메뉴 건너뛰기




Volumn 72, Issue 14-15, 2011, Pages 1804-1813

Triterpenes and neolignans from the roots of Nannoglottis carpesioides

Author keywords

Antioxidant; Asteraceae; Cytotoxic; Nannoglottis carpesioides; Neolignans; Triterpenes

Indexed keywords

ANTINEOPLASTIC AGENT; ANTIOXIDANT; LIGNAN; PLANT EXTRACT; TRITERPENE;

EID: 80051552980     PISSN: 00319422     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytochem.2011.05.008     Document Type: Article
Times cited : (21)

References (39)
  • 2
    • 18544376110 scopus 로고    scopus 로고
    • 17β-Hydroxy-28-norolean-12-ene-3, 16-dione
    • S.-P. Bai, and L. Yang 17β-Hydroxy-28-norolean-12-ene-3, 16-dione Acta Cryst. E61 2005 o967 o968
    • (2005) Acta Cryst. , vol.61 E
    • Bai, S.-P.1    Yang, L.2
  • 3
    • 84989405912 scopus 로고
    • Sesquiterpenes with new carbon skeletons, furceremophilanes, secoeremcphilanes and other constituents from Argentinian senecio species
    • F. Bohlmann, J. Jakupovic, U. Warning, M. Grenz, T.V. Chau-Thi, R.M. King, and H. Robinson Sesquiterpenes with new carbon skeletons, furceremophilanes, secoeremcphilanes and other constituents from Argentinian senecio species Bull. Soc. Chim. Bolg. 95 1986 707 736
    • (1986) Bull. Soc. Chim. Bolg. , vol.95 , pp. 707-736
    • Bohlmann, F.1    Jakupovic, J.2    Warning, U.3    Grenz, M.4    Chau-Thi, T.V.5    King, R.M.6    Robinson, H.7
  • 5
    • 66449100339 scopus 로고    scopus 로고
    • The assignment of absolute stereostructures through quantum chemical circular dichroism calculations
    • G. Bringmann, T. Bruhn, K. Maksimenka, and Y. Hemberger The assignment of absolute stereostructures through quantum chemical circular dichroism calculations Eur. J. Org. Chem. 2009 2009 2717 2727
    • (2009) Eur. J. Org. Chem. , vol.2009 , pp. 2717-2727
    • Bringmann, G.1    Bruhn, T.2    Maksimenka, K.3    Hemberger, Y.4
  • 6
    • 43949163247 scopus 로고
    • Terpenoid glycosides from the roots of Aster tataricus
    • DOI 10.1016/S0031-9422(00)90528-4
    • D.-L. Cheng, and Y. Shao Terpenoid glycosides from the roots of Aster tataricus Phytochemistry 35 1994 173 176 (Pubitemid 2032267)
    • (1994) Phytochemistry , vol.35 , Issue.1 , pp. 173-176
    • Cheng, D.1    Shao, Y.2
  • 7
    • 0037431283 scopus 로고    scopus 로고
    • Systematic investigation of modern quantum chemical methods to predict electronic circular dichroism spectra
    • C. Diedrich, and S. Grimme Systematic investigation of modern quantum chemical methods to predict electronic circular dichroism spectra J. Phys. Chem. A 107 2003 2524 2539
    • (2003) J. Phys. Chem. A , vol.107 , pp. 2524-2539
    • Diedrich, C.1    Grimme, S.2
  • 8
    • 0033386450 scopus 로고    scopus 로고
    • Diterpenes from Haplopappus chrysanthemifolius
    • DOI 10.1016/S0031-9422(99)00395-7, PII S0031942299003957
    • F. Faini, C. Labbé, R. Torres, F. Delle Monache, and G. Delle Monache Diterpenes from Haplopappus chrysanthemifolius Phytochemistry 52 1999 1547 1550 (Pubitemid 30019604)
    • (1999) Phytochemistry , vol.52 , Issue.8 , pp. 1547-1550
