메뉴 건너뛰기




Volumn 69, Issue 6, 2008, Pages 1328-1338

Bioactive triterpene derivatives from latex of two Euphorbia species

Author keywords

Euphorbia; Insect growth regulation; Spodoptera littoralis; Triterpene

Indexed keywords

EUPHORBIA; EUPHORBIA OFFICINARUM; EUPHORBIA RESINIFERA; HEXAPODA; LACTUCA; LACTUCA SATIVA; MAMMALIA; MYZUS PERSICAE; RHOPALOSIPHUM PADI; SPODOPTERA LITTORALIS;

EID: 41049114971     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2008.01.004     Document Type: Article
Times cited : (58)

References (44)
  • 1
    • 41049106747 scopus 로고
    • Terpénoïdes-VI. Dégradation de la chaîne latérale de l'euphol
    • Auduin M., and Levisalles J. Terpénoïdes-VI. Dégradation de la chaîne latérale de l'euphol. Tetrahedron 39 (1983) 2799-2802
    • (1983) Tetrahedron , vol.39 , pp. 2799-2802
    • Auduin, M.1    Levisalles, J.2
  • 2
    • 0036180467 scopus 로고    scopus 로고
    • Eupha-7,9(11),24-trien-3β-ol ("Antiquol C") and other triterpenes from Euphorbia antiquorum latex and their inhibitory effects on Epstein-Barr virus activation
    • Akihisa T., Wijeratne K., Tokuda H., Enjo F., Toriumi M., Kimura Y., Koike K., Nikaido T., Tezuka Y., and Nishino H. Eupha-7,9(11),24-trien-3β-ol ("Antiquol C") and other triterpenes from Euphorbia antiquorum latex and their inhibitory effects on Epstein-Barr virus activation. J. Nat. Prod. 65 (2002) 158-162
    • (2002) J. Nat. Prod. , vol.65 , pp. 158-162
    • Akihisa, T.1    Wijeratne, K.2    Tokuda, H.3    Enjo, F.4    Toriumi, M.5    Kimura, Y.6    Koike, K.7    Nikaido, T.8    Tezuka, Y.9    Nishino, H.10
  • 3
    • 0031025655 scopus 로고    scopus 로고
    • Euphorbium: modern research on its active principle, resiniferatoxin, reviews an ancient medicine
    • Appendino G., and Szallasi A. Euphorbium: modern research on its active principle, resiniferatoxin, reviews an ancient medicine. Life Science 60 (1997) 681-696
    • (1997) Life Science , vol.60 , pp. 681-696
    • Appendino, G.1    Szallasi, A.2
  • 5
    • 3342886591 scopus 로고
    • 13C des quatre classes tétracycliques, eupho-lanostane, élémo-lanostane, lanostane et nor-31 lanostane
    • 13C des quatre classes tétracycliques, eupho-lanostane, élémo-lanostane, lanostane et nor-31 lanostane. Bull. Soc. Chim. Fr. 5 (1985) 965-972
    • (1985) Bull. Soc. Chim. Fr. , vol.5 , pp. 965-972
    • Benharref, A.1    Lavergne, J.P.2
  • 8
    • 26444484530 scopus 로고    scopus 로고
    • Insect growth regulatory effects of some extracts and sterols from Myrtillocactus geometrizans (Cactaceae) against Spodoptera frugiperda and Tenebrio molitor
    • Céspedes C.L., Salazar J.R., Martínez M., and Aranda E. Insect growth regulatory effects of some extracts and sterols from Myrtillocactus geometrizans (Cactaceae) against Spodoptera frugiperda and Tenebrio molitor. Phytochemistry 66 (2005) 2481-2493
    • (2005) Phytochemistry , vol.66 , pp. 2481-2493
    • Céspedes, C.L.1    Salazar, J.R.2    Martínez, M.3    Aranda, E.4
  • 9
    • 0031793484 scopus 로고    scopus 로고
    • Brassinosteroids: essential regulators of plant growth and development
    • Clouse S.D., and Sasse J.M. Brassinosteroids: essential regulators of plant growth and development. Annu. Rev. Plant Physiol. Plant Mol. Biol. 49 (1998) 427-451
    • (1998) Annu. Rev. Plant Physiol. Plant Mol. Biol. , vol.49 , pp. 427-451
    • Clouse, S.D.1    Sasse, J.M.2
  • 10
    • 0036743364 scopus 로고    scopus 로고
    • Arabidopsis mutants reveal multiple roles for sterols in plant development
    • Clouse S.D. Arabidopsis mutants reveal multiple roles for sterols in plant development. Plant Cell 14 (2002) 1995-2000
    • (2002) Plant Cell , vol.14 , pp. 1995-2000
    • Clouse, S.D.1
  • 11
    • 2942655136 scopus 로고    scopus 로고
