메뉴 건너뛰기




Volumn 49, Issue 2, 2006, Pages 693-708

Miliusanes, a class of cytotoxic agents from Miliusa sinensis

Author keywords

[No Author keywords available]

Indexed keywords

CYTOTOXIC AGENT; LACTONE; MILIUSANE; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 31544443011     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0509492     Document Type: Article
Times cited : (35)

References (14)
  • 3
    • 0035582364 scopus 로고    scopus 로고
    • New norditerpene from Miliusa balansae Finet et Gagnep
    • Wu, R.; Ye, Q.; Chen, N. Y.; Zhang, G. L. New norditerpene from Miliusa balansae Finet et Gagnep. Chin. Chem. Lett. 2001, 12, 247-248.
    • (2001) Chin. Chem. Lett. , vol.12 , pp. 247-248
    • Wu, R.1    Ye, Q.2    Chen, N.Y.3    Zhang, G.L.4
  • 4
    • 1642546963 scopus 로고    scopus 로고
    • Homogentisic acid derivatives from Miliusa balansae
    • Huong, D. T.; Kamperdick, C.; Sung, T. V. Homogentisic acid derivatives from Miliusa balansae. J. Nat. Prod. 2004, 67, 445-447.
    • (2004) J. Nat. Prod. , vol.67 , pp. 445-447
    • Huong, D.T.1    Kamperdick, C.2    Sung, T.V.3
  • 5
  • 6
    • 33947085552 scopus 로고
    • Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters
    • Dale, J. A.; Mosher, H. S. Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and α-methoxy-α- trifluoromethylphenylacetate (MTPA) esters. J. Am. Chem. Soc. 1973, 95, 512-519.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 512-519
    • Dale, J.A.1    Mosher, H.S.2
  • 7
    • 2142858450 scopus 로고
    • High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
    • Ohtani, T.; Kusumi, T.; Kashman, Y.; Kakisawa, H. High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids. J. Am. Chem. Soc. 1991, 113, 4092-4096.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 4092-4096
    • Ohtani, T.1    Kusumi, T.2    Kashman, Y.3    Kakisawa, H.4
  • 9
    • 0141452964 scopus 로고    scopus 로고
    • WinGX suite for small-molecule single-crystal crystallography
    • Farrugia, L. J. WinGX suite for small-molecule single-crystal crystallography. J. Appl. Crystallogr. 1999, 32, 837-838.
    • (1999) J. Appl. Crystallogr. , vol.32 , pp. 837-838
    • Farrugia, L.J.1
  • 10
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for windows version 1.07
    • Farrugia, L. J. ORTEP-3 for windows version 1.07. J. Appl. Crystallogr. 1997, 30, 565.
    • (1997) J. Appl. Crystallogr. , vol.30 , pp. 565
    • Farrugia, L.J.1
  • 12
    • 0027404651 scopus 로고
    • Cytotoxic and antimalarial bisbenzylisoquinolme alkaloids from Stephanla erecta
    • Likhitwitayawuid, K.; Angerhofer, C. K.; Cordell, G. A.; Pezzuto, J. M. Cytotoxic and antimalarial bisbenzylisoquinolme alkaloids from Stephanla erecta. J. Nat. Prod. 1993, 56, 30-38.
    • (1993) J. Nat. Prod. , vol.56 , pp. 30-38
    • Likhitwitayawuid, K.1    Angerhofer, C.K.2    Cordell, G.A.3    Pezzuto, J.M.4
  • 13
    • 0025367455 scopus 로고
    • Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines
    • Rubinstein, L. V.; Shoemaker, R. H.; Paull, K. D.; Simon, R. M.; Toslni, S.; Skehan, P.; Scudiero, D. A.; Monks, A.; Boyd, M. R. Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines. J. Natl. Cancer Inst. 1990, 52, 1113-1118.
    • (1990) J. Natl. Cancer Inst. , vol.52 , pp. 1113-1118
    • Rubinstein, L.V.1    Shoemaker, R.H.2    Paull, K.D.3    Simon, R.M.4    Toslni, S.5    Skehan, P.6    Scudiero, D.A.7    Monks, A.8    Boyd, M.R.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.