    • Faini, F.1    Labbe, C.2    Torres, R.3    Delle Monache, F.4    Delle Monache, G.5
  • 11
    • 21744459616 scopus 로고    scopus 로고
    • Microcharacters in the ligules of Nannoglottis (Compositae) and their systematic significance
    • DOI 10.1360/aps030077
    • T.-G. Gao, and Y.-L. Chen Microcharacters in the ligules of Nannoglottis (Compositae) and their systematic significance Acta Phytotax. Sin. 43 2005 12 21 (Pubitemid 40938681)
    • (2005) Acta Phytotaxonomica Sinica , vol.43 , Issue.1 , pp. 12-21
    • Gao, T.-G.1    Chen, Y.-L.2
  • 13
    • 0027531682 scopus 로고
    • A new approach for measurement of cytotoxicity using colorimetric assay
    • R.F. Hussain, A.M.E. Nouri, and R.T.D. Oliver A new approach for measurement of cytotoxicity using colorimetric assay J. Immunol. Methods 160 1993 89 96
    • (1993) J. Immunol. Methods , vol.160 , pp. 89-96
    • Hussain, R.F.1    Nouri, A.M.E.2    Oliver, R.T.D.3
  • 14
    • 0029152546 scopus 로고
    • Triterpenoids from callus tissue cultures of Paeonia species
    • A. Ikuta, K. Kamiya, T. Satake, and Y. Saiki Triterpenoids from callus tissue cultures of Paeonia species Phytochemistry 38 1995 1203 1207
    • (1995) Phytochemistry , vol.38 , pp. 1203-1207
    • Ikuta, A.1    Kamiya, K.2    Satake, T.3    Saiki, Y.4
  • 15
    • 0002766084 scopus 로고
    • Two triterpenes from the flowers of Camellia japonica
    • H. Itokawa, H. Nakajima, A. Ikuta, and Y. Litaka Two triterpenes from the flowers of Camellia japonica Phytochemistry 20 1981 2539 2542
    • (1981) Phytochemistry , vol.20 , pp. 2539-2542
    • Itokawa, H.1    Nakajima, H.2    Ikuta, A.3    Litaka, Y.4
  • 16
    • 72449136816 scopus 로고    scopus 로고
    • A new dicaffeoyl quinic acid from Nannoglottis ravida
    • J. Jiang, B.-B. Zhang, and Z.-X. Liao A new dicaffeoyl quinic acid from Nannoglottis ravida Chin. Chem. Lett. 21 2010 203 205
    • (2010) Chin. Chem. Lett. , vol.21 , pp. 203-205
    • Jiang, J.1    Zhang, B.-B.2    Liao, Z.-X.3
  • 17
    • 0031699663 scopus 로고    scopus 로고
    • Revised structure for a neolignan from Brucea javanica
    • DOI 10.1016/S0031-9422(98)00449-X, PII S003194229800449X
    • S.-M. Li, K. Lundquist, and A.F.A. Wallis Revised structure for a neolignan from Brucea javanica Phytochemistry 49 1998 2125 2128 (Pubitemid 28563833)
    • (1998) Phytochemistry , vol.49 , Issue.7 , pp. 2125-2128
    • Li, S.1    Lundquist, K.2    Wallis, A.F.A.3
  • 18
    • 31344434165 scopus 로고    scopus 로고
    • Lignans from Wikstroemia hainanensis
    • DOI 10.1002/hlca.200690014
    • S.-G. Liao, Y. Wu, and J.-M. Yue Lignans from Wikstroemia hainanensis Helv. Chim. Acta 89 2006 73 80 (Pubitemid 43145535)
    • (2006) Helvetica Chimica Acta , vol.89 , Issue.1 , pp. 73-80
    • Liao, S.-G.1    Wu, Y.2    Yue, J.-M.3
  • 19
    • 0009755198 scopus 로고    scopus 로고
    • Floral microcharacters of the subtribe Tussilagininae (Asteraceae: Senecioneae) of the eastern Asia and their systematic and taxonomic significance
