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Volumn 69, Issue 9, 2003, Pages 846-850

Terpenoids of Salvia hydrangea: Two New, Rearranged 20-Norabietanes and the Effect of Oleanolic Acid on Erythrocyte Membranes

Author keywords

Erythrocyte membrane; Lamiaceae; Norabietanes; Plasmodium falciparum; Royleanones; Salvia hydrangea; Stomatocytes

Indexed keywords

20 NORABIETANE DERIVATIVE; ANTHELMINTIC AGENT; ANTILEISHMANIAL AGENT; CHLOROQUINE; HERBACEOUS AGENT; NORMULTICAULINE; OLEANOLIC ACID; PLANT EXTRACT; ROYLEANONE DERIVATIVE; SALVIA HYDRANGEA EXTRACT; TERPENOID DERIVATIVE; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0242351906     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-43212     Document Type: Article
Times cited : (36)

References (25)
  • 7
    • 0030770277 scopus 로고    scopus 로고
    • Abietane and icetexane diterpenoids from Salvia ballotaeflora and Salvia axillaris
    • Esquivel B, Calderon JS, Flores E, Sanchez AA, Rivera RR. Abietane and icetexane diterpenoids from Salvia ballotaeflora and Salvia axillaris. Phytochemistry 1997; 46: 531-4
    • (1997) Phytochemistry , vol.46 , pp. 531-534
    • Esquivel, B.1    Calderon, J.S.2    Flores, E.3    Sanchez, A.A.4    Rivera, R.R.5
  • 8
    • 0343776172 scopus 로고    scopus 로고
    • Diterpenoids from Salvia glutinosa, S. austriaca, S. tomentosa and S. verticillata roots
    • Nagy G, Günther G, Mathe I, Blunden G, Yang M, Crabb TA. Diterpenoids from Salvia glutinosa, S. austriaca, S. tomentosa and S. verticillata roots. Phytochemistry 1999; 52: 1105-9
    • (1999) Phytochemistry , vol.52 , pp. 1105-1109
    • Nagy, G.1    Günther, G.2    Mathe, I.3    Blunden, G.4    Yang, M.5    Crabb, T.A.6
  • 9
    • 0016163747 scopus 로고
    • Das Vorkommen von Phenanthrenchinonen in Arten der Gattung Salvia
    • Patudin A, Romanowa A, Sokolow WS, Pribylowa G. Das Vorkommen von Phenanthrenchinonen in Arten der Gattung Salvia. Planta Medica 1974; 26: 201-7
    • (1974) Planta Medica , vol.26 , pp. 201-207
    • Patudin, A.1    Romanowa, A.2    Sokolow, W.S.3    Pribylowa, G.4
  • 10
    • 0007071574 scopus 로고
    • Teheran: Ministry of Health Publications
    • Amin G. Popular Medicinal Plants of Iran; Vol 1., Teheran: Ministry of Health Publications, 1991: 41
    • (1991) Popular Medicinal Plants of Iran , vol.1 , pp. 41
    • Amin, G.1
  • 15
    • 0242320574 scopus 로고
    • The total synthesis of (+)-taxoqionone, (-)-7α-acetoxyroyleanone, (-)-dehydroroyleanone, (-)-horminone, (-)-7-oxoroyleanone, and (+)-inurpyleanol
    • Matsumoto T, Hasrada S. The total synthesis of (+)-taxoqionone, (-)-7α-acetoxyroyleanone, (-)-dehydroroyleanone, (-)-horminone, (-)-7-oxoroyleanone, and (+)-inurpyleanol. Bulletin of the Chemical Society of Japan 1979; 52: 1459-63
    • (1979) Bulletin of the Chemical Society of Japan , vol.52 , pp. 1459-1463
    • Matsumoto, T.1    Hasrada, S.2
  • 16
    • 0036237883 scopus 로고    scopus 로고
    • In vitro Plasmodium falciparum drug sensitivity assay: Inhibition of parasite growth by incorporation of stomatocytogenic amphiphiles into erythrocyte membrane
    • Ziegler HL, Stærk D, Christensen J, Hviid L, Hägerstrand H, Jaroszewski JW. In vitro Plasmodium falciparum drug sensitivity assay: inhibition of parasite growth by incorporation of stomatocytogenic amphiphiles into erythrocyte membrane. Antimicrobial Agents and Chemotherapy 2002; 46: 1441-6
    • (2002) Antimicrobial Agents and Chemotherapy , vol.46 , pp. 1441-1446
    • Ziegler, H.L.1    Stærk, D.2    Christensen, J.3    Hviid, L.4    Hägerstrand, H.5    Jaroszewski, J.W.6
  • 17
    • 0036067277 scopus 로고    scopus 로고
    • Possible artefacts in the in vitro determination of antimalarial activity of natural products that incorporate into lipid bilayer: Apparent antiplasmodial activity of dehydroabietinol, a constituent of Hyptis suaveolens
