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Journal Abstract Search

110 related items for PubMed ID: 4045471

  • 1. Chemistry of acronycine. VIII. Selective synthesis of dimers and trimers of noracronycine and related compounds.
    Funayama S, Cordell GA.
    J Nat Prod; 1985; 48(4):536-46. PubMed ID: 4045471
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  • 5. Chemistry of acronycine, XI. Rearrangement of dihydronoracronycine to dihydroisonoracronycine-mechanistic studies.
    Funayama S, Cordell GA.
    J Nat Prod; 1985; 48(6):938-43. PubMed ID: 3841555
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  • 6. Acetylacroninium salts as soluble prodrugs of the antineoplastic agent acronine.
    Bourne DW, Higuchi T, Repta AJ.
    J Pharm Sci; 1977 May; 66(5):628-31. PubMed ID: 17711
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  • 7. Formation of a thio analog of noracronine.
    Dimmock JR, Repta AJ, Kaminski JJ.
    J Pharm Sci; 1979 Jan; 68(1):36-9. PubMed ID: 758461
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  • 8. [Synthesis and cytostatic action of 9-nitronoracronycine].
    Reisch J, Probst W.
    Arch Pharm (Weinheim); 1989 Jan; 322(1):31-4. PubMed ID: 2730287
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  • 9. Chemistry of acronycine IV. Minor constituents of acronine and the phytochemistry of the genus Acronychia.
    Funayama S, Cordell GA.
    J Nat Prod; 1984 Jan; 47(2):285-91. PubMed ID: 6736969
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  • 10. Chemistry of acronycine, VII. Facile rearrangement of dihydronoracronycine to dihydroisonoracronycine.
    Funayama S, Cordell GA.
    J Nat Prod; 1985 Jan; 48(1):114-7. PubMed ID: 3839256
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  • 11. Synthesis and cytotoxic activity of dimeric analogs of acronycine in the benzo[b]pyrano[3,2-h]acridin-7-one series.
    Gaslonde T, Michel S, Koch M, Pfeiffer B, Léonce S, Pierré A, Tillequin F.
    Chem Pharm Bull (Tokyo); 2007 May; 55(5):734-8. PubMed ID: 17473459
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  • 12. Chemistry of Acronycine: III.
    Funayama S, Cordell GA.
    Planta Med; 1983 Aug; 48(8):263-7. PubMed ID: 17404993
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  • 13. Synthesis and cytotoxic and antitumor activity of esters in the 1,2-dihydroxy-1,2-dihydroacronycine series.
    Elomri A, Mitaku S, Michel S, Skaltsounis AL, Tillequin F, Koch M, Pierré A, Guilbaud N, Léonce S, Kraus-Berthier L, Rolland Y, Atassi G.
    J Med Chem; 1996 Nov 22; 39(24):4762-6. PubMed ID: 8941390
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  • 14. Synthesis and cytotoxic activity of acronycine analogues in the benzo[c]pyrano[3,2-h]acridin-7-one and naphtho[1,2-b][1,7] and [1,10]-phenanthrolin-7(14H)-one series.
    Bongui JB, Elomri A, Cahard D, Tillequin F, Pfeiffer B, Pierré A, Seguin E.
    Chem Pharm Bull (Tokyo); 2005 Dec 22; 53(12):1540-6. PubMed ID: 16327185
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  • 16. Synthesis and cytotoxic activity of 11-nitro and 11-amino derivatives of acronycine and 6-demethoxyacronycine.
    Elomri A, Michel S, Koch M, Seguin E, Tillequin F, Pierré A, Atassi G.
    Chem Pharm Bull (Tokyo); 1999 Nov 22; 47(11):1604-6. PubMed ID: 10605058
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  • 18. Structure-activity relationships in the acronycine and benzo[b]acronycine series: role of the pyran ring.
    Do Q, Thi Mai HD, Gaslonde T, Pfeiffer B, Léonce S, Pierré A, Michel S, Tillequin F, Dufat H.
    Eur J Med Chem; 2008 Dec 22; 43(12):2677-87. PubMed ID: 18342404
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  • 19. Synthesis and cytotoxic activity of benzo[a]acronycine and benzo[b]acronycine substituted on the A ring.
    Gaslonde T, Covello F, Velazquez-Alonso L, Léonce S, Pierré A, Pfeiffer B, Michel S, Tillequin F.
    Eur J Med Chem; 2011 May 22; 46(5):1861-73. PubMed ID: 21411193
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  • 20. Synthesis and cytotoxic activity of acronycine derivatives modified at the pyran ring.
    Elomri A, Skaltsounis AL, Michel S, Tillequin F, Koch M, Rolland Y, Pierré A, Atassi G.
    Chem Pharm Bull (Tokyo); 1996 Nov 22; 44(11):2165-8. PubMed ID: 8945782
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