Honda; Hajime Matsushita


Agricultural and biological chemistry | 1990

Syntheses of 3-Nitro-2,4,6-trihydroxybenzamide and Thiobenzamide Derivatives as Highly Potent Inhibitors of Photosynthetic Electron Transport

Ichiro Honda; Koichi Yoneyama; Makoto Konnai; Nobutaka Takahashi; Shigeo Yoshida

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Akio Iwashima

Kyoto Prefectural University of Medicine

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