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Journal Abstract Search

116 related items for PubMed ID: 1486654

  • 1.
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  • 2. Inhibitors of sterol synthesis. An improved chemical synthesis of 26-oxygenated delta 8(14)-15-ketosterols having the 25R configuration.
    Siddiqui AU, Wilson WK, Schroepfer GJ.
    Chem Phys Lipids; 1994 May 23; 71(2):205-18. PubMed ID: 8076403
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  • 3. Assigning stereodiversity of the 27-Me group of furostane-type steroidal saponins via NMR chemical shifts.
    Agrawal PK.
    Steroids; 2005 Sep 23; 70(10):715-24. PubMed ID: 15923015
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  • 6. Inhibitors of sterol synthesis. Tritium-labeled 26-hydroxycholesterol of high specific activity from a byproduct of the Clemmensen reduction of diosgenin.
    Ni Y, Kisic A, Wilson WK, Schroepfer GJ.
    J Lipid Res; 1994 Mar 23; 35(3):546-59. PubMed ID: 8014589
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  • 7. Analysis of unsaturated C27 sterols by nuclear magnetic resonance spectroscopy.
    Wilson WK, Sumpter RM, Warren JJ, Rogers PS, Ruan B, Schroepfer GJ.
    J Lipid Res; 1996 Jul 23; 37(7):1529-55. PubMed ID: 8827525
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  • 9. Inhibitors of sterol synthesis. Synthesis and spectral properties of 3 beta-hydroxy-25,26,26,26,27,27,27-heptafluoro-5 alpha-cholestan-15-one.
    Siddiqui AU, Swaminathan S, Su X, Wilson WK, Schroepfer GJ.
    Chem Phys Lipids; 1997 Apr 25; 86(2):95-119. PubMed ID: 9179993
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  • 11. Steroids from Harrisonia abyssinica.
    Baldé AM, Apers S, De Bruyne TE, Van den Heuvel H, Claeys M, Vlietinck AJ, Pieters LA.
    Planta Med; 2000 Feb 25; 66(1):67-9. PubMed ID: 10705738
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  • 12. Protein expression, selective isotopic labeling, and analysis of hyperfine-shifted NMR signals of Anabaena 7120 vegetative [2Fe-2S]ferredoxin.
    Cheng H, Westler WM, Xia B, Oh BH, Markley JL.
    Arch Biochem Biophys; 1995 Jan 10; 316(1):619-34. PubMed ID: 7840674
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  • 14. Quaternary Alkylammonium Conjugates of Steroids: Synthesis, Molecular Structure, and Biological Studies.
    Brycki B, Koenig H, Pospieszny T.
    Molecules; 2015 Nov 23; 20(11):20887-900. PubMed ID: 26610455
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  • 16. Synthesis of side-chain oxysterols and their enantiomers through cross-metathesis reactions of Δ22 steroids.
    Brownholland DP, Covey DF.
    Steroids; 2017 May 23; 121():22-31. PubMed ID: 28300584
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  • 17. 1H HR/MAS NMR in the suspended state: molecular recognition processes in liquid chromatography between steroids and a silica hydride-based cholesterol phase.
    Friebolin V, Bayer MP, Matyska MT, Pesek JJ, Albert K.
    J Sep Sci; 2009 May 23; 32(10):1722-8. PubMed ID: 19391175
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  • 18. 1H,13C, 19F NMR, and ESI mass spectral characterization of two geminal difluorosteroids.
    Sievänen E, Noponen V, Král V, Bríza T, Kolehmainen E.
    Magn Reson Chem; 2008 Apr 23; 46(4):392-7. PubMed ID: 18273878
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  • 19. Three new steroidal saponins from Fritillaria pallidiflora.
    Shen S, Chen CJ, Bu R, Ga L, Li GY, Tan Y, Li X, Wang JH.
    J Asian Nat Prod Res; 2011 Oct 23; 13(11):1014-22. PubMed ID: 22008065
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  • 20. Steroidal glycosides from the underground parts of Helleborus caucasicus.
    Bassarello C, Muzashvili T, Skhirtladze A, Kemertelidze E, Pizza C, Piacente S.
    Phytochemistry; 2008 Mar 23; 69(5):1227-33. PubMed ID: 18226823
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