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Volumn 74, Issue 14, 2008, Pages 1741-1744

Cytotoxic cucurbitane-type triterpenoids from Elaeocarpus hainanensis

Author keywords

Cucurbitane; Cytotoxicity; Elaeocarpaceae; Elaeocarpus hainanensis; Triterpenoids

Indexed keywords

16ALPHA,23ALPHA EPOXY 20BETA,25 DIHYDROXY 10ALPHAH,23BETAH CUCURBIT 5 EN 11 ONE 3 O BETA GLUCOPYRANOSIDE; 16ALPHA,23ALPHA EPOXY 3BETA,10BETA DIHYDROXY 10ALPHAH,23BETAH CUCURBIT 5,24 DIEN 11 ONE; 16ALPHA,23ALPHA EPOXY 3BETA,20BETA DIHYDROXY 10ALPHAH,23BETAH CUCURBIT 5,24 DIEN 11 ONE 2 O BETA GLUCOPYRANOSIDE; 19 NORLANOSTA 5,24 DIEN 11 ONE; 3 EPI ISOCUCURBITACIN G; CUCURBITACIN; CUCURBITACIN D; CUCURBITACIN F; CUCURBITACIN G; CUCURBITACIN I; CUCURBITACIN O; TRITERPENOID; UNCLASSIFIED DRUG;

EID: 57149119928     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1081356     Document Type: Article
Times cited : (30)

