Saponin and Sapogenol. XLII. : Structures of Acetyl-soyasaponins A1, A2, and A3, Astringent Partially Acetylated Bisdesmosides of Soyasapogenol A, from American Soybean, the Seeds of Glycine max MERRILL

By means of high performance liquid chromatography and other methods, three new partially acetylated soyasaponins, named acetyl-soyasaponin A1 (6a), acetyl-soyasaponin A2 (7a), and acetyl-soyasaponin A3 (8a), were isolated from American soybeans, the seeds of Glycine max MERRILL., together with hith...

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Veröffentlicht in:Chemical & pharmaceutical bulletin 1988/08/25, Vol.36(8), pp.2819-2828
Hauptverfasser: KITAGAWA, ISAO, TANIYAMA, TOSHIO, NAGAHAMA, YOSHIKO, OKUBO, KAZUYOSHI, YAMAUCHI, FUMIO, YOSHIKAWA, MASAYUKI
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container_end_page 2828
container_issue 8
container_start_page 2819
container_title Chemical & pharmaceutical bulletin
container_volume 36
creator KITAGAWA, ISAO
TANIYAMA, TOSHIO
NAGAHAMA, YOSHIKO
OKUBO, KAZUYOSHI
YAMAUCHI, FUMIO
YOSHIKAWA, MASAYUKI
description By means of high performance liquid chromatography and other methods, three new partially acetylated soyasaponins, named acetyl-soyasaponin A1 (6a), acetyl-soyasaponin A2 (7a), and acetyl-soyasaponin A3 (8a), were isolated from American soybeans, the seeds of Glycine max MERRILL., together with hitherto known soyasaponins I (3), II (4), and III (5). Acetyl-soyasaponins A1, A2, and A3 are noteworthy due to their bitter and astringent tastes, although their parent saponins, soyasaponins A1 (6), A2 (7), and A3 (8), do not show such tastes.By virtue of the photochemical degradation method for the glucuronide linkage and on the basis of 1H- and 13C-nuclear magnetic resonance and secondary ion mass spectrum analyses, structures of acetyl-soyasaponins A1, A2, and A3 have been elucidated as 3-O-[β-D-glucopyranosyl-(1→2)-β-D-galactopyranosyl(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (6a), 3-O-[β-D-galactopyranosyl-(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (7a), and 3-O-[α-L-arabinopyranosyl(1→2)-β-D-glucuronopy-ranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soya-sapogenol A (8a), respectively.
doi_str_mv 10.1248/cpb.36.2819
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XLII. : Structures of Acetyl-soyasaponins A1, A2, and A3, Astringent Partially Acetylated Bisdesmosides of Soyasapogenol A, from American Soybean, the Seeds of Glycine max MERRILL</title><title>Chemical &amp; pharmaceutical bulletin</title><addtitle>Chem. Pharm. Bull.</addtitle><description>By means of high performance liquid chromatography and other methods, three new partially acetylated soyasaponins, named acetyl-soyasaponin A1 (6a), acetyl-soyasaponin A2 (7a), and acetyl-soyasaponin A3 (8a), were isolated from American soybeans, the seeds of Glycine max MERRILL., together with hitherto known soyasaponins I (3), II (4), and III (5). Acetyl-soyasaponins A1, A2, and A3 are noteworthy due to their bitter and astringent tastes, although their parent saponins, soyasaponins A1 (6), A2 (7), and A3 (8), do not show such tastes.By virtue of the photochemical degradation method for the glucuronide linkage and on the basis of 1H- and 13C-nuclear magnetic resonance and secondary ion mass spectrum analyses, structures of acetyl-soyasaponins A1, A2, and A3 have been elucidated as 3-O-[β-D-glucopyranosyl-(1→2)-β-D-galactopyranosyl(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (6a), 3-O-[β-D-galactopyranosyl-(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (7a), and 3-O-[α-L-arabinopyranosyl(1→2)-β-D-glucuronopy-ranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soya-sapogenol A (8a), respectively.