BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 15467275)

  • 1. [Systematic synthesis of antitumor annonaceous acetogenins].
    Kojima N
    Yakugaku Zasshi; 2004 Oct; 124(10):673-81. PubMed ID: 15467275
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Systematic synthesis of Bis-THF ring cores in annonaceous acetogenins.
    Maezaki N; Kojima N; Tominaga H; Yanai M; Tanaka T
    Org Lett; 2003 May; 5(9):1411-4. PubMed ID: 12713286
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A bidirectional approach to the synthesis of a complete library of adjacent-bis-THF annonaceous acetogenins.
    Das S; Li LS; Abraham S; Chen Z; Sinha SC
    J Org Chem; 2005 Jul; 70(15):5922-31. PubMed ID: 16018687
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Highly stereoselective and stereodivergent synthesis of four types of THF cores in acetogenins using a C4-chiral building block.
    Maezaki N; Kojima N; Asai M; Tominaga H; Tanaka T
    Org Lett; 2002 Aug; 4(17):2977-80. PubMed ID: 12182603
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vitro antitumor structure-activity relationships of threo/trans/threo/trans/erythro bis-tetrahydrofuranic acetogenins: correlations with their inhibition of mitochondrial complex I.
    Tormo JR; DePedro N; Royo I; Barrachina I; Zafra-Polo MC; Cuadrillero C; Hernández P; Cortes D; Peláez F
    Oncol Res; 2005; 15(3):129-38. PubMed ID: 16050134
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New strategy for the construction of a monotetrahydrofuran ring in Annonaceous acetogenin based on a ruthenium ring-closing metathesis: application to the synthesis of Solamin.
    Prestat G; Baylon C; Heck MP; Grasa GA; Nolan SP; Mioskowski C
    J Org Chem; 2004 Aug; 69(17):5770-3. PubMed ID: 15307756
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Annonaceous acetogenins: the hydroxyl groups and THF rings are crucial structural elements for targeting the mitochondria, demonstration with the synthesis of fluorescent squamocin analogues.
    Derbré S; Roué G; Poupon E; Susin SA; Hocquemiller R
    Chembiochem; 2005 Jun; 6(6):979-82. PubMed ID: 15861433
    [No Abstract]   [Full Text] [Related]  

  • 8. Stereochemically general approach to adjacent bis(tetrahydrofuran) cores of annonaceous acetogenins.
    Wysocki LM; Dodge MW; Voight EA; Burke SD
    Org Lett; 2006 Nov; 8(24):5637-40. PubMed ID: 17107091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An outside-in approach to adjacent bistetrahydrofuran annonaceous acetogenins with C2 core symmetry. Total synthesis of asimicin and a C32 analogue.
    Marshall JA; Sabatini JJ
    Org Lett; 2006 Aug; 8(16):3557-60. PubMed ID: 16869659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Total synthesis of (+)-muconin.
    Yoshimitsu T; Makino T; Nagaoka H
    J Org Chem; 2004 Mar; 69(6):1993-8. PubMed ID: 15058945
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stereodivergent and reiterative synthesis of bistetrahydrofuran ring cores of annonaceous acetogenins.
    Kojima N; Maezaki N; Tominaga H; Yanai M; Urabe D; Tanaka T
    Chemistry; 2004 Feb; 10(3):672-80. PubMed ID: 14767931
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Annojahnin from Annona jahnii: a possible precursor of mono-tetrahydrofuran acetogenins.
    Colman-Saizarbitoria T; Johnson HA; Alali FQ; Hopp DC; Rogers LL; McLaughlin JL
    Phytochemistry; 1998 Nov; 49(6):1609-16. PubMed ID: 9862137
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Synthesis of the proposed structure of mucoxin via regio- and stereoselective tetrahydrofuran ring-forming strategies.
    Narayan RS; Borhan B
    J Org Chem; 2006 Feb; 71(4):1416-29. PubMed ID: 16468789
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sequencing of three-component olefin metatheses: total synthesis of either (+)-gigantecin or (+)-14-deoxy-9-oxygigantecin.
    Hoye TR; Eklov BM; Jeon J; Khoroosi M
    Org Lett; 2006 Jul; 8(15):3383-6. PubMed ID: 16836411
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Synthesis of pyragonicin.
    Strand D; Rein T
    Org Lett; 2005 Jun; 7(13):2779-81. PubMed ID: 15957945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Induction of cell death of gastric cancer cells by a modified compound of the annonaceous acetogenin family.
    Huang GR; Jiang S; Wu YL; Jin Y; Yao ZJ; Wu JR
    Chembiochem; 2003 Nov; 4(11):1216-21. PubMed ID: 14613114
    [TBL] [Abstract][Full Text] [Related]  

  • 17. In vitro antitumor activities of new synthetic bistetrahydrofuran derivatives as analogs of Annonaceous acetogenins.
    Sasaki S; Maruta K; Naito H; Maemura R; Kawahara E; Maeda M
    Chem Pharm Bull (Tokyo); 1998 Jan; 46(1):154-8. PubMed ID: 9468648
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Total synthesis of the proposed structure for pyragonicin.
    Takahashi S; Ogawa N; Koshino H; Nakata T
    Org Lett; 2005 Jun; 7(13):2783-6. PubMed ID: 15957946
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ABC synthesis and antitumor activity of a series of Annonaceous acetogenin analogs with a threo, trans, threo, trans, threo-bis-tetrahydrofuran core unit.
    Marshall JA; Sabatini JJ; Valeriote F
    Bioorg Med Chem Lett; 2007 May; 17(9):2434-7. PubMed ID: 17329102
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biogenetic relationships between Annonaceous acetogenins: squamocin is not a precursor of chamuvarinin based on a semisynthetic study.
    Derbré S; Poupon E; Gleye C; Hocquemiller R
    J Nat Prod; 2007 Feb; 70(2):300-3. PubMed ID: 17279796
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.