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Volumn 1, Issue 2, 2008, Pages 81-84

Neo-clerodane diterpenes from Ajuga turkestanica

Author keywords

14,15 Dihydroajugachin B; 14 Hydro 15 methoxyajugachin B; Ajuga turkestanica; Labiatae; Neo clerodane diterpenes

Indexed keywords

14 HYDRO 15 METHOXYAJUGACHIN B; 14,15 DIHYDROAJUGACHIN B; ACETIC ACID ETHYL ESTER; AJUGACHIN B; AJUGAPITIN; CHAMAEPITIN; CLERODANE DERIVATIVE; DITERPENE; DITERPENOID; LUPULIN A; PLANT EXTRACT;

EID: 48049090955     PISSN: 18743900     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytol.2008.03.004     Document Type: Article
Times cited : (19)

References (21)
  • 2
    • 0034559882 scopus 로고    scopus 로고
    • Phytoecdysteroids: structure, sources, and biosynthesis in plants
    • Baltaev U.A. Phytoecdysteroids: structure, sources, and biosynthesis in plants. Russ. J. Bioorg. Chem. 26 (2000) 799-831
    • (2000) Russ. J. Bioorg. Chem. , vol.26 , pp. 799-831
    • Baltaev, U.A.1
  • 3
    • 37049042103 scopus 로고
    • Diterpenoid bitter principles. Part III. The constitution of clerodin
    • Barton D.H.R., Cheng H.T., Cross A.D., and Jackman L.M. Diterpenoid bitter principles. Part III. The constitution of clerodin. J. Chem. Soc. (1961) 5061-5073
    • (1961) J. Chem. Soc. , pp. 5061-5073
    • Barton, D.H.R.1    Cheng, H.T.2    Cross, A.D.3    Jackman, L.M.4
  • 4
    • 0034175886 scopus 로고    scopus 로고
    • Responses of Spodoptera littoralis larvae to Tunisian plant extracts and to neo-clerodane diterpenoids isolated from Ajuga pseudoiva leaves
    • Ben Jannet H., Harzalla-Skhiri F., Mighri Z., Simmonds M.S.J., and Blaney W.M. Responses of Spodoptera littoralis larvae to Tunisian plant extracts and to neo-clerodane diterpenoids isolated from Ajuga pseudoiva leaves. Fitoterapia 71 (2000) 105-112
    • (2000) Fitoterapia , vol.71 , pp. 105-112
    • Ben Jannet, H.1    Harzalla-Skhiri, F.2    Mighri, Z.3    Simmonds, M.S.J.4    Blaney, W.M.5
  • 7
    • 0001375790 scopus 로고
    • Insect allelochemicals from Ajuga plants
    • Camps F., and Coll J. Insect allelochemicals from Ajuga plants. Phytochemistry 32 (1993) 1361-1370
    • (1993) Phytochemistry , vol.32 , pp. 1361-1370
    • Camps, F.1    Coll, J.2
  • 8
    • 9444231182 scopus 로고    scopus 로고
    • Antibacterial neoclerodane diterpenoids from Ajuga lupulina
    • Chen H., Tan R.X., Liu Z.L., and Zhang Y. Antibacterial neoclerodane diterpenoids from Ajuga lupulina. J. Nat. Prod. 59 (1996) 668-670
    • (1996) J. Nat. Prod. , vol.59 , pp. 668-670
    • Chen, H.1    Tan, R.X.2    Liu, Z.L.3    Zhang, Y.4
  • 10
    • 36849007431 scopus 로고    scopus 로고
    • Neo-clerodane diterpenoids from Ajuga: structural elucidation and biological activity
    • Coll J., and Tandron Y.A. Neo-clerodane diterpenoids from Ajuga: structural elucidation and biological activity. Phytochem. Rev. 7 (2008) 25-49
    • (2008) Phytochem. Rev. , vol.7 , pp. 25-49
    • Coll, J.1    Tandron, Y.A.2
  • 11
    • 0002078399 scopus 로고
    • A global survey of the biogeography of the Labiatae
    • Harley R.M., and Reynolds T. (Eds), Royal Botanic Gardens, Kew, Richmond, Surrey, UK
