메뉴 건너뛰기




Volumn 36, Issue 3, 2013, Pages 322-326

Three new nor-dammarane triterpenoids from Dysoxylum hainanense with particular cytotoxicity against glioma cell line

Author keywords

Cytotoxicity; Dysoxylum hainanense; Meliaceae; Nor dammarane triterpenoids

Indexed keywords

12BETA HYDROXY 3,15 DIOXO 20,21,22,23,24,25,26,27 OCTANORDAMMANRAN; 12BETA O ACETYL 15ALPHA HYDOXY 3 OXO 17 EN 20,21,22,23,24,25,26,27 OCTANORDAMMANRAN; 12BETA O ACETYL 15ALPHA,28 DIHYDOXY 3 OXO 17 EN 20,21,22,23,24,25,26,27 OCTANORDAMMANRAN; 12BETA,28 O DIACETYL 15ALPHA HYDOXY 3 OXO 17 EN 20,21,22,23,24,25,26,27 OCTANORDAMMANRAN; TRITERPENOID; UNCLASSIFIED DRUG;

EID: 84879551852     PISSN: 02536269     EISSN: 19763786     Source Type: Journal    
DOI: 10.1007/s12272-013-0030-9     Document Type: Article
Times cited : (11)

References (13)
  • 1
    • 0000804512 scopus 로고
    • Dammarane triterpenoids from the fruits of Dysoxylum richii
    • 10.1016/0031-9422(91)85280-D
    • Albersberg, W., and Y. Singh. 1991. Dammarane triterpenoids from the fruits of Dysoxylum richii. Phytochemistry 30: 921-926.
    • (1991) Phytochemistry , vol.30 , pp. 921-926
    • Albersberg, W.1    Singh, Y.2
  • 2
    • 0031031683 scopus 로고    scopus 로고
    • Antitumor agents. 168. Dysoxylum cumingianum. IV. The structures of cumingianosides G-O, new triterpene glucosides with a 14,18-cycloapotirucallane- type skeleton from Dysoxylum cumingianum, and their cytotoxicity against human cancer cell lines
    • 10.1248/cpb.45.68 1:CAS:528:DyaK2sXotV2qtg%3D%3D
    • Fujioka, T., A. Sakurai, K. Mihashi, Y. Kashiwada, I.S. Chen, and K.H. Lee. 1997. Antitumor agents. 168. Dysoxylum cumingianum. IV. The structures of cumingianosides G-O, new triterpene glucosides with a 14,18-cycloapotirucallane- type skeleton from Dysoxylum cumingianum, and their cytotoxicity against human cancer cell lines. Chemical and Pharmaceutical Bulletin 45: 68-74.
    • (1997) Chemical and Pharmaceutical Bulletin , vol.45 , pp. 68-74
    • Fujioka, T.1    Sakurai, A.2    Mihashi, K.3    Kashiwada, Y.4    Chen, I.S.5    Lee, K.H.6
  • 3
    • 0031041663 scopus 로고    scopus 로고
    • Ergosta-5,24(24′)-diene-3β,4β,20S-triol, an ergostane steroid from Dysoxylum malabaricum
    • 10.1016/S0031-9422(96)00462-1 1:CAS:528:DyaK2sXhsVanug%3D%3D
    • Govindachari, T.R., K.G.N. Kumari, and G. Suresh. 1997. Ergosta-5,24(24′)-diene-3β,4β,20S-triol, an ergostane steroid from Dysoxylum malabaricum. Phytochemistry 44: 153-155.
    • (1997) Phytochemistry , vol.44 , pp. 153-155
    • Govindachari, T.R.1    Kumari, K.G.N.2    Suresh, G.3
  • 4
    • 0028008973 scopus 로고
    • Triterpenoids from Dysoxylum malabaricum
    • 10.1016/S0031-9422(00)89542-4 1:CAS:528:DyaK2MXitFyksbY%3D
    • Govindachari, T.R., G. Suresh, and K.G.N. Kumari. 1994. Triterpenoids from Dysoxylum malabaricum. Phytochemistry 37: 1127-1129.
    • (1994) Phytochemistry , vol.37 , pp. 1127-1129
    • Govindachari, T.R.1    Suresh, G.2    Kumari, K.G.N.3
  • 5
    • 78650517608 scopus 로고    scopus 로고
    • Ring A-seco triterpenoids with antibacterial activity from Dysoxylum hainanense
    • 21131198 10.1016/j.bmcl.2010.11.057 1:CAS:528:DC%2BC3cXhs1SqsLnF
    • He, X.F., X.N. Wang, S. Yin, L. Dong, and J.M. Yue. 2011. Ring A-seco triterpenoids with antibacterial activity from Dysoxylum hainanense. Bioorganic and Medicinal Chemistry Letters 21: 125-129.
    • (2011) Bioorganic and Medicinal Chemistry Letters , vol.21 , pp. 125-129
    • He, X.F.1    Wang, X.N.2    Yin, S.3    Dong, L.4    Yue, J.M.5
  • 6
    • 0000521670 scopus 로고
    • Dysoxylin, a limonoid from Dysoxylum richii