    • J.-Q. Liu Floral microcharacters of the subtribe Tussilagininae (Asteraceae: Senecioneae) of the eastern Asia and their systematic and taxonomic significance Bull. Bot. Res. 21 2001 11 27
    • (2001) Bull. Bot. Res. , vol.21 , pp. 11-27
    • Liu, J.-Q.1
  • 20
    • 0009775341 scopus 로고    scopus 로고
    • Systematic position of Nannoglottis Maxim. s.l. (Asteraceae): Karyomorphological data
    • J.-Q. Liu, T.-N. Ho, and S.-W. Liu Systematic position of Nannoglottis Maxim. s.l. (Asteraceae): karyomorphological data Acta Phytotaxon. Sin. 38 2000 236 241
    • (2000) Acta Phytotaxon. Sin. , vol.38 , pp. 236-241
    • Liu, J.-Q.1    Ho, T.-N.2    Liu, S.-W.3
  • 22
    • 0029842315 scopus 로고    scopus 로고
    • Studies on the constituents of Lonicera species. X. Neolignan glycosides from the leaves of Lonicera gracilipes var. glandulosa MAXIM
    • N. Matsuda, and M. Kikuchi Studies on the constituents of Lonicera species. X. neolignan glycosides from the leaves of Lonicera gracilipes var. glandulosa Maxim Chem. Pharm. Bull. 44 1996 1676 1679 (Pubitemid 26342281)
    • (1996) Chemical and Pharmaceutical Bulletin , vol.44 , Issue.9 , pp. 1676-1679
    • Matsuda, N.1    Kikuchi, M.2
  • 23
    • 85008131223 scopus 로고
    • Studies on the constituents of Aster tataricus L.f. II. structures of Aster saponins isolated from the root
    • T. Nagao, S. Hachiyama, H. Okabe, and T. Yamauchi Studies on the constituents of Aster tataricus L.f. II. structures of Aster saponins isolated from the root Chem. Pharm. Bull. 37 1989 1977 1983
    • (1989) Chem. Pharm. Bull. , vol.37 , pp. 1977-1983
    • Nagao, T.1    Hachiyama, S.2    Okabe, H.3    Yamauchi, T.4
  • 24
    • 4644336696 scopus 로고    scopus 로고
    • Clerodane-type diterpenoids from Nannoglottis ravida
    • DOI 10.1016/j.phytochem.2004.08.015, PII S0031942204003917, Reports on Structure Elucidation
    • H.-L. Qin, and Z.-H. Li Clerodane-type diterpenoids from Nannoglottis ravida Phytochemistry 65 2004 2533 2537 (Pubitemid 39286612)
    • (2004) Phytochemistry , vol.65 , Issue.18 , pp. 2533-2537
    • Qin, H.-L.1    Li, Z.-H.2
  • 25
    • 0032982508 scopus 로고    scopus 로고
    • Antioxidant activity applying an improved ABTS radical cation decolorization assay
    • DOI 10.1016/S0891-5849(98)00315-3, PII S0891584998003153
    • R. Re, N. Pellegrini, A. Proteggente, A. Pannala, M. Yang, and C. Rice-Evans Antioxidant activity applying an improved ABTS radical cation decolorization assay Free Radical Biol. Med. 26 1999 1231 1237 (Pubitemid 29262709)
    • (1999) Free Radical Biology and Medicine , vol.26 , Issue.9-10 , pp. 1231-1237
    • Re, R.1    Pellegrini, N.2    Proteggente, A.3    Pannala, A.4    Yang, M.5    Rice-Evans, C.6
  • 26
    • 0000277612 scopus 로고
    • Noroleanane saponins from Celmisia petriei
    • D.D. Rowan, and R.H. Newman Noroleanane saponins from Celmisia petriei Phytochemistry 23 1984 639 644
    • (1984) Phytochemistry , vol.23 , pp. 639-644
    • Rowan, D.D.1    Newman, R.H.2
  • 28
    • 0037364960 scopus 로고    scopus 로고
