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154 related items for PubMed ID: 6520115

  • 1. Stereospecific formation of (24E)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholest-24-en-26-oic acid and (24R,25S)-3 alpha,7 alpha,12 alpha,24-tetrahydroxy-5 beta-cholestan-26-oic acid from either (25R)- or (25S)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid by rat liver homogenate.
    Une M, Morigami I, Kihira K, Hoshita T.
    J Biochem; 1984 Oct; 96(4):1103-7. PubMed ID: 6520115
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  • 4. Stereochemistry of intermediates in the conversion of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acid to cholic acid by rat liver peroxisomes.
    Une M, Izumi N, Hoshita T.
    J Biochem; 1993 Feb; 113(2):141-3. PubMed ID: 8468319
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  • 5. Identification of (24E)-3 alpha,7 alpha-dihydroxy-5 beta-cholest-24-enoic acid and (24R,25S)-3 alpha,7 alpha,24-trihydroxy-5 beta-cholestanoic acid as intermediates in the conversion of 3 alpha,7 alpha-dihydroxy-5 beta-cholestanoic acid to chenodeoxycholic acid in rat liver homogenates.
    Une M, Inoue A, Kurosawa T, Tohma M, Hoshita T.
    J Lipid Res; 1994 Apr; 35(4):620-4. PubMed ID: 8006516
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  • 6. Biliary bile acids in birds of the Cotingidae family: taurine-conjugated (24R,25R)-3α,7α,24-trihydroxy-5β-cholestan-27-oic acid and two epimers (25R and 25S) of 3α,7α-dihydroxy-5β-cholestan-27-oic acid.
    Hagey LR, Iida T, Ogawa S, Adachi Y, Une M, Mushiake K, Maekawa M, Shimada M, Mano N, Hofmann AF.
    Steroids; 2011 Apr; 76(10-11):1126-35. PubMed ID: 21600907
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  • 7. Substrate stereospecificity in oxidation of (25S)-3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoyl-CoA by peroxisomal trihydroxy-5 beta-cholestanoyl-CoA oxidase.
    Pedersen JI, Veggan T, Björkhem I.
    Biochem Biophys Res Commun; 1996 Jul 05; 224(1):37-42. PubMed ID: 8694830
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  • 8. Synthesis of 3 alpha, 7 alpha-dihydroxy-5 beta-cholestan-26-oic acid from 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid: configuration in the bile of Alligator mississippiensis.
    Batta AK, Mirchandani R, Salen G, Shefer S.
    Steroids; 1992 Apr 05; 57(4):162-6. PubMed ID: 1519259
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  • 9. Synthesis of diastereomers of 3 alpha,7 alpha,12 alpha, 24-tetrahydroxy- and 3 alpha,7 alpha,24-trihydroxy-5 beta-cholestan- 26-oic acids and their structures.
    Kurosawa T, Sato M, Nakano H, Tohma M.
    Steroids; 1996 Jul 05; 61(7):421-8. PubMed ID: 8837295
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  • 10. Stereoisomeric inversion of (25R)- and (25S)-3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestanoic acids in rat liver peroxisome.
    Ikegawa S, Goto T, Watanabe H, Goto J.
    Biol Pharm Bull; 1995 Jul 05; 18(7):1027-9. PubMed ID: 7581245
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  • 11. Synthesis of 3 alpha, 7 alpha, 12 alpha-trihydroxy- and 3 alpha, 7 alpha-dihydroxy-5 beta-cholestan-26-oic acids by the use of beta-ketosulfoxide.
    Kurosawa T, Nakano H, Sato M, Tohma M.
    Steroids; 1995 Jul 05; 60(7):439-44. PubMed ID: 7482627
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  • 12. Formation of varanic acid, 3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxy-5 beta-cholestanoic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid in Bombina orientalis.
    Une M, Inoue A, Hoshita T.
    Steroids; 1996 Nov 05; 61(11):639-41. PubMed ID: 8916357
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  • 13. Synthesis of four diastereoisomers at carbons 24 and 25 of 3 alpha,7 alpha,12 alpha,24-tetrahydroxy-5 beta-cholestan-26-oic acid, intermediates of bile acid biosynthesis.
    Une M, Nagai F, Kihira K, Kuramoto T, Hoshita T.
    J Lipid Res; 1983 Jul 05; 24(7):924-9. PubMed ID: 6631226
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  • 14. Bile acids and bile alcohols of bullfrog.
    Noma Y, Une M, Kihira K, Yasuda M, Kuramoto T, Hoshita T.
    J Lipid Res; 1980 Mar 05; 21(3):339-46. PubMed ID: 6966672
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  • 15. The minor bile acids of the toad, Bufo vulgaris formosus.
    Une M, Kuramoto T, Hoshita T.
    J Lipid Res; 1983 Nov 05; 24(11):1468-74. PubMed ID: 6655364
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  • 16. Biosynthesis of cholic acid in rat liver: formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy- and 3 alpha, 7 alpha, 12 alpha, 24-tetrahydroxy-5 beta-cholestanoic acids.
    Gustafsson J.
    Lipids; 1980 Feb 05; 15(2):113-21. PubMed ID: 7374359
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  • 17. Chemical synthesis of the (25R)- and (25S)-epimers of 3α,7α,12α-trihydroxy-5α-cholestan-27-oic acid as well as their corresponding glycine and taurine conjugates.
    Ogawa S, Mitamura K, Ikegawa S, Krasowski MD, Hagey LR, Hofmann AF, Iida T.
    Chem Phys Lipids; 2011 Jul 05; 164(5):368-77. PubMed ID: 21554864
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  • 18. Cleavage of the taurine conjugate of 3 alpha,7 alpha,12 alpha-trihydroxy-5 beta-cholestan-26-oic acid by rat fecal bacteria.
    Batta AK, Salen G, Cheng FW, Shefer S.
    J Biol Chem; 1979 Dec 10; 254(23):11907-9. PubMed ID: 500682
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  • 19. Effect of the hydroxyl group on the oxidative cleavage (beta-oxidation) of steroidal side chain for bile acid biosynthesis in rat liver homogenate.
    Kurosawa T, Sato M, Kikuchi F, Watanabe T, Suga T, Tohma M.
    Steroids; 1997 Jun 10; 62(6):474-81. PubMed ID: 9185295
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  • 20. Bile salts of the toad, Bufo marinus: characterization of a new unsaturated higher bile acid, 3 alpha,7 alpha,12 alpha,26-tetrahydroxy-5 beta-cholest-23-en-27-oic acid.
    Yoshii M, Une M, Kihira K, Kuramoto T, Akizawa T, Yoshioka M, Butler VP, Hoshita T.
    J Lipid Res; 1994 Sep 10; 35(9):1646-51. PubMed ID: 7806978
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