BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 20371180)

  • 21. Cytotoxic triterpenoids from the leaves of Euphorbia pulcherrima.
    Smith-Kielland I; Dornish JM; Malterud KE; Hvistendahl G; Rømming C; Bøckman OC; Kolsaker P; Stenstrøm Y; Nordal A
    Planta Med; 1996 Aug; 62(4):322-5. PubMed ID: 8792663
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 2-Thienyl-4-furyl-6-aryl pyridine derivatives: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study.
    Thapa P; Karki R; Thapa U; Jahng Y; Jung MJ; Nam JM; Na Y; Kwon Y; Lee ES
    Bioorg Med Chem; 2010 Jan; 18(1):377-86. PubMed ID: 19939682
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Dimethoxybenzo[i]phenanthridine-12-carboxylic acid derivatives and 6H-dibenzo[c,h][2,6]naphthyridin-5-ones with potent topoisomerase I-targeting activity and cytotoxicity.
    Ruchelman AL; Zhu S; Zhou N; Liu A; Liu LF; LaVoie EJ
    Bioorg Med Chem Lett; 2004 Nov; 14(22):5585-9. PubMed ID: 15482929
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Bioactivity-guided isolation of cytotoxic triterpenoids from the trunk of Berberis koreana.
    Kim KH; Choi SU; Lee KR
    Bioorg Med Chem Lett; 2010 Mar; 20(6):1944-7. PubMed ID: 20176479
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Two new triterpenoid saponins cytotoxic to human glioblastoma U251MG cells from Ardisia pusilla.
    Tang HF; Yun J; Lin HW; Chen XL; Wang XJ; Cheng G
    Chem Biodivers; 2009 Sep; 6(9):1443-52. PubMed ID: 19774606
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cytotoxic compounds from Annonaceus species as DNA topoisomerase I poisons.
    López-Lázaro M; Martín-Cordero C; Bermejo A; Cortes D; Ayuso MJ
    Anticancer Res; 2001; 21(5):3493-7. PubMed ID: 11848514
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Design, synthesis, and biological evaluation of cytotoxic 11-alkenylindenoisoquinoline topoisomerase I inhibitors and indenoisoquinoline-camptothecin hybrids.
    Fox BM; Xiao X; Antony S; Kohlhagen G; Pommier Y; Staker BL; Stewart L; Cushman M
    J Med Chem; 2003 Jul; 46(15):3275-82. PubMed ID: 12852757
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Effect of E-ring modifications in camptothecin on topoisomerase I inhibition: a quantum mechanics treatment.
    Xiao X; Cushman M
    J Org Chem; 2005 Nov; 70(23):9584-7. PubMed ID: 16268636
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Peniciside, a new triterpenoid glycoside, from the fungus Penicillium sp. 169.
    Yuan XH; Xu GB; Wu WL; Yang T; Li GY
    Arch Pharm Res; 2012 Feb; 35(2):311-4. PubMed ID: 22370784
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cytotoxic oxygenated triterpenoid saponins from Symplocos chinensis.
    Fu G; Liu Y; Yu S; Huang X; Hu Y; Chen X; Zhang F
    J Nat Prod; 2006 Dec; 69(12):1680-6. PubMed ID: 17190442
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Substitution at the F-ring N-imide of the indolocarbazole antitumor drug NB-506 increases the cytotoxicity, DNA binding, and topoisomerase I inhibition activities.
    Bailly C; Qu X; Chaires JB; Colson P; Houssier C; Ohkubo M; Nishimura S; Yoshinari T
    J Med Chem; 1999 Jul; 42(15):2927-35. PubMed ID: 10425102
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cytotoxic chemical constituents from the roots of Cimicifuga foetida. [corrected].
    Nian Y; Zhang YL; Chen JC; Lu L; Qiu MH; Qing C
    J Nat Prod; 2010 Feb; 73(2):93-8. PubMed ID: 20121210
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cytotoxic triterpenoid glycosides from the roots of Gordonia chrysandra.
    Yu L; Yang JZ; Chen XG; Shi JG; Zhang DM
    J Nat Prod; 2009 May; 72(5):866-70. PubMed ID: 20560647
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cytotoxic triterpenoids from the rhizomes of Astilbe chinensis.
    Cai XF; Park BY; Ahn KS; Kwon OK; Lee HK; Oh SR
    J Nat Prod; 2009 Jul; 72(7):1241-4. PubMed ID: 19585998
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Synthesis, cytotoxic activities and structure-activity relationships of topoisomerase I inhibitors: indolizinoquinoline-5,12-dione derivatives.
    Cheng Y; An LK; Wu N; Wang XD; Bu XZ; Huang ZS; Gu LQ
    Bioorg Med Chem; 2008 Apr; 16(8):4617-25. PubMed ID: 18296054
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Characterization of a novel topoisomerase I mutation from a camptothecin-resistant human prostate cancer cell line.
    Urasaki Y; Laco GS; Pourquier P; Takebayashi Y; Kohlhagen G; Gioffre C; Zhang H; Chatterjee D; Pantazis P; Pommier Y
    Cancer Res; 2001 Mar; 61(5):1964-9. PubMed ID: 11280753
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Differential expression of topoisomerase I and RAD52 protein in yeast reveals new facets of the mechanism of action of bisdioxopiperazine compounds.
    van Hille B; Clerc X; Creighton AM; Hill BT
    Br J Cancer; 1999 Nov; 81(5):800-7. PubMed ID: 10555749
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Synthesis and cytotoxic activity of a new series of topoisomerase I inhibitors.
    Dallavalle S; Gattinoni S; Mazzini S; Scaglioni L; Merlini L; Tinelli S; Beretta GL; Zunino F
    Bioorg Med Chem Lett; 2008 Feb; 18(4):1484-9. PubMed ID: 18248813
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Antitumor agents. 180. Chemical Studies and cytotoxic evaluation of cumingianosides and cumindysoside A, antileukemic triterpene glucosides with a 14,18-cycloapotirucallane skeleton.
    Kashiwada Y; Fujioka T; Mihashi K; Chen IS; Katayama H; Ikeshiro Y; Lee KH
    J Nat Prod; 1997 Nov; 60(11):1105-14. PubMed ID: 9392879
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 2,6-Dithienyl-4-furyl pyridines: Synthesis, topoisomerase I and II inhibition, cytotoxicity, structure-activity relationship, and docking study.
    Basnet A; Thapa P; Karki R; Choi H; Choi JH; Yun M; Jeong BS; Jahng Y; Na Y; Cho WJ; Kwon Y; Lee CS; Lee ES
    Bioorg Med Chem Lett; 2010 Jan; 20(1):42-7. PubMed ID: 19954977
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.