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Volumn 1, Issue 4, 2008, Pages 183-187

Polyhydroxyoleanane-type triterpenoids from Combretum molle and their anti-inflammatory activity

Author keywords

Anti inflammatory activity; Combretaceae; Combretum molle; Saponins; Triterpenoid

Indexed keywords

ARJUNGENIN; ARJUNGLUCOSIDE; BETA D GLUCOPYRANOSYL 2ALPHA,3BETA,6BETA TRIHYDROXY 23 GALLOYLOLEAN 12 EN 28 OATE; CARBON 13; CARRAGEENAN; COMBREGENIN; COMBREGLUCOSIDE; COMBRETUM MOLLE EXTRACT; INDOMETACIN; PLANT EXTRACT; PROTON; TRITERPENOID; UNCLASSIFIED DRUG;

EID: 56349147805     PISSN: 18743900     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.phytol.2008.09.002     Document Type: Article
Times cited : (35)

References (24)
  • 1
    • 0026940759 scopus 로고
    • NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides
    • Agrawal P.K. NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides. Phytochemistry 31 (1992) 3307-3330
    • (1992) Phytochemistry , vol.31 , pp. 3307-3330
    • Agrawal, P.K.1
  • 2
    • 0036270557 scopus 로고    scopus 로고
    • Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis
    • Ahn M.J., Kim C.Y., Lee J.S., Kim T.G., Kim S.H., Lee C.K., Lee B.B., Shin C.G., Huh H., and Kim J. Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis. Planta Med. 68 (2002) 457-459
    • (2002) Planta Med. , vol.68 , pp. 457-459
    • Ahn, M.J.1    Kim, C.Y.2    Lee, J.S.3    Kim, T.G.4    Kim, S.H.5    Lee, C.K.6    Lee, B.B.7    Shin, C.G.8    Huh, H.9    Kim, J.10
  • 3
    • 0034764924 scopus 로고    scopus 로고
    • In vitro antiprotozoal activity of extract and compounds from the stem bark of Combretum molle
    • Ares K., Bucar F., Knauder E., Yardlev V., Kendrick H., and Croft S.L. In vitro antiprotozoal activity of extract and compounds from the stem bark of Combretum molle. Phytother. Res. 15 (2001) 613-617
    • (2001) Phytother. Res. , vol.15 , pp. 613-617
    • Ares, K.1    Bucar, F.2    Knauder, E.3    Yardlev, V.4    Kendrick, H.5    Croft, S.L.6
  • 4
    • 15444378957 scopus 로고    scopus 로고
    • In vitro activity of three selected South African medicinal plants against human immunodeficiency virus type 1 reverse transcriptase
    • Bessong P.O., Obi C.L., Igumbor E., Andreola M.-L., and Litvak S. In vitro activity of three selected South African medicinal plants against human immunodeficiency virus type 1 reverse transcriptase. Afr. J. Biotechnol. 3 (2004) 555-559
    • (2004) Afr. J. Biotechnol. , vol.3 , pp. 555-559
    • Bessong, P.O.1    Obi, C.L.2    Igumbor, E.3    Andreola, M.-L.4    Litvak, S.5
  • 6
    • 0020027340 scopus 로고
    • Molluscicidal properties of various saponins
    • Hostettmann K., Kizu H., and Tominori T. Molluscicidal properties of various saponins. Planta Med. 44 (1982) 34-35
    • (1982) Planta Med. , vol.44 , pp. 34-35
    • Hostettmann, K.1    Kizu, H.2    Tominori, T.3
  • 7
  • 8
    • 18444385661 scopus 로고    scopus 로고
    • 19α-Hydroxyursane-type triterpenoids: antinociceptive, anti-inflammatory principles of the roots of Rosa rugosa
    • Jung H.J., Nam J.H., Choi J., Lee K.T., and Park H.J. 19α-Hydroxyursane-type triterpenoids: antinociceptive, anti-inflammatory principles of the roots of Rosa rugosa. Biol. Pharm. Bull. 28 (2005) 101-104
    • (2005) Biol. Pharm. Bull. , vol.28 , pp. 101-104
    • Jung, H.J.1    Nam, J.H.2    Choi, J.3    Lee, K.T.4    Park, H.J.5
  • 9
    • 0036549816 scopus 로고    scopus 로고
    • In vitro anti-inflammatory activity of Kalopanaxsaponin A isolated from Kalopanax pictus in murine macrophage raw 264.7 cells
    • Kim Y.K., Kim R.G., Park S.J., Ha J.H., Choi J.W., Park H.J., and Lee K.T. In vitro anti-inflammatory activity of Kalopanaxsaponin A isolated from Kalopanax pictus in murine macrophage raw 264.7 cells. Biol. Pharm. Bull. 25 (2002) 472-476
    • (2002) Biol. Pharm. Bull. , vol.25 , pp. 472-476