    • 10.1016/S0031-9422(00)82494-2 1:CAS:528:DyaL1cXitFyqt74%3D
    • Jogia, M.K., and R.J. Andersen. 1987. Dysoxylin, a limonoid from Dysoxylum richii. Phytochemistry 26: 3309-3311.
    • (1987) Phytochemistry , vol.26 , pp. 3309-3311
    • Jogia, M.K.1    Andersen, R.J.2
  • 7
    • 82455195878 scopus 로고    scopus 로고
    • Bioactivity of the compounds in genus Dysoxylum
    • 10.1016/j.chnaes.2009.04.005
    • Lakshmi, V., K. Pandey, and S.K. Agarwal. 2009. Bioactivity of the compounds in genus Dysoxylum. Acta Ecologica Sinica 29: 30-44.
    • (2009) Acta Ecologica Sinica , vol.29 , pp. 30-44
    • Lakshmi, V.1    Pandey, K.2    Agarwal, S.K.3
  • 8
    • 62549156228 scopus 로고    scopus 로고
    • Bioactivity-guided isolation of cytotoxic constituents of Brucea javanica collected in Vietnam
    • 19026551 10.1016/j.bmc.2008.10.076 1:CAS:528:DC%2BD1MXjsFWqtLg%3D
    • Pan, L., Y.W. Chin, H.B. Chai, T.N. Ninh, D.D. Soejarto, and A.D. Kinghorn. 2009. Bioactivity-guided isolation of cytotoxic constituents of Brucea javanica collected in Vietnam. Bioorganic and Medicinal Chemistry 17: 2219-2224.
    • (2009) Bioorganic and Medicinal Chemistry , vol.17 , pp. 2219-2224
    • Pan, L.1    Chin, Y.W.2    Chai, H.B.3    Ninh, T.N.4    Soejarto, D.D.5    Kinghorn, A.D.6
  • 9
    • 77956676720 scopus 로고    scopus 로고
    • Two new cytotoxic isomeric indole alkaloids from the roots of Nauclea orientalis
    • 20472039 10.1016/j.fitote.2010.05.004 1:CAS:528:DC%2BC3cXhtFCrtLbK
    • Sichaem, J., S. Surapinit, P. Siripong, S. Khumkratok, J. Jong-aramruang, and S. Tip-pyang. 2010. Two new cytotoxic isomeric indole alkaloids from the roots of Nauclea orientalis. Fitoterapia 81: 830-833.
    • (2010) Fitoterapia , vol.81 , pp. 830-833
    • Sichaem, J.1    Surapinit, S.2    Siripong, P.3    Khumkratok, S.4    Jong-Aramruang, J.5    Tip-Pyang, S.6
  • 10
    • 0000856359 scopus 로고
    • Dammarane triterpenoids from Dysoxylum richii
    • 10.1016/S0031-9422(00)97581-2 1:CAS:528:DyaK3sXjsF2ntA%3D%3D
    • Singh, Y., and W. Aalbersberg. 1992. Dammarane triterpenoids from Dysoxylum richii. Phytochemistry 31: 4033-4035.
    • (1992) Phytochemistry , vol.31 , pp. 4033-4035
    • Singh, Y.1    Aalbersberg, W.2
  • 11
    • 0000240676 scopus 로고
    • Dysobinin, a new tetranortriterpene from Dysoxylum binectariferum
    • 10.1016/S0031-9422(00)88877-9 1:CAS:528:DyaE2sXhslWltrs%3D
    • Singh, S., H.S. Garg, and N.M. Khanna. 1976. Dysobinin, a new tetranortriterpene from Dysoxylum binectariferum. Phytochemistry 15: 2001-2002.
    • (1976) Phytochemistry , vol.15 , pp. 2001-2002
    • Singh, S.1    Garg, H.S.2    Khanna, N.M.3
  • 12
    • 83055184386 scopus 로고    scopus 로고
    • Cytotoxic nor-dammarane triterpenoids from Dysoxylum hainanense
    • 21856384 10.1016/j.fitote.2011.08.006 1:CAS:528:DC%2BC3MXhs1Sru7bJ
    • Wang, F., and Y.J. Guan. 2012. Cytotoxic nor-dammarane triterpenoids from Dysoxylum hainanense. Fitoterapia 83: 13-17.
    • (2012) Fitoterapia , vol.83 , pp. 13-17
    • Wang, F.1    Guan, Y.J.2
  • 13
    • 78249281345 scopus 로고    scopus 로고
    • Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia
    • 20851441 10.1016/j.phytochem.2010.08.017 1:CAS:528:DC%2BC3cXhsVagtb%2FI
    • Zhang, Y., J.S. Wang, D.D. Wei, X.B. Wang, J. Luo, J.G. Luo, and L.Y. Kong. 2010. Cytotoxic tirucallane C26 triterpenoids from the stem barks of Aphanamixis grandifolia. Phytochemistry 71: 2199-2204.
    • (2010) Phytochemistry , vol.71 , pp. 2199-2204
    • Zhang, Y.1    Wang, J.S.2    Wei, D.D.3    Wang, X.B.4    Luo, J.5    Luo, J.G.6    Kong, L.Y.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.