    • Optimization of allylic oxidation of (1S, 3R, 8R)-2,2-dichloro-3,7,7,10-tetramethyltricyclo[6,4,01,3]dodec-9-ene
    • Dakir M., Auhmani A., Ait Itto My.Y., Mazoir N., Akssira M., Pierrot M., and Benharref A. Optimization of allylic oxidation of (1S, 3R, 8R)-2,2-dichloro-3,7,7,10-tetramethyltricyclo[6,4,01,3]dodec-9-ene. Synt. Commun. 34 (2004) 2001-2008
    • (2004) Synt. Commun. , vol.34 , pp. 2001-2008
    • Dakir, M.1    Auhmani, A.2    Ait Itto, My.Y.3    Mazoir, N.4    Akssira, M.5    Pierrot, M.6    Benharref, A.7
  • 13
    • 34249016432 scopus 로고    scopus 로고
    • Isolation of new phenylacetylingol derivatives that reactivate HIV-1 latency and a novel spirotriterpenoid from Euphorbia officinarum latex
    • Daoubi M., Marquez N., Mazoir N., Benharref A., Galán R.H., Muñoz E., and Collado I.G. Isolation of new phenylacetylingol derivatives that reactivate HIV-1 latency and a novel spirotriterpenoid from Euphorbia officinarum latex. Bioorg. Med. Chem. 15 (2007) 4577-4584
    • (2007) Bioorg. Med. Chem. , vol.15 , pp. 4577-4584
    • Daoubi, M.1    Marquez, N.2    Mazoir, N.3    Benharref, A.4    Galán, R.H.5    Muñoz, E.6    Collado, I.G.7
  • 17
    • 0030879001 scopus 로고    scopus 로고
    • Behavioral, sub-lethal effects of structurally-related lower terpenes on Myzus persicae
    • Gutierrez C., Fereres A., Reina M., Cabrera R., and Gonzalez-Coloma A. Behavioral, sub-lethal effects of structurally-related lower terpenes on Myzus persicae. J. Chem. Ecol. 23 (1997) 1641-1650
    • (1997) J. Chem. Ecol. , vol.23 , pp. 1641-1650
    • Gutierrez, C.1    Fereres, A.2    Reina, M.3    Cabrera, R.4    Gonzalez-Coloma, A.5
  • 18
    • 0032080517 scopus 로고    scopus 로고
    • Plant sterols and the membrane environment
    • Hartmann M.A. Plant sterols and the membrane environment. Trends Plant Sci. 3 (1998) 170-175
    • (1998) Trends Plant Sci. , vol.3 , pp. 170-175
    • Hartmann, M.A.1
  • 20
    • 0016761975 scopus 로고
    • Resiniferatoxin and other esters of novel polyfunctional diterpenes from Euphorbia resinifera and unispina
    • Hergenhahn M., Adolph W., and Hecker E. Resiniferatoxin and other esters of novel polyfunctional diterpenes from Euphorbia resinifera and unispina. Tetrahedron Lett. 16 (1975) 1595-1598
    • (1975) Tetrahedron Lett. , vol.16 , pp. 1595-1598
    • Hergenhahn, M.1    Adolph, W.2    Hecker, E.3
  • 21
    • 1442278154 scopus 로고    scopus 로고
    • Morphological and molecular effects of 20-hydroxyecdysone and its agonist tebufenozide on CF-203, a midgut-derived cell line from the spruce budworm, Choristoneura fumiferana
    • Hu W., Cook B.J., Ampasala D.R., Zheng S., Caputo G., Krell P.J., Retnakaran A., Arif B.M., and Feng Q. Morphological and molecular effects of 20-hydroxyecdysone and its agonist tebufenozide on CF-203, a midgut-derived cell line from the spruce budworm, Choristoneura fumiferana. Arch. Insect Biochem. Physiol. 55 (2004) 68-78
    • (2004) Arch. Insect Biochem. Physiol. , vol.55 , pp. 68-78
    • Hu, W.1    Cook, B.J.2    Ampasala, D.R.3    Zheng, S.4    Caputo, G.5    Krell, P.J.6    Retnakaran, A.7    Arif, B.M.8    Feng, Q.9
  • 22
    • 18844383202 scopus 로고    scopus 로고
    • Ganoderic acid X, a lanostanoid triterpene, inhibits topoisomerases and induces apoptosis of cancer cells
    • Li C.H., Chen P.Y., Chang U.M., Kan L.S., Fang W.H., Tsai K.S., and Lin S.B. Ganoderic acid X, a lanostanoid triterpene, inhibits topoisomerases and induces apoptosis of cancer cells. Life Sci. 77 (2005) 252-265
    • (2005) Life Sci. , vol.77 , pp. 252-265
    • Li, C.H.1    Chen, P.Y.2    Chang, U.M.3    Kan, L.S.4    Fang, W.H.5    Tsai, K.S.6    Lin, S.B.7
  • 24
    • 33646371229 scopus 로고    scopus 로고
    • Within-species variability of the response to 20 hydroxyecdysone in peach - potato aphid (Myzus persicae Sulzer)