References (20)
  • 1
    • 0042844744 scopus 로고    scopus 로고
    • Natural products sources of new drugs over the period 1981-2002
    • Newman DJ, Cragg CM, Snader KM. Natural products sources of new drugs over the period 1981-2002. J Nat Prod 2003; 66: 1022-37
    • (2003) J Nat Prod , vol.66 , pp. 1022-1037
    • Newman, D.J.1    Cragg, C.M.2    Snader, K.M.3
  • 2
    • 57149094463 scopus 로고    scopus 로고
    • South China Botanical Garden CAS
    • Fisheries and Conservation Department;
    • Hong Kong Herbarium, South China Botanical Garden CAS. Check list of Hong Kong plants Hong Kong: Agriculture, Fisheries and Conservation Department; 2001: 75
    • (2001) Check list of Hong Kong plants Hong Kong: Agriculture , pp. 75
    • Hong, K.1
  • 5
    • 14544300945 scopus 로고    scopus 로고
    • Grandisine A and B, novel indolizidine alkaloids with human δ-opioid receptor binding affinity from the leaves of the Australian rainforest tree Elaeocarpus grandis
    • Carroll AR, Arumugan G, Quinn RJ, Redburn J, Guymer G, Grimshaw P. Grandisine A and B, novel indolizidine alkaloids with human δ-opioid receptor binding affinity from the leaves of the Australian rainforest tree Elaeocarpus grandis. J Org Chem 2005; 70: 1889-92
    • (2005) J Org Chem , vol.70 , pp. 1889-1892
    • Carroll, A.R.1    Arumugan, G.2    Quinn, R.J.3    Redburn, J.4    Guymer, G.5    Grimshaw, P.6
  • 6
    • 33750030763 scopus 로고    scopus 로고
    • Grandisines C-G, indolizidine alkaloids from the Australian rainforest tree Elaeocarpus grandis
    • Katavic PL, Venables DA, Forster PI, Guymer G, Carroll AR. Grandisines C-G, indolizidine alkaloids from the Australian rainforest tree Elaeocarpus grandis. J Nat Prod 2006; 69: 1295-9
    • (2006) J Nat Prod , vol.69 , pp. 1295-1299
    • Katavic, P.L.1    Venables, D.A.2    Forster, P.I.3    Guymer, G.4    Carroll, A.R.5
  • 7
    • 34250742515 scopus 로고    scopus 로고
    • Habbemines A and B, pyrrolidine alkaloids with human δ-opioid receptor binding affinity from the leaves of Elaeocarpus habbemensis
    • Katavic PL, Venables DA, Rali T, Carroll AR. Habbemines A and B, pyrrolidine alkaloids with human δ-opioid receptor binding affinity from the leaves of Elaeocarpus habbemensis. J Nat Prod 2007; 70: 866-8
    • (2007) J Nat Prod , vol.70 , pp. 866-868
    • Katavic, P.L.1    Venables, D.A.2    Rali, T.3    Carroll, A.R.4
  • 8
    • 34250705819 scopus 로고    scopus 로고
    • Indolizidine alkaloids with δ-opioid receptor binding affinity from the leaves of Elaeocorpus fuscoides
    • Katavic PL, Venables DA, Rali T, Carroll AR. Indolizidine alkaloids with δ-opioid receptor binding affinity from the leaves of Elaeocorpus fuscoides. J Nat Prod 2007; 70: 72-5
    • (2007) J Nat Prod , vol.70 , pp. 72-75
    • Katavic, P.L.1    Venables, D.A.2    Rali, T.3    Carroll, A.R.4
  • 11
    • 24044499948 scopus 로고    scopus 로고
    • NMR signal assignment of 22-deoxocucurbitacin D and cucurbitacin D from Ecballium elaterium L. (Cucurbitaceae)
    • Seger C, Sturm S, Haslinger E, Stuppner H. NMR signal assignment of 22-deoxocucurbitacin D and cucurbitacin D from Ecballium elaterium L. (Cucurbitaceae). Monatsheft Chem 2005; 136: 1645-9
    • (2005) Monatsheft Chem , vol.136 , pp. 1645-1649
    • Seger, C.1    Sturm, S.2    Haslinger, E.3    Stuppner, H.4
  • 12
    • 0032920365 scopus 로고    scopus 로고
    • Ecdysteroid antagonists (cucurbitacins) from Physocarpus opulifolius (Rosaceae)
    • Sarker SD, Whiting P, ik V, Dinan L. Ecdysteroid antagonists (cucurbitacins) from Physocarpus opulifolius (Rosaceae). Phytochemistry 1999; 50: 1123-8
    • (1999) Phytochemistry , vol.50 , pp. 1123-1128
    • Sarker, S.D.1    Whiting, P.2    ik, V.3    Dinan, L.4
  • 14
    • 0029152696 scopus 로고    scopus 로고
    • Fujita S, Kasai R, Ohtani K, Yamasaki K, Chiu MH, Nie RL et al. Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola. Phyto-chemistry 1995; 38: 465-72
    • Fujita S, Kasai R, Ohtani K, Yamasaki K, Chiu MH, Nie RL et al. Dammarane glycosides from aerial parts of Neoalsomitra integrifoliola. Phyto-chemistry 1995; 38: 465-72
  • 15
  • 16
    • 0020679388 scopus 로고
    • 13C-NMR spectroscopy of cucurbitacins
    • 13C-NMR spectroscopy of cucurbitacins. Tetrahedron 1983; 39: 317-21
    • (1983) Tetrahedron , vol.39 , pp. 317-321
    • Velde, W.1    Lavie, D.2
  • 19
    • 21244470815 scopus 로고    scopus 로고
    • Cucurbitacins and cucurbitane glycosides: Structures and biological activities
    • Chen JC, Chiu MH, Nie RL, Cordell GA, Qiu SX. Cucurbitacins and cucurbitane glycosides: structures and biological activities. Nat Prod Rep 2005; 22: 386-99
    • (2005) Nat Prod Rep , vol.22 , pp. 386-399
    • Chen, J.C.1    Chiu, M.H.2    Nie, R.L.3    Cordell, G.A.4    Qiu, S.X.5
  • 20
    • 0025775062 scopus 로고
    • Feasibility of a high-flux anticancer drug screen utilizing a diverse panel of human tumor cell lines in culture
    • Monks A, Scudiero D, Skehan P, Shoemaker R, Paull K, Vistica D et al. Feasibility of a high-flux anticancer drug screen utilizing a diverse panel of human tumor cell lines in culture. J Natl Cancer Inst 1991; 83: 757-66
    • (1991) J Natl Cancer Inst , vol.83 , pp. 757-766
    • Monks, A.1    Scudiero, D.2    Skehan, P.3    Shoemaker, R.4    Paull, K.5    Vistica, D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.