    • Hedge I.C. A global survey of the biogeography of the Labiatae. In: Harley R.M., and Reynolds T. (Eds). Advances in Labiate Science (1992), Royal Botanic Gardens, Kew, Richmond, Surrey, UK 7-17
    • (1992) Advances in Labiate Science , pp. 7-17
    • Hedge, I.C.1
  • 12
    • 0001146440 scopus 로고
    • Diterpenoids from Ajuga chamaepitys: two neo-clerodane derivatives
    • Hernandez A., Pascual C., Sanz J., and Rodríguez B. Diterpenoids from Ajuga chamaepitys: two neo-clerodane derivatives. Phytochemistry 21 (1982) 2909-2911
    • (1982) Phytochemistry , vol.21 , pp. 2909-2911
    • Hernandez, A.1    Pascual, C.2    Sanz, J.3    Rodríguez, B.4
  • 13
    • 0036899026 scopus 로고    scopus 로고
    • Insect antifeedant activity of clerodane diterpenes and related model compounds
    • Klein Gebbinck E.A., Jansen B.J.M., and de Groot A. Insect antifeedant activity of clerodane diterpenes and related model compounds. Phytochemistry 61 (2002) 737-770
    • (2002) Phytochemistry , vol.61 , pp. 737-770
    • Klein Gebbinck, E.A.1    Jansen, B.J.M.2    de Groot, A.3
  • 14
    • 0034739330 scopus 로고    scopus 로고
    • Cancer chemopreventive activity of an iridoid glycoside, 8-acetylharpagide, from Ajuga decumbens
    • Konoshima T., Takasaki M., Tokuda H., and Nishino H. Cancer chemopreventive activity of an iridoid glycoside, 8-acetylharpagide, from Ajuga decumbens. Cancer Lett. 157 (2000) 87-92
    • (2000) Cancer Lett. , vol.157 , pp. 87-92
    • Konoshima, T.1    Takasaki, M.2    Tokuda, H.3    Nishino, H.4
  • 15
    • 0032257949 scopus 로고    scopus 로고
    • Isolation of turkesterone from the epigeal part of Ajuga turkestanica and its anabolic activity
    • Mamatkhanov A.U., Yakubova M.R., and Syrov V.N. Isolation of turkesterone from the epigeal part of Ajuga turkestanica and its anabolic activity. Chem. Nat. Compd. 34 (1998) 150-154
    • (1998) Chem. Nat. Compd. , vol.34 , pp. 150-154
    • Mamatkhanov, A.U.1    Yakubova, M.R.2    Syrov, V.N.3
  • 16
    • 27744484669 scopus 로고    scopus 로고
    • Phytoecdysteroids and other biologically active compounds from plants of the genus Ajuga
    • Ramazanov N.S. Phytoecdysteroids and other biologically active compounds from plants of the genus Ajuga. Chem. Nat. Compd. 41 (2005) 361-369
    • (2005) Chem. Nat. Compd. , vol.41 , pp. 361-369
    • Ramazanov, N.S.1
  • 17
    • 4444251636 scopus 로고    scopus 로고
    • Assigning the C-15 configuration of 15-hydroxy-, 15-methoxy-, 15-ethoxy-hexahydrofurofuran neoclerodane diterpenoids
    • Rosselli S., Maggio A., Piozzi F., and Bruno M. Assigning the C-15 configuration of 15-hydroxy-, 15-methoxy-, 15-ethoxy-hexahydrofurofuran neoclerodane diterpenoids. Tetrahedron 60 (2004) 8791-8800
    • (2004) Tetrahedron , vol.60 , pp. 8791-8800
    • Rosselli, S.1    Maggio, A.2    Piozzi, F.3    Bruno, M.4
  • 21
    • 34250262004 scopus 로고
    • Phytoecdysones of Ajuga turkestanica VI. 22-Acetylcyasterone
    • Usmanov V.Z., Rashkes Y.V., and Abubakirov N.K. Phytoecdysones of Ajuga turkestanica VI. 22-Acetylcyasterone. Chem. Nat. Compd. 2 (1978) 215-219
    • (1978) Chem. Nat. Compd. , vol.2 , pp. 215-219
    • Usmanov, V.Z.1    Rashkes, Y.V.2    Abubakirov, N.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.