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Volumn 36, Issue 18, 2011, Pages 2511-2514

Triterpenes and sterols from Nauclea latifolia

Author keywords

Guinea; Nauclea latifolia; Rubiaceae; Triterpenes and sterols

Indexed keywords

24 EN CYCLOARTENONE; DAUCOSTEROL; EBETA,19ALPHA,23,24 TETRAHYDROXYURS 12 EN 28 OIC ACID; NAUCLEA LATIFOLIA EXTRACT; PYROCINCHOLIC ACID 3BETA O BETA DEXTRO FUCOPYRANOSIDE; QUINOVIC ACID; QUINOVIC ACID 3B O DEXTRO GLUCOPYRANOSYL (28-1) BETA DEXTRO GLUCOPYRANOSYL ESTER; QUINOVIC ACID 3BETA O BETA DEXTRO GLUCOPYRANOSIDE; ROTUNDIC ACID; SILICA GEL; SITOSTEROL; STEROL DERIVATIVE; STIGMAST 4 EN 6BETA OL 3 ONE; STIGMASTAN 3,6 DIONE; TRITERPENE DERIVATIVE; UNCLASSIFIED DRUG; URSOLIC ALDEHYDE;

EID: 83055167073     PISSN: 10015302     EISSN: None     Source Type: Journal    
DOI: 10.4268/cjcmm20111813     Document Type: Article
Times cited : (11)

References (13)
  • 1
    • 67849116715 scopus 로고    scopus 로고
    • Anticonvulsant, anxiolytic, and sedative properties of the roots of Nauclea latifolia Smith in mice
    • J
    • Ngo Bum E, Taiwe G S, Moto F C O, et al. Anticonvulsant, anxiolytic, and sedative properties of the roots of Nauclea latifolia Smith in mice[J]. Epilepsy Behav, 2009,15(4):434.
    • (2009) Epilepsy Behav , vol.15 , Issue.4 , pp. 434
    • Ngo Bum, E.1    Taiwe, G.S.2    Moto, F.C.O.3
  • 2
    • 83055191028 scopus 로고    scopus 로고
    • Chinese source
  • 3
    • 83055191027 scopus 로고    scopus 로고
    • Chinese source
  • 4
    • 83055165099 scopus 로고    scopus 로고
    • Study on chemical composition of Nauclea Officinalis Leaves
    • J
    • Su K, Gong M, Zhou J, et al. Study on chemical composition of Nauclea Officinalis Leaves[J]. Int J Chem, 2009,1(2):77.
    • (2009) Int J Chem , vol.1 , Issue.2 , pp. 77
    • Su, K.1    Gong, M.2    Zhou, J.3
  • 5
    • 23844501075 scopus 로고    scopus 로고
    • Triterpenoids from the flower of Campsis grandiflora K. Schum. as human acyl-CoA: Cholesterol acyltransferase inhibitors
    • J
    • Kim D H, Han K M, Chung I S, et al. Triterpenoids from the flower of Campsis grandiflora K. Schum. as human acyl-CoA: cholesterol acyltransferase inhibitors[J]. Arch Pharm Res, 2005,28(5):550.
    • (2005) Arch Pharm Res , vol.28 , Issue.5 , pp. 550
    • Kim, D.H.1    Han, K.M.2    Chung, I.S.3
  • 6
    • 0036599582 scopus 로고    scopus 로고
    • Structure-activity relationship of triterpenoids isolated from Mitragyna stipulosa on cytotoxicity
    • J
    • Leon Azefack Tapondjou, David Lontsi, Beiham Luc Sondengam, et al. Structure-activity relationship of triterpenoids isolated from Mitragyna stipulosa on cytotoxicity[J], Arch Pharm Res, 2002,25(3):270.
    • (2002) Arch Pharm Res , vol.25 , Issue.3 , pp. 270
    • Tapondjou, L.A.1    Lontsi, D.2    Sondengam, B.L.3
  • 7
    • 83055191026 scopus 로고    scopus 로고
    • Chinese source
  • 8
    • 83055165108 scopus 로고    scopus 로고
    • Chinese source
  • 9
    • 0029964579 scopus 로고    scopus 로고
    • Triterpenoids from Adina rubella
    • J
    • Fang S Y, He Z S, Fan G J, et al. Triterpenoids from Adina rubella[J]. J Nat Prod, 1996,59(3):304.
    • (1996) J Nat Prod , vol.59 , Issue.3 , pp. 304
    • Fang, S.Y.1    He, Z.S.2    Fan, G.J.3
  • 10
    • 83055185881 scopus 로고    scopus 로고
    • Chinese source
  • 11
    • 0343051943 scopus 로고    scopus 로고
    • Triterpenoid Saponins from the Roots of Zygophyllum Species
    • J
    • Karl Pollmann, Stefan Gagel, MHani A Elgamal, et al. Triterpenoid Saponins from the Roots of Zygophyllum Species[J]. Phytochemistry,1997,44(3): 485.
    • (1997) Phytochemistry , vol.44 , Issue.3 , pp. 485
    • Pollmann, K.1    Gagel, S.2    Hani, M.3    Elgamal, A.4
  • 12
    • 83055191025 scopus 로고    scopus 로고
    • Chinese source
  • 13
    • 0025646673 scopus 로고
    • Stigmasterols from Typha Latifolia
    • J
    • Marina Della Greca, Pietro Monaco, Lucio Previtera. Stigmasterols from Typha Latifolia[J]. J Nat Prod, 1990,53(6):1430.
    • (1990) J Nat Prod , vol.53 , Issue.6 , pp. 1430
    • Greca, M.D.1    Monaco, P.2    Previtera, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.