</description><subject>glucuronide photolysis</subject><issn>0009-2363</issn><issn>1347-5223</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><recordid>eNpFkV1r2zAUhkXpoGm6q_2Bc9_Y04ct2b1zs7QLeGw0G-zOyPJJ62DLQVJh_ov9VY2T0N1IB87zPgK9hHxhNGY8yb6afR0LGfOM5RdkxkSiopRzcUlmlNI84kKKK3Lt_Y5SnlIlZuRto_eDbS1o28A0P6Mduhj-lut1DHewCe7VhFeHHoYtFAbD2EV-GLU_5TwUbAEFXxwFhTjMPrjWHjQBfmkXWt114zmoAzZw3_oGfT_4tjlJN2fb8WUoFrB1Qw9Fj6412k7rGrVdQHhB2CA2x9BjN5rWIvT6H_xYPT2ty_KGfNrqzuPn8z0nfx5Wv5ffo_Ln43pZlJFJEp5HQjOUMpUUleBZKmua53WdqLpRmRK1ZEIleZJq08hUK8rRZMIwwxlLMiGZEnNye_IaN3jvcFvtXdtrN1aMVlMN1aGGSshqquFAfzvROx_0M36w09eYDieW5Wk28edjiv1fv2hXoRXvalCSpw</recordid><startdate>1988</startdate><enddate>1988</enddate><creator>KITAGAWA, ISAO</creator><creator>TANIYAMA, TOSHIO</creator><creator>NAGAHAMA, YOSHIKO</creator><creator>OKUBO, KAZUYOSHI</creator><creator>YAMAUCHI, FUMIO</creator><creator>YOSHIKAWA, MASAYUKI</creator><general>The Pharmaceutical Society of Japan</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1988</creationdate><title>Saponin and Sapogenol. 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XLII. : Structures of Acetyl-soyasaponins A1, A2, and A3, Astringent Partially Acetylated Bisdesmosides of Soyasapogenol A, from American Soybean, the Seeds of Glycine max MERRILL</atitle><jtitle>Chemical &amp; pharmaceutical bulletin</jtitle><addtitle>Chem. Pharm. Bull.</addtitle><date>1988</date><risdate>1988</risdate><volume>36</volume><issue>8</issue><spage>2819</spage><epage>2828</epage><pages>2819-2828</pages><issn>0009-2363</issn><eissn>1347-5223</eissn><abstract>By means of high performance liquid chromatography and other methods, three new partially acetylated soyasaponins, named acetyl-soyasaponin A1 (6a), acetyl-soyasaponin A2 (7a), and acetyl-soyasaponin A3 (8a), were isolated from American soybeans, the seeds of Glycine max MERRILL., together with hitherto known soyasaponins I (3), II (4), and III (5). Acetyl-soyasaponins A1, A2, and A3 are noteworthy due to their bitter and astringent tastes, although their parent saponins, soyasaponins A1 (6), A2 (7), and A3 (8), do not show such tastes.By virtue of the photochemical degradation method for the glucuronide linkage and on the basis of 1H- and 13C-nuclear magnetic resonance and secondary ion mass spectrum analyses, structures of acetyl-soyasaponins A1, A2, and A3 have been elucidated as 3-O-[β-D-glucopyranosyl-(1→2)-β-D-galactopyranosyl(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (6a), 3-O-[β-D-galactopyranosyl-(1→2)-β-D-glucuronopyranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soyasapogenol A (7a), and 3-O-[α-L-arabinopyranosyl(1→2)-β-D-glucuronopy-ranosyl]-22-O-[2, 3, 4, 6-tetra-O-acetyl-β-D-glucopyranosyl(1→3)-α-L-arabinopyranosyl]soya-sapogenol A (8a), respectively.</abstract><pub>The Pharmaceutical Society of Japan</pub><doi>10.1248/cpb.36.2819</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects glucuronide photolysis
title Saponin and Sapogenol. XLII. : Structures of Acetyl-soyasaponins A1, A2, and A3, Astringent Partially Acetylated Bisdesmosides of Soyasapogenol A, from American Soybean, the Seeds of Glycine max MERRILL
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