    • New dihydrobenzofurans and triterpenoids from roots of Microglossa pyrifolia
    • DOI 10.1055/s-2003-38480
    • T.J. Schmidt, M.R. Hildebrand, and G. Willuhn New dihydrobenzofurans and triterpenoids from roots of Microglossa pyrifolia Planta Med. 69 2003 258 264 (Pubitemid 36470132)
    • (2003) Planta Medica , vol.69 , Issue.3 , pp. 258-264
    • Schmidt, T.J.1    Hildebrand, M.R.2    Willuhn, G.3
  • 29
    • 77956340774 scopus 로고    scopus 로고
    • Dibenzocyclooctadiene lignans from Magnolia and Talauma (Magnoliaceae): Their absolute configuration ascertained by circular dichroism and X-ray crystallography and re-evaluation of previously published pyramidatin structures
    • W. Schühly, B. Grölacher, J. Neyer, W.M.F. Fabian, F.R. Fronczek, and O. Kunert Dibenzocyclooctadiene lignans from Magnolia and Talauma (Magnoliaceae): Their absolute configuration ascertained by circular dichroism and X-ray crystallography and re-evaluation of previously published pyramidatin structures Phytochemistry 71 2010 1787 1795
    • (2010) Phytochemistry , vol.71 , pp. 1787-1795
    • Schühly, W.1    Grölacher, B.2    Neyer, J.3    Fabian, W.M.F.4    Fronczek, F.R.5    Kunert, O.6
  • 32
    • 0033609779 scopus 로고    scopus 로고
    • Piceanonols A, and B, triterpenoids bearing a novel skeletal system isolated from the bark of Picea jezoensis var. hondoensis
    • DOI 10.1016/S0040-4039(99)01190-9, PII S0040403999011909
    • R. Tanaka, T. Kumagai, Y. In, T. Ishida, H. Nishino, and S. Matsunaga Piceanonols A, and B, triterpenoids bearing a novel skeletal system isolated from the bark of Picea jezoensis var. hondoensis Tetrahedron Lett. 40 1999 6415 6418 (Pubitemid 29389876)
    • (1999) Tetrahedron Letters , vol.40 , Issue.35 , pp. 6415-6418
    • Tanaka, R.1    Kumagai, T.2    In, Y.3    Ishida, T.4    Nishino, H.5    Matsunaga, S.6
  • 33
    • 13844276772 scopus 로고    scopus 로고
    • Clerodane diterpenoids from Microglossa angolensis
    • DOI 10.1016/j.tet.2005.01.051
    • M. Tene, P. Tane, B.L. Sondengam, and J.D. Connolly Clerodane diterpenoids from Microglossa angolensis Tetrahedron 61 2005 2655 2658 (Pubitemid 40255231)
    • (2005) Tetrahedron , vol.61 , Issue.10 , pp. 2655-2658
    • Tene, M.1    Tane, P.2    Sondengam, B.L.3    Connolly, J.D.4
  • 34
    • 78449269782 scopus 로고    scopus 로고
    • 28-Nor-oleanane-type triterpene saponins from Camellia japonica and their inhibitory activity on LPS-induced NO production in macrophage RAW264.7 cells
    • N.T.P. Thao, T.M. Hung, T.D. Cuong, J.C. Kim, E.H. Kim, S.E. Jin, M.K. Na, Y.M. Lee, Y.H. Kim, J.S. Choi, and B.S. Min 28-Nor-oleanane-type triterpene saponins from Camellia japonica and their inhibitory activity on LPS-induced NO production in macrophage RAW264.7 cells Bioorg. Med. Chem. Lett. 20 2010 7435 7439
    • (2010) Bioorg. Med. Chem. Lett. , vol.20 , pp. 7435-7439
    • Thao, N.T.P.1    Hung, T.M.2    Cuong, T.D.3    Kim, J.C.4    Kim, E.H.5    Jin, S.E.6    Na, M.K.7    Lee, Y.M.8    Kim, Y.H.9    Choi, J.S.10    Min, B.S.11
  • 35
    • 0025730943 scopus 로고
