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

Author:

Noshita Toshiro12,Tai Akihiro12,Nishikawa Hikaru2,Ikeda Kaoru2,Ouchi Hidekazu3,Hamada Yoshitomo4,Saito Akiko4,Yamada Teiko5

Affiliation:

1. Faculty of Life and Environmental Sciences, Department of Life Sciences, Prefectural University of Hiroshima, Hiroshima, Japan

2. Program in Biological System Sciences, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, Hiroshima Japan

3. Faculty of Pharmaceutical Education, Department of Pharmacy, Kinki University, Osaka, Japan

4. Graduate School of Engineering, Osaka Electro-Communication University, Osaka Japan

5. Department of Bioscience and Biotechnology for Future Bioindustry, Graduate School of Agricultural Science, Tohoku University, Sendai Japan

Abstract

Abstract The synthesis of compounds with the structures proposed for the oxyneolignan apteniols B, C, and G is described. The diphenyl ether skeletons of the proposed apteniols were formed via Ullmann ether synthesis. In particular, the spectral data for the synthesized apteniols B, C, and G did not agree with those previously reported for the isolated compounds. Furthermore, the synthesized proposed apteniol B did not show degranulation-inhibiting activity, while the prepared proposed apteniols C and G exhibited activities considerably weaker than that of the methyl ester of proposed apteniol A.

Funder

Sasakawa Scientific Research Grant from the Japan Science Society and BRAIN

Technology Research Promotion Program for Agriculture, Forestry, Fisheries, and Food Industry

Program for the Promotion of Basic and Applied Research for Innovations in Bio-oriented Industry

Publisher

Oxford University Press (OUP)

Subject

Organic Chemistry,Molecular Biology,Applied Microbiology and Biotechnology,General Medicine,Biochemistry,Analytical Chemistry,Biotechnology

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