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Published in: Journal of Natural Medicines 4/2016

01-10-2016 | Note

Dianthosaponins G–I, triterpene saponins, an anthranilic acid amide glucoside and a flavonoid glycoside from the aerial parts of Dianthus japonicus and their cytotoxicity

Authors: Yuka Kanehira, Susumu Kawakami, Sachiko Sugimoto, Katsuyoshi Matsunami, Hideaki Otsuka

Published in: Journal of Natural Medicines | Issue 4/2016

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Abstract

Extensive isolation work on the 1-BuOH-soluble fraction of a MeOH extract of the aerial parts of Dianthus japonicus afforded three further triterpene glycosyl estsers, termed dianthosaponins G–I, an anthranilic acid amide glucoside and a C-glycosyl flavonoid along with one known triterpene saponin. Their structures were elucidated from spectroscopic evidence. The cytotoxicity of the isolated compounds toward A549 cells was evaluated.
Literature
1.
go back to reference Nakano T, Sugimoto S, Matsunami K, Otsuka H (2011) Dianthosaponins A–F, triterpene saponins, flavonoid glycoside, aromatic amide glucoside and γ-pyrone glucoside from Dianthus japonicus. Chem Pharm Bull 59:1141–1148CrossRefPubMed Nakano T, Sugimoto S, Matsunami K, Otsuka H (2011) Dianthosaponins A–F, triterpene saponins, flavonoid glycoside, aromatic amide glucoside and γ-pyrone glucoside from Dianthus japonicus. Chem Pharm Bull 59:1141–1148CrossRefPubMed
2.
go back to reference Oshima Y, Ohsawa H, Hikino H (1984) Structures of dianosides G, H and I, triterpenoid saponins of Dianthus superbus var. longicalycinus herbs. Planta Med 80:254–258CrossRef Oshima Y, Ohsawa H, Hikino H (1984) Structures of dianosides G, H and I, triterpenoid saponins of Dianthus superbus var. longicalycinus herbs. Planta Med 80:254–258CrossRef
3.
go back to reference Park S-Y, Yook C-S, Nohara T (2005) New oleanene glycosides from the leaves of Acanthopanax japonicus. Chem Pharm Bull 53:1147–1151CrossRefPubMed Park S-Y, Yook C-S, Nohara T (2005) New oleanene glycosides from the leaves of Acanthopanax japonicus. Chem Pharm Bull 53:1147–1151CrossRefPubMed
4.
go back to reference Koike K, Jia Z, Nikaido H (1999) New triterpenoid saponins and sapogenins from Saponaria officinalis. J Nat Prod 62:1655–1659CrossRefPubMed Koike K, Jia Z, Nikaido H (1999) New triterpenoid saponins and sapogenins from Saponaria officinalis. J Nat Prod 62:1655–1659CrossRefPubMed
5.
go back to reference Li H-Y, Koike K, Ohmoto T (1994) Triterpenoid saponins from Dianthus chinensis. Phytochemistry 35:751–756CrossRefPubMed Li H-Y, Koike K, Ohmoto T (1994) Triterpenoid saponins from Dianthus chinensis. Phytochemistry 35:751–756CrossRefPubMed
6.
go back to reference Ma L, Gu Y-C, Luo J-G, Wang J-S, Huang X-F, Kong L-Y (2009) Triterpenoid saponins from Dianthus versicolor. J Nat Prod 72:640–644CrossRefPubMed Ma L, Gu Y-C, Luo J-G, Wang J-S, Huang X-F, Kong L-Y (2009) Triterpenoid saponins from Dianthus versicolor. J Nat Prod 72:640–644CrossRefPubMed
7.
go back to reference Koike K, Jia Z, Nikaido T (1998) Triterpenoid saponins from Vaccaria segetalis. Phytochemistry 47:1343–1349CrossRefPubMed Koike K, Jia Z, Nikaido T (1998) Triterpenoid saponins from Vaccaria segetalis. Phytochemistry 47:1343–1349CrossRefPubMed
8.
go back to reference Davoust D, Massias M, Molho D (1980) Carbon-13 NMR investigation of flavonoid C-β-glucosides. Detection of a conformational equilibrium. Org Magn Reson 13:218–219CrossRef Davoust D, Massias M, Molho D (1980) Carbon-13 NMR investigation of flavonoid C-β-glucosides. Detection of a conformational equilibrium. Org Magn Reson 13:218–219CrossRef
Metadata
Title
Dianthosaponins G–I, triterpene saponins, an anthranilic acid amide glucoside and a flavonoid glycoside from the aerial parts of Dianthus japonicus and their cytotoxicity
Authors
Yuka Kanehira
Susumu Kawakami
Sachiko Sugimoto
Katsuyoshi Matsunami
Hideaki Otsuka
Publication date
01-10-2016
Publisher
Springer Japan
Published in
Journal of Natural Medicines / Issue 4/2016
Print ISSN: 1340-3443
Electronic ISSN: 1861-0293
DOI
https://doi.org/10.1007/s11418-016-1019-8

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