    • Ziegler HL, Jensen TH, Christensen J, Stærk D, Hägerstrand H, Sittie AA, Olesen CE, Staalsø T, Ekpe P, Jaroszewski JW. Possible artefacts in the in vitro determination of antimalarial activity of natural products that incorporate into lipid bilayer: apparent antiplasmodial activity of dehydroabietinol, a constituent of Hyptis suaveolens. Planta Medica 2002; 68: 547-9
    • (2002) Planta Medica , vol.68 , pp. 547-549
    • Ziegler, H.L.1    Jensen, T.H.2    Christensen, J.3    Stærk, D.4    Hägerstrand, H.5    Sittie, A.A.6    Olesen, C.E.7    Staalsø, T.8    Ekpe, P.9    Jaroszewski, J.W.10
  • 18
    • 0002163969 scopus 로고
    • Red cell shapes, an illustrated classification and its rationale
    • Bessis M, Weed RI, Leblond PF (eds.). Heidelberg: Springer-Verlag
    • Bessis M. Red cell shapes, an illustrated classification and its rationale. In Bessis M, Weed RI, Leblond PF (eds.). Red Cell Shape. Physiology, Pathology, Ultrastructure. Heidelberg: Springer-Verlag, 1973: 1-24
    • (1973) Red Cell Shape. Physiology, Pathology, Ultrastructure , pp. 1-24
    • Bessis, M.1
  • 19
    • 0031442788 scopus 로고    scopus 로고
    • Norditerpenoids and diterpenoids from Salvia multicaulis with antituberculous activity
    • Ulubelen A, Topcu G, Johansson CB. Norditerpenoids and diterpenoids from Salvia multicaulis with antituberculous activity. Journal of Natural Products 1997; 60: 1275-80
    • (1997) Journal of Natural Products , vol.60 , pp. 1275-1280
    • Ulubelen, A.1    Topcu, G.2    Johansson, C.B.3
  • 20
    • 0242383066 scopus 로고
    • The photocycloaddition of methoxynaphthalenes with acetylenes and acid-catalysed retardation: Reactions of non-fluorescent exciplexes
    • Chow YL, Buono-Core GE, Zhang LM, Johansson CI. The photocycloaddition of methoxynaphthalenes with acetylenes and acid-catalysed retardation: reactions of non-fluorescent exciplexes. Journal of Chemical Society, Perkin Transactions 2 1995: 1691-8
    • (1995) Journal of Chemical Society, Perkin Transactions 2 , pp. 1691-1698
    • Chow, Y.L.1    Buono-Core, G.E.2    Zhang, L.M.3    Johansson, C.I.4
  • 21
    • 84986840493 scopus 로고
    • 13C Substituent effects on monosubstituted benzenes
    • 13C Substituent effects on monosubstituted benzenes. Organic Magnetic Resonance 1979; 12: 499-524
    • (1979) Organic Magnetic Resonance , vol.12 , pp. 499-524
    • Ewing, D.E.1
  • 22
    • 0242383068 scopus 로고
    • H-H, C-H and C-C NMR spin-spin coupling constants calculated by the FP-INDO method for aromatic hydrocarbons
    • Long SAT, Memory JD. H-H, C-H and C-C NMR spin-spin coupling constants calculated by the FP-INDO method for aromatic hydrocarbons. Journal of Magnetic Resonance 1978; 29: 119-24
    • (1978) Journal of Magnetic Resonance , vol.29 , pp. 119-124
    • Long, S.A.T.1    Memory, J.D.2
  • 24
    • 0035800734 scopus 로고    scopus 로고
    • The role of cholesterol and glycosylphosphatidylinositol-anchored proteins of erythrocyte rafts in regulating raft protein content and malarial infection
    • Samuel BU, Mohandas N, Harrison T, McManus H, Rosse W, Reid M, Haldar K. The role of cholesterol and glycosylphosphatidylinositol-anchored proteins of erythrocyte rafts in regulating raft protein content and malarial infection. Journal of Biological Chemistry 2001; 276: 29319-29
    • (2001) Journal of Biological Chemistry , vol.276 , pp. 29319-29329
    • Samuel, B.U.1    Mohandas, N.2    Harrison, T.3    McManus, H.4    Rosse, W.5    Reid, M.6    Haldar, K.7
  • 25
    • 0030840793 scopus 로고    scopus 로고
    • Oleanolic acid and ursolic acid stabilize liposomal membranes
    • Han SK, Ko YI, Park SJ, Jin IJ, Kim YM. Oleanolic acid and ursolic acid stabilize liposomal membranes. Lipids 1997; 32: 769-73
    • (1997) Lipids , vol.32 , pp. 769-773
    • Han, S.K.1    Ko, Y.I.2    Park, S.J.3    Jin, I.J.4    Kim, Y.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.