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PUBMED FOR HANDHELDS

Journal Abstract Search


167 related items for PubMed ID: 3235921

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Microbial transformation of bile acids. A unified scheme for bile acid degradation, and hydroxylation of bile acids.
    Hayakawa S.
    Z Allg Mikrobiol; 1982 Oct; 22(5):309-26. PubMed ID: 7123999
    [Abstract] [Full Text] [Related]

  • 3. Novel derivatives of 3 alpha,7 alpha-dihydroxy-5 beta-cholan-24-oic acid (chenodeoxycholic acid) and 3 alpha,7 beta-dihydroxy-5 beta-cholan-24-oic acid (ursodeoxycholic acid).
    Kritchevsky D, Poli G, Scolastico C, Sirtori CR.
    Steroids; 1986 Jan; 47(1):41-8. PubMed ID: 3810698
    [Abstract] [Full Text] [Related]

  • 4. 5 beta-hydroxylation by the liver. Identification of 3,5,7-trihydroxy nor-bile acids as new major biotransformation products of 3,7-dihydroxy nor-bile acids in rodents.
    Schteingart CD, Hagey LR, Setchell KD, Hofmann AF.
    J Biol Chem; 1993 May 25; 268(15):11239-46. PubMed ID: 8496179
    [Abstract] [Full Text] [Related]

  • 5. Synthesis of (22R and 22S)-3 alpha, 7 alpha, 22-trihydroxy-5 beta-cholan-24-oic acids and structure of haemulcholic acid, a unique bile acid isolated from fish bile.
    Kihira K, Morioka Y, Hoshita T.
    J Lipid Res; 1981 Nov 25; 22(8):1181-7. PubMed ID: 7320628
    [Abstract] [Full Text] [Related]

  • 6. Chemical Synthesis of Rare Natural Bile Acids: 11α-Hydroxy Derivatives of Lithocholic and Chenodeoxycholic Acids.
    Namegawa K, Iida K, Omura K, Ogawa S, Hofmann AF, Iida T.
    Lipids; 2018 Apr 25; 53(4):403-411. PubMed ID: 29520792
    [Abstract] [Full Text] [Related]

  • 7. Synthesis and absolute configuration at C-23 of [23R and 23S]-3 alpha, 7 alpha, 23-trihydroxy-5 beta-cholan-24-oic and [23R and 23S]-3 alpha, 7 alpha, 12 alpha, 23-tetrahydroxy-5 beta-cholan-24-oic acids.
    Kutner A, Jaworska R.
    Steroids; 1982 Jul 25; 40(1):11-22. PubMed ID: 7157443
    [Abstract] [Full Text] [Related]

  • 8. 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 25; 75(7):506-12. PubMed ID: 20359489
    [Abstract] [Full Text] [Related]

  • 9. 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 25; 26(10):1205-11. PubMed ID: 4067415
    [Abstract] [Full Text] [Related]

  • 10. Epimerization versus dehydroxylation of the 7 alpha-hydroxyl- group of primary bile acids: competitive studies with Clostridium absonum and 7 alpha-dehydroxylating bacteria (Eubacterium sp.).
    Macdonald IA, Hutchison DM.
    J Steroid Biochem; 1982 Sep 25; 17(3):295-303. PubMed ID: 6957693
    [Abstract] [Full Text] [Related]

  • 11. Physicochemical and biological properties of natural and synthetic C-22 and C-23 hydroxylated bile acids.
    Roda A, Grigolo B, Minutello A, Pellicciari R, Natalini B.
    J Lipid Res; 1990 Feb 25; 31(2):289-98. PubMed ID: 2324648
    [Abstract] [Full Text] [Related]

  • 12. Identification of 3 beta, 7 beta-dihydroxy-5 beta-cholan-24-oic acid in serum from patients treated with ursodeoxycholic acid.
    Maeda M, Ohama H, Takeda H, Yabe M, Nambu M, Namihisa T.
    J Lipid Res; 1984 Jan 25; 25(1):14-26. PubMed ID: 6707518
    [Abstract] [Full Text] [Related]

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  • 14. 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 25; 57(3):107-11. PubMed ID: 1621264
    [Abstract] [Full Text] [Related]

  • 15. Bile acids with cyclopropane-containing side chain. 2. Synthesis and properties of 3 alpha,7 beta-dihydroxy-22,23-methylene-5 beta-cholan-24-oic acid (2-sulfoethyl)amide.
    Pellicciari R, Cecchetti S, Natalini B, Roda A, Grigolo B, Fini A.
    J Med Chem; 1985 Feb 25; 28(2):239-42. PubMed ID: 3968688
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  • 17. Synthesis of sulfonate analogs of bile acids.
    Kihira K, Mikami T, Ikawa S, Okamoto A, Yoshii M, Miki S, Mosbach EH, Hoshita T.
    Steroids; 1992 Apr 25; 57(4):193-8. PubMed ID: 1519263
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  • 19. Synthesis of the 1 beta-hydroxylated bile acids and identification of 1 beta,3 alpha,7 alpha-trihydroxy- and 1 beta,3 alpha,7 alpha,12 alpha-tetrahydroxy-5 beta-cholan-24-oic acids in human meconium.
    Tohma M, Mahara R, Takeshita H, Kurosawa T, Ikegawa S, Nittono H.
    Chem Pharm Bull (Tokyo); 1985 Jul 25; 33(7):3071-3. PubMed ID: 4085062
    [No Abstract] [Full Text] [Related]

  • 20. Synthesis of 19-hydroxylated bile acids and identification of 3 alpha,7 alpha,12 alpha,19-tetrahydroxy-5 beta-cholan-24-oic acid in human neonatal urine.
    Kurosawa T, Nomura Y, Mahara R, Yoshimura T, Kimura A, Ikegawa S, Tohma M.
    Chem Pharm Bull (Tokyo); 1995 Sep 25; 43(9):1551-7. PubMed ID: 7586081
    [Abstract] [Full Text] [Related]


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