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

Toshiro NoshitaFaculty of Life and Environmental Sciences, Department of Life Sciences, Prefectural University of Hiroshima, Hiroshima, Japan;Program in Biological System Sciences, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, HiroshimaJapanCorrespondence[email protected]

Akihiro TaiFaculty of Life and Environmental Sciences, Department of Life Sciences, Prefectural University of Hiroshima, Hiroshima, Japan;Program in Biological System Sciences, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, HiroshimaJapan

Hikaru NishikawaProgram in Biological System Sciences, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, HiroshimaJapan

Kaoru IkedaProgram in Biological System Sciences, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, HiroshimaJapan

Hidekazu OuchiFaculty of Pharmaceutical Education, Department of Pharmacy, Kinki University, Osaka, Japan

Yoshitomo HamadaGraduate School of Engineering, Osaka Electro-Communication University, OsakaJapan

Akiko SaitoGraduate School of Engineering, Osaka Electro-Communication University, OsakaJapan

Teiko YamadaDepartment of Bioscience and Biotechnology for Future Bioindustry, Graduate School of Agricultural Science, Tohoku University, SendaiJapan

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

Table 1. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol G (CD₃OD, 500/125 MHz).

Table 2. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol B (CD₃OD, 500/125 MHz).

Table 3. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol C (CDCl_3, 500/125 MHz).

Table 4. Comparison of chemical shifts of 7- and 7ʹ-aldehyde and methoxy group.Table Footnote^a

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

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Table 1. 1H and 13C NMR dataTable Footnotea for synthesized and reported apteniol G (CD3OD, 500/125 MHz).

Table 2. 1H and 13C NMR dataTable Footnotea for synthesized and reported apteniol B (CD3OD, 500/125 MHz).

Table 3. 1H and 13C NMR dataTable Footnotea for synthesized and reported apteniol C (CDCl3, 500/125 MHz).

Table 4. Comparison of chemical shifts of 7- and 7ʹ-aldehyde and methoxy group.Table Footnotea

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Table 1. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol G (CD₃OD, 500/125 MHz).

Table 2. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol B (CD₃OD, 500/125 MHz).

Table 3. ¹H and ¹³C NMR dataTable Footnote^a for synthesized and reported apteniol C (CDCl_3, 500/125 MHz).

Table 4. Comparison of chemical shifts of 7- and 7ʹ-aldehyde and methoxy group.Table Footnote^a