Masami Ishibashi

Prof. Masami Ishibashi


Research Focus & Metrics

Academic Career Length

44Years (1983-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 1993 in Chemical Reviews
Verified
Journal Article
Closed access
JKJunichi. Kobayashi
Junichi. Kobayashi
MIMasami Ishibashi
Masami Ishibashi

1 December 1986 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
MIMasami Ishibashi
Masami Ishibashi
RMRichard E. Moore
Richard E. Moore
GPGregory M. L. Patterson
Gregory M. L. Patterson
CXChangfu Xu
Changfu Xu
JCJon Clardy
Jon Clardy

1 August 1991 in Tetrahedron
Verified
Journal Article
Closed access
JKJun'Ichi Kobayashi
Jun'Ichi Kobayashi
MTMasashi Tsuda
Masashi Tsuda
KAKaori Agemi
Kaori Agemi
HSHideyuki Shigemori
Hideyuki Shigemori
MIMasami Ishibashi
Masami Ishibashi
YMYuzuru Mikami
Yuzuru Mikami

1 April 1992 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
KKKazuhiko Kondo
Kazuhiko Kondo
HSHideyuki Shigemori
Hideyuki Shigemori
YKYumiko Kikuchi
Yumiko Kikuchi
MIMasami Ishibashi
Masami Ishibashi
TSTakuma Sasaki
Takuma Sasaki
JKJunichi Kobayashi
Junichi Kobayashi

1 January 2001 in Chemical and Pharmaceutical Bulletin
Verified
Journal Article
Closed access
EOEmi Okuyama
Emi Okuyama
THTetsuya Hasegawa
Tetsuya Hasegawa
TMTakamitsu Matsushita
Takamitsu Matsushita
HFHaruhiro Fujimoto
Haruhiro Fujimoto
MIMasami Ishibashi
Masami Ishibashi
MYMikio Yamazaki
Mikio Yamazaki
By activity-oriented separation using the writhing method in mice, the analgesic components of Saposhnikovia root (Saposhnikovia divaricata Schischkin; Umbelliferae) were identified to be chromones, coumarins, polyacetylenes and 1-acylglycerols. Two new components, divaricatol and (3'S)-hydroxydeltoin, were also isolated. The most potent analgesia was observed in chromones such as divaricatol, ledebouriellol and hamaudol, which inhibited writhing inhibition at an oral dose of 1 mg/kg in mice. Acylglycerols also showed inhibition significantly at a dose of 5 mg/kg. In some pharmacological tests using sec-O-glucosylhamaudol, the compound showed analgesia by the tail pressure and the Randall & Selitto methods, and its writhing inhibition was not reversed by naloxone.

28 April 2008 in ChemBioChem
Verified
Journal Article
Closed access
PDF file
THTakahiro Hosoya
Takahiro Hosoya
MAMidori A. Arai
Midori A. Arai
TKTakashi Koyano
Takashi Koyano
TKThaworn Kowithayakorn
Thaworn Kowithayakorn
MIMasami Ishibashi
Masami Ishibashi