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Journal Abstract Search

184 related items for PubMed ID: 16365835

  • 1. Sphingolactones: selective and irreversible inhibitors of neutral sphingomyelinase.
    Wascholowski V, Giannis A.
    Angew Chem Int Ed Engl; 2006 Jan 23; 45(5):827-30. PubMed ID: 16365835
    [No Abstract] [Full Text] [Related]

  • 2. Synthesis and evaluation of novel phosphate ester analogs as neutral sphingomyelinase inhibitors.
    Imagawa H, Oda M, Takemoto T, Yamauchi R, Yoshikawa T, Yamamoto H, Nishizawa M, Takahashi H, Hashimoto M, Yabiku K, Nagahama M, Sakurai J.
    Bioorg Med Chem Lett; 2010 Jul 01; 20(13):3868-71. PubMed ID: 20627555
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  • 3. Synthesis of a nitrogen analogue of sphingomyelin as a sphingomyelinase inhibitor.
    Hakogi T, Taichi M, Katsumura S.
    Org Lett; 2003 Aug 07; 5(16):2801-4. PubMed ID: 12889878
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  • 4. Biological evaluation of sphingomyelin analogues as inhibitors of sphingomyelinase.
    Taguchi M, Goda K, Sugimoto K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T.
    Bioorg Med Chem Lett; 2003 Nov 03; 13(21):3681-4. PubMed ID: 14552757
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  • 5. Development of carbohydrate-derived inhibitors of acid sphingomyelinase.
    Roth AG, Redmer S, Arenz C.
    Bioorg Med Chem; 2010 Jan 15; 18(2):939-44. PubMed ID: 20005726
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  • 6. Identification and evaluation of neutral sphingomyelinase 2 inhibitors.
    Lee DH, Kim SH, Ahn KH, Kim SK, Choi JM, Ji JE, Won JH, Park YH, Lim C, Kim S, Kim DK.
    Arch Pharm Res; 2011 Feb 15; 34(2):229-36. PubMed ID: 21380806
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  • 9. Synthesis and preliminary evaluation of a modified estradiol-core bearing a fused γ-lactone as non-estrogenic inhibitor of 17β-hydroxysteroid dehydrogenase type 1.
    Ouellet E, Ayan D, Poirier D.
    Bioorg Med Chem Lett; 2011 Sep 15; 21(18):5510-3. PubMed ID: 21782424
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  • 10. Potent inhibition of acid sphingomyelinase by phosphoinositide analogues.
    Roth AG, Redmer S, Arenz C.
    Chembiochem; 2009 Sep 21; 10(14):2367-74. PubMed ID: 19688786
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  • 12. Synthesis of non-competitive inhibitors of sphingomyelinases with significant activity.
    Yokomatsu T, Murano T, Akiyama T, Koizumi J, Shibuya S, Tsuji Y, Soeda S, Shimeno H.
    Bioorg Med Chem Lett; 2003 Jan 20; 13(2):229-36. PubMed ID: 12482429
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  • 13. Synthesis of sphingomyelin sulfur analogue and its behavior toward sphingomyelinase.
    Hakogi T, Fujii S, Morita M, Ikeda K, Katsumura S.
    Bioorg Med Chem Lett; 2005 Apr 15; 15(8):2141-4. PubMed ID: 15808485
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  • 14. Synthesis and biological activity of a novel inhibitor of dihydroceramide desaturase.
    Munoz-Olaya JM, Matabosch X, Bedia C, Egido-Gabás M, Casas J, Llebaria A, Delgado A, Fabriàs G.
    ChemMedChem; 2008 Jun 15; 3(6):946-53. PubMed ID: 18236489
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  • 15. Total synthesis of lactacystin and salinosporamide A.
    Shibasaki M, Kanai M, Fukuda N.
    Chem Asian J; 2007 Jan 08; 2(1):20-38. PubMed ID: 17441136
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  • 16. Sphingomyelin analogues as inhibitors of sphingomyelinase.
    Taguchi M, Sugimoto K, Goda K, Akama T, Yamamoto K, Suzuki T, Tomishima Y, Nishiguchi M, Arai K, Takahashi K, Kobori T.
    Bioorg Med Chem Lett; 2003 Jun 16; 13(12):1963-6. PubMed ID: 12781174
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  • 17. Synthesis of sphingomyelin carbon analogues as sphingomyelinase inhibitors.
    Hakogi T, Monden Y, Taichi M, Iwama S, Fujii S, Ikeda K, Katsumura S.
    J Org Chem; 2002 Jul 12; 67(14):4839-46. PubMed ID: 12098296
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  • 19. Sesquiterpene lactones are potent and irreversible inhibitors of the antibacterial target enzyme MurA.
    Bachelier A, Mayer R, Klein CD.
    Bioorg Med Chem Lett; 2006 Nov 01; 16(21):5605-9. PubMed ID: 16945528
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  • 20. Concise asymmetric total synthesis of scyphostatin, a potent inhibitor of neutral sphingomyelinase.
    Fujioka H, Sawama Y, Kotoku N, Ohnaka T, Okitsu T, Murata N, Kubo O, Li R, Kita Y.
    Chemistry; 2007 Nov 01; 13(36):10225-38. PubMed ID: 17907134
    [Abstract] [Full Text] [Related]

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