    • Kim, Y.K.1    Kim, R.G.2    Park, S.J.3    Ha, J.H.4    Choi, J.W.5    Park, H.J.6    Lee, K.T.7
  • 10
    • 0001307676 scopus 로고
    • Triterpenoids and their glycosides from Terminalia chebula
    • Kundu A.P., and Mahato S.B. Triterpenoids and their glycosides from Terminalia chebula. Phytochemistry 32 (1993) 999-1002
    • (1993) Phytochemistry , vol.32 , pp. 999-1002
    • Kundu, A.P.1    Mahato, S.B.2
  • 11
    • 0025905444 scopus 로고
    • Analgesic, antipyretic and anti-inflammatory properties of Euphorbia hirta
    • Lanhers M.C., Fleurentin J., Dorfman P., Motrier F., and Pelt J.M. Analgesic, antipyretic and anti-inflammatory properties of Euphorbia hirta. Planta Med. 57 (1991) 225-231
    • (1991) Planta Med. , vol.57 , pp. 225-231
    • Lanhers, M.C.1    Fleurentin, J.2    Dorfman, P.3    Motrier, F.4    Pelt, J.M.5
  • 12
    • 0034089427 scopus 로고    scopus 로고
    • Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bidesmosides isolated from the stem bark of Kolopanax pictus
    • Lee K.T., Sohn I.C., Park H.J., Kim D.W.W., Jung G.O., and Park K.Y. Essential moiety for antimutagenic and cytotoxic activity of hederagenin monodesmosides and bidesmosides isolated from the stem bark of Kolopanax pictus. Planta Med. 66 (2000) 329-332
    • (2000) Planta Med. , vol.66 , pp. 329-332
    • Lee, K.T.1    Sohn, I.C.2    Park, H.J.3    Kim, D.W.W.4    Jung, G.O.5    Park, K.Y.6
  • 14
    • 0028248808 scopus 로고
    • 13C NMR spectra of pentacyclic triterpenoids, a compilation and some salient features
    • 13C NMR spectra of pentacyclic triterpenoids, a compilation and some salient features. Phytochemistry 37 (1994) 1517-1575
    • (1994) Phytochemistry , vol.37 , pp. 1517-1575
    • Mahato, S.B.1    Kundu, A.P.2
  • 15
    • 0000790396 scopus 로고
    • Scyllo-quercitol gallates and hexahydroxydiphenoates from Quercus stenophylla
    • Nishimura H., Nonaka G.I., and Nishioka I. Scyllo-quercitol gallates and hexahydroxydiphenoates from Quercus stenophylla. Phytochemistry 25 (1986) 2599-2604
    • (1986) Phytochemistry , vol.25 , pp. 2599-2604
    • Nishimura, H.1    Nonaka, G.I.2    Nishioka, I.3
  • 16
    • 0001184768 scopus 로고
    • Identification of mollic acid α-l-arabinoside, α-hydroxycycloartenoid from Combretum molle leaves
    • Rogers C.B., and Thevan I. Identification of mollic acid α-l-arabinoside, α-hydroxycycloartenoid from Combretum molle leaves. Phytochemistry 25 (1986) 1759-1761
    • (1986) Phytochemistry , vol.25 , pp. 1759-1761
    • Rogers, C.B.1    Thevan, I.2
  • 21
    • 0019167692 scopus 로고
    • Research of antifungal from several active principe extracts from climbing-ivy: Hedera helix
    • Timon D., Julien P.J., Gasquet M., Balansard G., and Bernard P. Research of antifungal from several active principe extracts from climbing-ivy: Hedera helix. Ann. Pharm. Fr. 38 (1980) 545-552
    • (1980) Ann. Pharm. Fr. , vol.38 , pp. 545-552
    • Timon, D.1    Julien, P.J.2    Gasquet, M.3    Balansard, G.4    Bernard, P.5
  • 22
    • 67249094291 scopus 로고
    • Carrageenan-induced oedema in hind paws of the rats as an assay for anti-inflammatory drugs
    • Winter C.A., Risley E.A., and Nuss G.W. Carrageenan-induced oedema in hind paws of the rats as an assay for anti-inflammatory drugs. Proc. Soc. Exp. Biol. Med. 111 (1962) 544-547
    • (1962) Proc. Soc. Exp. Biol. Med. , vol.111 , pp. 544-547
    • Winter, C.A.1    Risley, E.A.2    Nuss, G.W.3
  • 23
    • 33646458073 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationship study of antidiabetic penta-o-galloyl-d-glucopyranose and its analogues
    • Yulin R., Himmeldirk K., and Xiaozhuo C. Synthesis and structure-activity relationship study of antidiabetic penta-o-galloyl-d-glucopyranose and its analogues. J. Med. Chem. 49 (2006) 2829-2837
    • (2006) J. Med. Chem. , vol.49 , pp. 2829-2837
    • Yulin, R.1    Himmeldirk, K.2    Xiaozhuo, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.