    • Malausa T., Salles M., Marquet V., Guillemaud T., Alla S., Marion-Poll F., and Lapchin L. Within-species variability of the response to 20 hydroxyecdysone in peach - potato aphid (Myzus persicae Sulzer). J. Insect Physiol. 52 (2006) 480-486
    • (2006) J. Insect Physiol. , vol.52 , pp. 480-486
    • Malausa, T.1    Salles, M.2    Marquet, V.3    Guillemaud, T.4    Alla, S.5    Marion-Poll, F.6    Lapchin, L.7
  • 25
    • 0344820768 scopus 로고    scopus 로고
    • Lipid composition of Spodoptera frugiperda (Sf9) and Trichoplusia ni (Tn) insect cells used for baculovirus infection
    • Marheineke K., Grunewald S., Christie W., and Reiländer H. Lipid composition of Spodoptera frugiperda (Sf9) and Trichoplusia ni (Tn) insect cells used for baculovirus infection. FEBS Lett. 441 (1998) 49-52
    • (1998) FEBS Lett. , vol.441 , pp. 49-52
    • Marheineke, K.1    Grunewald, S.2    Christie, W.3    Reiländer, H.4
  • 26
    • 0036268898 scopus 로고    scopus 로고
    • Taste detection of phytoecdysteroids in larvae of Bombyx mori, Spodoptera littoralis and Ostrinia nubilalis
    • Marion-Poll F., and Descoins C. Taste detection of phytoecdysteroids in larvae of Bombyx mori, Spodoptera littoralis and Ostrinia nubilalis. J. Insect Physiol. 48 (2002) 467-476
    • (2002) J. Insect Physiol. , vol.48 , pp. 467-476
    • Marion-Poll, F.1    Descoins, C.2
  • 27
    • 41049096788 scopus 로고    scopus 로고
    • Mazoir, N., Auhmani, A., Ait Itto, M.Y., Benharref, A., 2004a. (3 S)-Acetyl-24-methyl-elemo-lanosta-8,24(31)-diene-7,11-dione. Molbank, M365 (MOL File: m365.mol).
    • Mazoir, N., Auhmani, A., Ait Itto, M.Y., Benharref, A., 2004a. (3 S)-Acetyl-24-methyl-elemo-lanosta-8,24(31)-diene-7,11-dione. Molbank, M365 (MOL File: m365.mol).
  • 28
    • 41049100312 scopus 로고    scopus 로고
    • Mazoir, N., Auhmani, A., Dakir, M., Ait Itto, M.Y., Benharref, A., 2004b. (3 S)-Tosyl-24-methyl-elemo-lanosta-8,24(31)-diene-7,11-dione. Molbank, M366 (MOL File: m366.mol).
    • Mazoir, N., Auhmani, A., Dakir, M., Ait Itto, M.Y., Benharref, A., 2004b. (3 S)-Tosyl-24-methyl-elemo-lanosta-8,24(31)-diene-7,11-dione. Molbank, M366 (MOL File: m366.mol).
  • 31
    • 41049099381 scopus 로고    scopus 로고
    • Mazoir, N., Daoubi, M., Lassaba, E., Benharref, A., 2006. 3β-Acetoxy-elemo-lanost-8-en-24-one. Molbank, M506 (MOL File: m506.mol).
    • Mazoir, N., Daoubi, M., Lassaba, E., Benharref, A., 2006. 3β-Acetoxy-elemo-lanost-8-en-24-one. Molbank, M506 (MOL File: m506.mol).
  • 32
    • 13044264415 scopus 로고    scopus 로고
    • The phytogeographical significance of S.W. Morocco compared to the Canary Islands
    • Médail F., and Quézel P. The phytogeographical significance of S.W. Morocco compared to the Canary Islands. Plant Ecol. 140 (1999) 221-244
    • (1999) Plant Ecol. , vol.140 , pp. 221-244
    • Médail, F.1    Quézel, P.2
  • 34
    • 45849103593 scopus 로고    scopus 로고
    • Moreno-Osorio, L., Cortes, M., Armstrong, V., Bailén, M., González-Coloma, A., 2008. Antifeedant activity of some polygodial derivatives. Z. Naturforsch. C, in press.
    • Moreno-Osorio, L., Cortes, M., Armstrong, V., Bailén, M., González-Coloma, A., 2008. Antifeedant activity of some polygodial derivatives. Z. Naturforsch. C, in press.
  • 35
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays
    • Mossman T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Meth. 65 (1983) 55-63
    • (1983) J. Immunol. Meth. , vol.65 , pp. 55-63
    • Mossman, T.1
  • 36
    • 33644642843 scopus 로고    scopus 로고
    • Lipid signaling in plants. Cloning and expression analysis of the obtusifoliol 14(-demethylase from Solanum chacoense Bitt., a pollination- and fertilization-induced gene with both obtusifoliol and lanosterol demethylase activity
