BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 25247616)

  • 1. General strategy for synthesis of C-19 methyl-substituted sarpagine/macroline/ajmaline indole alkaloids including total synthesis of 19(S),20(R)-dihydroperaksine, 19(S),20(R)-dihydroperaksine-17-al, and peraksine.
    Edwankar RV; Edwankar CR; Deschamps JR; Cook JM
    J Org Chem; 2014 Nov; 79(21):10030-48. PubMed ID: 25247616
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Regiospecific, enantiospecific total synthesis of C-19 methyl substituted sarpagine alkaloids dihydroperaksine-17-al and dihydroperaksine.
    Edwankar RV; Edwankar CR; Deschamps J; Cook JM
    Org Lett; 2011 Oct; 13(19):5216-9. PubMed ID: 21877687
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Total Synthesis of Sarpagine-Related Bioactive Indole Alkaloids.
    Rahman MT; Deschamps JR; Imler GH; Cook JM
    Chemistry; 2018 Feb; 24(10):2354-2359. PubMed ID: 29244896
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sarpagine and Related Alkaloids.
    Namjoshi OA; Cook JM
    Alkaloids Chem Biol; 2016; 76():63-169. PubMed ID: 26827883
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Enantiospecific total synthesis of (-)-(E)16-epiaffinisine, (+)-(E)16-epinormacusine B, and (+)-dehydro-16-epiaffinisine as well as the stereocontrolled total synthesis of alkaloid G.
    Yu J; Wang T; Wearing XZ; Ma J; Cook JM
    J Org Chem; 2003 Jul; 68(15):5852-9. PubMed ID: 12868917
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An improved total synthesis of (+)-macroline and alstonerine as well as the formal total synthesis of (-)-talcarpine and (-)-anhydromacrosalhine-methine.
    Liao X; Zhou H; Yu J; Cook JM
    J Org Chem; 2006 Nov; 71(23):8884-90. PubMed ID: 17081019
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Discovery of Unusual Ajmaline-Macroline Type Bisindole Alkaloids from Alstonia macrophylla by Building Blocks-Based Molecular Networking.
    Li ZW; Fan CL; Sun B; Huang L; Wang ZQ; Huang XJ; Zhang SQ; Ye WC; Wu ZL; Zhang XQ
    Chemistry; 2024 Feb; 30(8):e202303519. PubMed ID: 38018776
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bisindole Alkaloids from the
    Pandey KP; Rahman MT; Cook JM
    Molecules; 2021 Jun; 26(11):. PubMed ID: 34200196
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of Bisindole Alkaloids from the Apocynaceae Which Contain a Macroline or Sarpagine Unit: A Review.
    Rahman MT; Tiruveedhula VV; Cook JM
    Molecules; 2016 Nov; 21(11):. PubMed ID: 27854259
    [TBL] [Abstract][Full Text] [Related]  

  • 10. General approach for the synthesis of sarpagine/macroline indole alkaloids. Enantiospecific total synthesis of the indole alkaloid trinervine.
    Liu X; Cook JM
    Org Lett; 2001 Dec; 3(25):4023-6. PubMed ID: 11735575
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structure units oriented approach towards collective synthesis of sarpagine-ajmaline-koumine type alkaloids.
    Chen W; Ma Y; He W; Wu Y; Huang Y; Zhang Y; Tian H; Wei K; Yang X; Zhang H
    Nat Commun; 2022 Feb; 13(1):908. PubMed ID: 35177620
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Macroline, akuammiline, sarpagine, and ajmaline alkaloids from Alstonia macrophylla.
    Lim SH; Low YY; Sinniah SK; Yong KT; Sim KS; Kam TS
    Phytochemistry; 2014 Feb; 98():204-15. PubMed ID: 24342109
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The ajmaline group of indole alkaloids.
    Lounasmaa M; Hanhinen P
    Alkaloids Chem Biol; 2001; 55():1-87. PubMed ID: 11704984
    [No Abstract]   [Full Text] [Related]  

  • 14. Completion of the Total Synthesis of Several Bioactive Sarpagine/Macroline Alkaloids including the Important NF-κB Inhibitor
    Rahman MT; Tiruveedhula VVNPB; Stephen MR; Rallapalli SK; Pandey KP; Cook JM
    Molecules; 2022 Mar; 27(5):. PubMed ID: 35268836
    [TBL] [Abstract][Full Text] [Related]  

  • 15. General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine.
    Wang T; Cook JM
    Org Lett; 2000 Jul; 2(14):2057-9. PubMed ID: 10891229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New alkaloids of the sarpagine group from Rauvolfia serpentina hairy root culture.
    Sheludko Y; Gerasimenko I; Kolshorn H; Stöckigt J
    J Nat Prod; 2002 Jul; 65(7):1006-10. PubMed ID: 12141861
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The enantiospecific, stereospecific total synthesis of the ring-A oxygenated sarpagine indole alkaloids (+)-majvinine, (+)-10-methoxyaffinisine, and (+)-N(a)-methylsarpagine, as well as the total synthesis of the alstonia bisindole alkaloid macralstonidine.
    Zhao S; Liao X; Wang T; Flippen-Anderson J; Cook JM
    J Org Chem; 2003 Aug; 68(16):6279-95. PubMed ID: 12895062
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lumutinines A-D, linearly fused macroline-macroline and macroline-sarpagine bisindoles from Alstonia macrophylla.
    Lim SH; Tan SJ; Low YY; Kam TS
    J Nat Prod; 2011 Dec; 74(12):2556-62. PubMed ID: 22148233
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Enantiospecific total synthesis of the important biogenetic intermediates along the ajmaline pathway, (+)-polyneuridine and (+)-polyneuridine aldehyde, as well as 16-epivellosimine and macusine A.
    Yin W; Kabir MS; Wang Z; Rallapalli SK; Ma J; Cook JM
    J Org Chem; 2010 May; 75(10):3339-49. PubMed ID: 20392128
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A general strategy for the synthesis of vincamajine-related indole alkaloids: stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy-17-epivincamajine as well as the related quebrachidine diol, vincamajine diol, and vincarinol.
    Yu J; Wearing XZ; Cook JM
    J Org Chem; 2005 May; 70(10):3963-79. PubMed ID: 15876085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.