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Volumn 57, Issue 2, 1997, Pages 139-144

Anti-oedematous activities of the main triterpendiol esters of marigold (Calendula officinalis L.)

Author keywords

Anti oedematous activity; Calendula officinalis L.; Faradiol 3 myristic acid ester; Faradiol 3 palmitic acid ester; Marigold; Taraxasterol; Triterpendiol esters

Indexed keywords

CALENDULA EXTRACT; INDOMETACIN; TARAXASTEROL; TRITERPENE DERIVATIVE;

EID: 0030745007     PISSN: 03788741     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-8741(97)00061-5     Document Type: Article
Times cited : (140)

References (18)
  • 1
    • 0012116866 scopus 로고    scopus 로고
    • Topical anti-inflammatory activity of Calendula officinalis extracts
    • Della Loggia, R., Becker, H., Isaac, O., Tubaro, A., Topical anti-inflammatory activity of Calendula officinalis extracts. Planta Medica 56, 658.
    • Planta Medica , vol.56 , pp. 658
    • Della Loggia, R.1    Becker, H.2    Isaac, O.3    Tubaro, A.4
  • 2
    • 0028125141 scopus 로고
    • The role of triterpenoids in the topical anti-inflammatory activity of Calendula officinalis flowers
    • Della Loggia, R., Tubaro, A., Sosa, S., Becker, H., Saar, St., Isaa, O., 1994. The role of triterpenoids in the topical anti-inflammatory activity of Calendula officinalis flowers. Planta Medica 60, 516-520.
    • (1994) Planta Medica , vol.60 , pp. 516-520
    • Della Loggia, R.1    Tubaro, A.2    Sosa, S.3    Becker, H.4    Saar, St.5    Isaa, O.6
  • 4
    • 49549159866 scopus 로고
    • The stereochemical dependence of 13C chemical shifts in olean-12-enes and urs-12-enes as an aid to structural assignment
    • Doddrell, D.M., Khong, P.W., Lewis, K.G., 1974. The stereochemical dependence of 13C chemical shifts in olean-12-enes and urs-12-enes as an aid to structural assignment. Tetrahedron Letters 27, 2381-2384.
    • (1974) Tetrahedron Letters , vol.27 , pp. 2381-2384
    • Doddrell, D.M.1    Khong, P.W.2    Lewis, K.G.3
  • 5
    • 0002794758 scopus 로고
    • Wissenschaftliche Verlagsgesellschaft Stuttgart
    • Isaac, O., 1992 Die Ringelblume. Wissenschaftliche Verlagsgesellschaft Stuttgart, pp. 71-74.
    • (1992) Die Ringelblume , pp. 71-74
    • Isaac, O.1
  • 6
    • 0004831969 scopus 로고
    • Calendula officinalis L. - Die Ringelblume, Portrait einer Arzneipflanze
    • Isaac, O., 1994. Calendula officinalis L. - Die Ringelblume, Portrait einer Arzneipflanze. Zeitschrift für Phytotherapie 16, 357-370.
    • (1994) Zeitschrift für Phytotherapie , vol.16 , pp. 357-370
    • Isaac, O.1
  • 7
    • 0000154020 scopus 로고
    • Triterpenic alcohols of Calendula officinalis L. flowers
    • Kasprzyk, Z., Pyrek, J., 1968. Triterpenic alcohols of Calendula officinalis L. flowers. Phytochemistry 7, 1631-1639.
    • (1968) Phytochemistry , vol.7 , pp. 1631-1639
    • Kasprzyk, Z.1    Pyrek, J.2
  • 9
    • 0004633591 scopus 로고
    • Cutaneous cicatrization after topic application of calendulas cream and comfrey, propolis and honey associations in infected wound of skin
    • Sao Paulo
    • Perri de Carvalho, P.S., Tagliavini, D.G., Tagliavini, R.L., 1991. Cutaneous cicatrization after topic application of calendulas cream and comfrey, propolis and honey associations in infected wound of skin. Revista Ciência Biomédica (Sao Paulo) 12, 39-50.
    • (1991) Revista Ciência Biomédica , vol.12 , pp. 39-50
    • Perri De Carvalho, P.S.1    Tagliavini, D.G.2    Tagliavini, R.L.3
  • 10
    • 0019719565 scopus 로고
    • Propriétés anti-oedémateuses et anti-hyperhémiantes du Calendula officinalis L
    • Peyrox, J., Rossignol, P., Delaveau, P., 1981. Propriétés anti-oedémateuses et anti-hyperhémiantes du Calendula officinalis L.. Plantes Médicinales et Phytothérapie 15, 210-216.
    • (1981) Plantes Médicinales et Phytothérapie , vol.15 , pp. 210-216
    • Peyrox, J.1    Rossignol, P.2    Delaveau, P.3
  • 11
    • 25444434764 scopus 로고
    • Faradiol and arnidiol - Revision of the structure
    • Pyrek, J.St., Baranowska, E., 1973. Faradiol and arnidiol - revision of the structure. Tetrahedron Letters 11, 809-810.
    • (1973) Tetrahedron Letters , vol.11 , pp. 809-810
    • Pyrek, J.St.1    Baranowska, E.2
  • 12
    • 3242690216 scopus 로고
    • Total assignment of 13C and 1H spectra of three isomeric triterpenol derivatives by 2D NMR: An investigation of the potential utility of 1H chemical shifts in structural investigations of complex natural products
    • Reynolds, W.F., McLean, S., Poplawski, J., 1986. Total assignment of 13C and 1H spectra of three isomeric triterpenol derivatives by 2D NMR: An investigation of the potential utility of 1H chemical shifts in structural investigations of complex natural products. Tetrahedron 42, 3419-3428.
    • (1986) Tetrahedron , vol.42 , pp. 3419-3428
    • Reynolds, W.F.1    McLean, S.2    Poplawski, J.3
  • 14
    • 0019740888 scopus 로고
    • Study on the anti-inflammatory effect of a group of plant extracts
    • Sofia
    • Shipochliev, T., Dimitrov, A., Aleksandrova, E., 1981. Study on the anti-inflammatory effect of a group of plant extracts. Veterinary Sciences (Sofia) 18, 87-94.
    • (1981) Veterinary Sciences , vol.18 , pp. 87-94
    • Shipochliev, T.1    Dimitrov, A.2    Aleksandrova, E.3
  • 16
    • 84986870106 scopus 로고
    • Carbon-13 nuclear magnetic resonance spectroscopy of naturally-occurring substances
    • Wenkert, E., Baddeley, G.V., Burfitt, I.R., Moreno, L.N., 1978. Carbon-13 nuclear magnetic resonance spectroscopy of naturally-occurring substances. Organic Magnetic Resonance 11, 337-342.
    • (1978) Organic Magnetic Resonance , vol.11 , pp. 337-342
    • Wenkert, E.1    Baddeley, G.V.2    Burfitt, I.R.3    Moreno, L.N.4
  • 17
    • 0003886432 scopus 로고
    • Free and ester-bound triterpene alcohols and sterols in cellular subfractions of Calendula officinalis flowers
    • Wilkomirski, B., Kasprzyk, Z., 1979. Free and ester-bound triterpene alcohols and sterols in cellular subfractions of Calendula officinalis flowers. Phytochemistry 18, 253-255.
    • (1979) Phytochemistry , vol.18 , pp. 253-255
    • Wilkomirski, B.1    Kasprzyk, Z.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.