    • O'Brien M., Chantha S.C., Rahier A., and Matton D.P. Lipid signaling in plants. Cloning and expression analysis of the obtusifoliol 14(-demethylase from Solanum chacoense Bitt., a pollination- and fertilization-induced gene with both obtusifoliol and lanosterol demethylase activity. Plant Physiol. 139 (2005) 734-749
    • (2005) Plant Physiol. , vol.139 , pp. 734-749
    • O'Brien, M.1    Chantha, S.C.2    Rahier, A.3    Matton, D.P.4
  • 37
    • 30744439833 scopus 로고    scopus 로고
    • Absolute configuration and conformational disorder of a tricyclic thiosemicarbazone derivative
    • Ourhriss N., Giorgi M., Mazoir N., and Benharref A. Absolute configuration and conformational disorder of a tricyclic thiosemicarbazone derivative. Acta Crystallogr. C61 (2005) 699-701
    • (2005) Acta Crystallogr. , vol.C61 , pp. 699-701
    • Ourhriss, N.1    Giorgi, M.2    Mazoir, N.3    Benharref, A.4
  • 38
    • 0030843180 scopus 로고    scopus 로고
    • Fungicides as tools in studying postsqualene sterol synthesis in plants
    • Rahier A., and Taton M. Fungicides as tools in studying postsqualene sterol synthesis in plants. Pestic. Biochem. Physiol. 57 (1997) 1-27
    • (1997) Pestic. Biochem. Physiol. , vol.57 , pp. 1-27
    • Rahier, A.1    Taton, M.2
  • 40
    • 0037402336 scopus 로고    scopus 로고
    • The role of sterols in plant growth and development
    • Schaller H. The role of sterols in plant growth and development. Prog. Lipid Res. 42 (2003) 163-175
    • (2003) Prog. Lipid Res. , vol.42 , pp. 163-175
    • Schaller, H.1
  • 41
    • 0036236048 scopus 로고    scopus 로고
    • Inhibition of tumor-promoting effects by poricoric acids H and H and other lanostane-type triterpenes and cytotoxic activity of poricoric acids A and G from Poria cocos
    • Ukiya M., Akihisa T., Tokuda H., Hirano M., Oshikubo M., Nobukuni Y., Kimura Y., Tai T., Kondo S., and Nishino H. Inhibition of tumor-promoting effects by poricoric acids H and H and other lanostane-type triterpenes and cytotoxic activity of poricoric acids A and G from Poria cocos. J. Nat. Prod. 65 (2002) 462-465
    • (2002) J. Nat. Prod. , vol.65 , pp. 462-465
    • Ukiya, M.1    Akihisa, T.2    Tokuda, H.3    Hirano, M.4    Oshikubo, M.5    Nobukuni, Y.6    Kimura, Y.7    Tai, T.8    Kondo, S.9    Nishino, H.10
  • 42
    • 0038188709 scopus 로고    scopus 로고
    • Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus
    • Wang L.Y., Wang N.L., Yao X.S., Miyata S., and Kitanaka S. Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus. J. Nat. Prod. 66 (2003) 630-633
    • (2003) J. Nat. Prod. , vol.66 , pp. 630-633
    • Wang, L.Y.1    Wang, N.L.2    Yao, X.S.3    Miyata, S.4    Kitanaka, S.5
  • 43
    • 0029620632 scopus 로고
    • Enzymes of ecdysteroid transformation and inactivation in the midgut of the cotton leafworm Spodoptera littoralis: properties and development profiles
    • Webb T.J., Fowls R., and Rees H.H. Enzymes of ecdysteroid transformation and inactivation in the midgut of the cotton leafworm Spodoptera littoralis: properties and development profiles. Biochem. J. 312 (1995) 561-568
    • (1995) Biochem. J. , vol.312 , pp. 561-568
    • Webb, T.J.1    Fowls, R.2    Rees, H.H.3
  • 44
    • 0034085563 scopus 로고    scopus 로고
    • Inhibitory effects of euphol, a triterpene alcohol from the roots of Euphorbia kansui, on tumour promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skin
    • Yasukawa K., Akihisa T., Yoshida Z.Y., and Takido M. Inhibitory effects of euphol, a triterpene alcohol from the roots of Euphorbia kansui, on tumour promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skin. J. Pharm. Pharmacol. 52 (2000) 119-124
    • (2000) J. Pharm. Pharmacol. , vol.52 , pp. 119-124
    • Yasukawa, K.1    Akihisa, T.2    Yoshida, Z.Y.3    Takido, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.