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Journal Abstract Search

101 related items for PubMed ID: 8273114

  • 1. Synthesis of 7- and 12-hydroxy- and 7,12-dihydroxy-3-keto-5 beta-cholan-24-oic acids by reduction of 3,7-, 3,12- and 3,7,12-oxo derivatives.
    Fantin G, Fogagnolo M, Medici A, Pedrini P, Cova U.
    Steroids; 1993 Nov; 58(11):524-6. PubMed ID: 8273114
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  • 2. Synthesis of 3 alpha,6 beta,7 alpha,12 beta- and 3 alpha,6 beta,7 beta,12 beta-tetrahydroxy-5 beta-cholanoic acids.
    Aggarwal SK, Batta AK, Salen G, Shefer S.
    Steroids; 1992 Mar; 57(3):107-11. PubMed ID: 1621264
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  • 3. Synthesis of potential cholelitholytic agents: 3 alpha,7 alpha,12 alpha-trihydroxy-7 beta-methyl-5 beta-cholanoic acid, 3 alpha,7 beta,12 alpha-trihydroxy-7 alpha-methyl-5 beta-cholanoic acid, and 3 alpha,12 alpha-dihydroxy-7 xi-methyl-5 beta-cholanoic acid.
    Kuroki S, Une M, Mosbach EH.
    J Lipid Res; 1985 Oct; 26(10):1205-11. PubMed ID: 4067415
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  • 4. Selective reduction of oxo bile acids: synthesis of 3 beta-, 7 beta-, and 12 beta-hydroxy bile acids.
    Batta AK, Aggarwal SK, Salen G, Shefer S.
    J Lipid Res; 1991 Jun; 32(6):977-83. PubMed ID: 1940629
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  • 5. Hydrogen-bonded aggregations of oxo-cholic acids.
    Bertolasi V, Ferretti V, Pretto L, Fantin G, Fogagnolo M, Bortolini O.
    Acta Crystallogr B; 2005 Jun; 61(Pt 3):346-56. PubMed ID: 15914900
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  • 8. Transformation of cholic acid by Arthrobacter simplex.
    Mukherjee E, Banerjee S, Mahato SB.
    Steroids; 1993 Oct; 58(10):484-90. PubMed ID: 8256259
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  • 10. Synthesis of 24-nor-5 beta-cholan-23-oic acid derivatives: a convenient and efficient one-carbon degradation of the side chain of natural bile acids.
    Schteingart CD, Hofmann AF.
    J Lipid Res; 1988 Oct; 29(10):1387-95. PubMed ID: 3235921
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  • 11. Determination of critical micellar concentrations of cholic acid and its keto derivatives.
    Posa M, Kevresan S, Mikov M, Cirin-Novta V, Sârbu C, Kuhajda K.
    Colloids Surf B Biointerfaces; 2007 Oct 01; 59(2):179-83. PubMed ID: 17604970
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  • 12. Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3 alpha,12 alpha,16 beta-trihydroxy-5 beta-cholan-24-oic acid).
    Nonappa, Maitra U.
    Steroids; 2010 Jul 01; 75(7):506-12. PubMed ID: 20359489
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  • 13. Biotransformation of bile acids by clostridia.
    Owen RW.
    J Med Microbiol; 1985 Oct 01; 20(2):233-8. PubMed ID: 2864454
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  • 16. 3-ketocholanoic acid is the major in vitro human hepatic microsomal metabolite of lithocholic acid.
    Deo AK, Bandiera SM.
    Drug Metab Dispos; 2009 Sep 01; 37(9):1938-47. PubMed ID: 19487251
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  • 17. Synthesis of 3alpha,7alpha,14alpha-trihydroxy-5beta-cholan-24-oic acid: a potential primary bile acid in vertebrates.
    Kakiyama G, Iida T, Goto T, Mano N, Goto J, Nambara T.
    Chem Pharm Bull (Tokyo); 2004 Mar 01; 52(3):371-4. PubMed ID: 14993766
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  • 18. Potential bile acid metabolites. 19. The epimeric 3 alpha,6,7 beta-trihydroxy- and 3 alpha,6,7 beta,12 alpha-tetrahydroxy-5 alpha-cholanoic acids.
    Iida T, Nishida S, Chang FC, Niwa T, Goto J, Nambara T.
    Steroids; 1993 Apr 01; 58(4):148-52. PubMed ID: 8493703
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  • 19. New bile acid analogs: 3 alpha, 7 alpha-dihydroxy-7 beta-methyl-5 beta-cholanoic acid, 3 alpha, 7 beta-dihydroxy-7 alpha-methyl-5 beta-cholanoic acid, and 3 alpha-hydroxy-7 xi-methyl-5 beta-cholanoic acid.
    Une M, Cohen BI, Mosbach EH.
    J Lipid Res; 1984 Apr 01; 25(4):407-10. PubMed ID: 6547159
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  • 20. A novel enzyme system for the reduction of 3-oxo bile acids in human red blood cells.
    Goto J, Miura H, Ando M, Yamato Y, Ikegawa S, Nambara T, Makino I.
    Steroids; 1996 Jul 01; 61(7):416-20. PubMed ID: 8837294
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