    • 24, 28-Dinor-18α-oleanane, a novel demethylated higher plant derived triterpene hydrocarbon in petroleum
    • J.M. Trendel, R. Graft, P. Albrecht, and A. Riva 24, 28-Dinor-18α- oleanane, a novel demethylated higher plant derived triterpene hydrocarbon in petroleum Tetrahedron Lett. 32 1991 2959 2962
    • (1991) Tetrahedron Lett. , vol.32 , pp. 2959-2962
    • Trendel, J.M.1    Graft, R.2    Albrecht, P.3    Riva, A.4
  • 36
    • 33846219958 scopus 로고    scopus 로고
    • Saponins, classification and occurrence in the plant kingdom
    • DOI 10.1016/j.phytochem.2006.10.008, PII S0031942206006480
    • J.-P. Vincken, L. Heng, A. de Groot, and H. Gruppen Saponins, classification and occurrence in the plant kingdom Phytochemistry 68 2007 275 297 (Pubitemid 46108037)
    • (2007) Phytochemistry , vol.68 , Issue.3 , pp. 275-297
    • Vincken, J.-P.1    Heng, L.2    De Groot, A.3    Gruppen, H.4
  • 37
    • 33745766635 scopus 로고    scopus 로고
    • Triterpenoids from the resin of Styrax tonkinensis and their antiproliferative and differentiation effects in human leukemia HL-60 cells
    • DOI 10.1021/np050371z
    • F. Wang, H.-M. Hua, Y.-H. Pei, D. Chen, and Y.-K. Jing Triterpenoids from the resin of Styrax tonkinensis and their antiproliferative and differentiation effects in Human Leukemia HL-60 Cells J. Nat. Prod. 69 2006 807 810 (Pubitemid 44021410)
    • (2006) Journal of Natural Products , vol.69 , Issue.5 , pp. 807-810
    • Wang, F.1    Hua, H.2    Pei, Y.3    Chen, D.4    Jing, Y.5
  • 38
    • 34147130105 scopus 로고    scopus 로고
    • Medicinal flowers. XV. The structures of noroleanane- and oleanane-type triterpene oligoglycosides with gastroprotective and platelet aggregation activities from flower buds of Camellia japonica
    • DOI 10.1248/cpb.55.606
    • M. Yoshikawa, T. Morikawa, Y. Asao, E. Fujiwara, S. Nakamura, and H. Matsuda Medicinal flowers. XV.1 the structures of noroleanane- and oleanane-type triterpene oligoglycosides with gastroprotective and platelet aggregation activities from flower buds of Camellia japonica Chem. Pharm. Bull. 55 2007 606 612 (Pubitemid 46570841)
    • (2007) Chemical and Pharmaceutical Bulletin , vol.55 , Issue.4 , pp. 606-612
    • Yoshikawa, M.1    Morikawa, T.2    Asao, Y.3    Fujiwara, E.4    Nakamura, S.5    Matsuda, H.6
  • 39
    • 0035439092 scopus 로고    scopus 로고
    • New noroleanane-type triterpene saponins with gastroprotective effect and platelet aggregation activity from the flowers of Camellia japonica: Revised structures of camellenodiol and camelledionol
    • M. Yoshikawa, T. Morikawa, E. Fujiwara, T. Ohgushi, Y. Asao, and H. Matsuda New noroleanane-type triterpene saponins with gastroprotective effect and platelet aggregation activity from the flowers of Camellia japonica: revised structures of camellenodiol and camelledionol Heterocycles 55 2001 1653 1658
    • (2001) Heterocycles , vol.55 , pp. 1653-1658
    • Yoshikawa, M.1    Morikawa, T.2    Fujiwara, E.3    Ohgushi, T.4    Asao, Y.5    Matsuda, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.