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Constituents of Caryopteris incana and their antibacterial activity

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Abstract

Two new compounds named caryocanolide (1), and caryocanoside A (2), together with nine known compounds (3–11) were isolated from the whole plant of Caryopteris incana. These structures were determined mainly on the basis of 2D nuclear magnetic resonance and high resolution fast atom bombardment mass spectroscopy data. Furthermore, the isolated compounds (1, 2, 4–11) were tested for their antibacterial activity. Compound 1 exhibited moderate antimicrobial activity against Bacillus subtilis with a minimum inhibitory concentration value of 35.7 μM.

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References

  1. Tsukamoto Y (1988) The grand dictionary of Horticulture. Syogakukan, Tokyo

    Google Scholar 

  2. Makino T (1982) Makino’s illustrated flora in colour. Hokuryukan, Tokyo

    Google Scholar 

  3. Zhao DP, Matsumami K, Otsuka H (2009) Iridoid glucoside, (3R)-oct-1-en-3-ol glycosides, and phenylethanoid from the aerial parts of Caryopteris incana. J Nat Med 63:241–247

    Article  CAS  Google Scholar 

  4. Gao J, Igarashi K, Nukina M (2000) Three new phenylethanoid glycosides from Caryopteris incana and their antioxidative activity. Chem Pharm Bull 48:1075–1078

    Article  PubMed  CAS  Google Scholar 

  5. Gao J, Igarashi K, Nukina M (1999) Radical scavenging activity of phenylpropanoid glycosides in Caryopteris incana. Biosci Biotechnol Biochem 63:983–988

    Article  PubMed  CAS  Google Scholar 

  6. Gao J, Han G (1997) Cytotoxic abietane diterpenoids from Caryopteris incana. Phytochemistry 44:759–761

    Article  CAS  Google Scholar 

  7. Yoshikawa K, Itou T, Iseki K, Baba T, Imagawa H, Morita H, Kawano S, Asakawa Y, Hashimoto T (2012) Phenanthrene derivatives from Cymbidium Great Flower Marie Laurencin and their biological activities. J Nat Prod 51:767–769

    Google Scholar 

  8. Yoshikawa K, Kawahara Y, Arihara S, Hashimoto T (2011) Aromatic compounds and their biological antioxidant activity of Acer saccharum. J Nat Med 65:191–193

    Article  PubMed  CAS  Google Scholar 

  9. Yoshikawa K, Yagi C, Hama H, Tanaka M, Arihara S, Hashimoto T (2010) Ipomotaosides A-D, resin glycosides from the aerial parts of Ipomoea batatas and their inhibitory activity against COX-1 and COX-2. J Nat Prod 73:1763–1766

    Article  PubMed  CAS  Google Scholar 

  10. Phadnis AP, Patwardhan SA, Dhaneshwar NN, Tavale SS, Row TNG (1988) Clerodane diterpenoids from Polyalthia longifolia. Phytochemistry 27:2899–2901

    Article  CAS  Google Scholar 

  11. Hannedouche S, Jacquemond-Collet I, Fabre N, Stanislas E, Mouls C (1999) Iridoid keto-glycosides from Caryopteris × Clandonensis. Phytochemistry 51:767–769

    Article  CAS  Google Scholar 

  12. Yamamoto A, Nitta S, Miyase T, Ueno A, Wu L-J (1993) Phenylethanoid and lignan-iridoid complex glycosides from roots of Buddleja davidii. Phytochemistry 32:421–425

    Article  PubMed  CAS  Google Scholar 

  13. Suzuki N, Miyase T, Ueno A (1993) Phenylethanoid glycosides of Sesamum indicum. Phytochemistry 34:729–732

    Google Scholar 

  14. Calis I, Saracoglu I, Basaran AA, Sticher O (1993) Two phenethyl alcohol glycosides from Scutellaria orientalis subsp. Pinnatifida. Phytochemistry 32:1621–1623

    Article  PubMed  CAS  Google Scholar 

  15. Kijjoa A, Pinto MMM, Pinho PMM, Tantisewie B, Herz W (1990) Clerodane derivatives from Polyalthia viridis. Phytochemistry 29:653–655

    Article  CAS  Google Scholar 

  16. Singh P, Krishna V, Pareek RB (1998) Diterpenes derived from clerodane skeleton from some compositae plants. J Indian Chem Soc 75:552–558

    CAS  Google Scholar 

  17. Matsumoto K, Ebata T, Koseki K, Okano K, Kawakami H, Matsushita H (1993) A novel synthesis of 4-deoxy-d-lyxo-hexose (4-deoxy-d-mannose) from 1,6-anhydro-3,4-dideoxy-β-d-glycero-hex-3-enopyranose-2-ulose (levoglucose-none). Carbohydr Res 246:345–352

    Article  CAS  Google Scholar 

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Authors and Affiliations

  1. Faculty of Pharmaceutical Sciences, Tokushima Bunri University, Yamashiro-Cho, Tokushima, 770-8514, Japan

    Kazuko Yoshikawa, Akinori Harada, Kanako Iseki & Toshihiro Hashimoto

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  1. Kazuko Yoshikawa
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  2. Akinori Harada
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  3. Kanako Iseki
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  4. Toshihiro Hashimoto
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Correspondence to Kazuko Yoshikawa.

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Yoshikawa, K., Harada, A., Iseki, K. et al. Constituents of Caryopteris incana and their antibacterial activity. J Nat Med 68, 231–235 (2014). https://doi.org/10.1007/s11418-013-0785-9

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  • DOI: https://doi.org/10.1007/s11418-013-0785-9

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