scispace - formally typeset
H

Hidekazu Ouchi

Researcher at Kindai University

Publications -  8
Citations -  25

Hidekazu Ouchi is an academic researcher from Kindai University. The author has contributed to research in topics: Williamson ether synthesis & Moiety. The author has an hindex of 3, co-authored 8 publications receiving 21 citations.

Papers
More filters
Journal ArticleDOI

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

TL;DR: The structure–activity relationships of flavonoids in their degranulation-inhibiting activity have not been systematically characterized and the information obtained may guide the development of a therapy for type I allergies.
Journal ArticleDOI

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

TL;DR: The synthesis of compounds with the structures proposed for the oxyneolignan apteniols B, C, and G did not agree with those of isolated compounds and did not show degranulation-inhibiting activity.
Journal ArticleDOI

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

TL;DR: In this article, the synthesis of 3,5-dimethoxy-4-{2-methoxy]-4-[(1E)-3-oxoprop-1-en-1yl]benzaldehyde (1) (the proposed structure for the naturally occurring protein tyrosine phosphatase 1B) inhibitor isolated from Acanthopanax senticosus) and its three positional isomers 3, 4, and 5.
Journal ArticleDOI

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

TL;DR: The dimethyl ester derivative of the proposed apteniol A was found to enhance neurite outgrowth in PC12 cells and inhibit antigen-induced degranulation in RBL-2H3 cells.
Journal ArticleDOI

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

TL;DR: The synthesis of 4,4′-oxyneolignan, the proposed structure for naturally occurring apteniol D, was formed via classical Ullmann ether synthesis using excess copper powder in N,N-dimethylacetamide.