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Volumn 68, Issue 9, 2003, Pages 733-738

Synthesis of deuterated isotopomers of 7α- and (25R,S)-26- hydroxycholesterol, internal standards for in vivo determination of the two biosynthetic pathways of bile acids

Author keywords

(25R) 26 hydroxycholesterol; 7 hydroxycholesterol; Bile acids; Cholesterol metabolism; Deuterated isotopomers

Indexed keywords

26 HYDROXYCHOLESTEROL; 7ALPHA HYDROXYCHOLESTEROL; BILE ACID; CHOLESTEROL DERIVATIVE; DEUTERIUM; PREGNANE DERIVATIVE; STEROL;

EID: 0242624541     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(03)00116-8     Document Type: Article
Times cited : (11)

References (15)
  • 1
    • 0026551710 scopus 로고
    • Mechanism of degradation of the steroid side chain in the formation of bile acids
    • Bjoerkhem I. Mechanism of degradation of the steroid side chain in the formation of bile acids. J. Lipid Res. 33:1992;455-471.
    • (1992) J. Lipid Res. , vol.33 , pp. 455-471
    • Bjoerkhem, I.1
  • 2
    • 0032769064 scopus 로고    scopus 로고
    • 27-Hydroxycholesterol: Production rates in normal human subjects
    • Duane W.C., Javitt N.B. 27-Hydroxycholesterol: production rates in normal human subjects. J. Lipid Res. 40:1999;1194-1199.
    • (1999) J. Lipid Res. , vol.40 , pp. 1194-1199
    • Duane, W.C.1    Javitt, N.B.2
  • 3
    • 0035063560 scopus 로고    scopus 로고
    • Cholesterol metabolism in primary biliary cirrhosis during simvastatin and UDCA administration
    • Del Puppo M., Galli Kienle M., Crosignani A., Petroni M.L., Amati B., Zuin M.et al. Cholesterol metabolism in primary biliary cirrhosis during simvastatin and UDCA administration. J. Lipid Res. 42:2001;437-441.
    • (2001) J. Lipid Res. , vol.42 , pp. 437-441
    • Del Puppo, M.1    Galli Kienle, M.2    Crosignani, A.3    Petroni, M.L.4    Amati, B.5    Zuin, M.6
  • 4
    • 0020051430 scopus 로고
    • Cholest-5-ene-3β,26-diol: Synthesis and biomedical use of a deuterated compound
    • Javitt N.B., Kok E., Lloyd J., Benscath A., Field F.H. Cholest-5-ene-3β,26-diol: synthesis and biomedical use of a deuterated compound. Biom. Mass. Spectrom. 9:1982;61-63.
    • (1982) Biom. Mass. Spectrom. , vol.9 , pp. 61-63
    • Javitt, N.B.1    Kok, E.2    Lloyd, J.3    Benscath, A.4    Field, F.H.5
  • 6
    • 0027212186 scopus 로고
    • A revisitation of the Clemmensen reduction of diosgenin. Characterization of byproducts and their use in the preparation of (25R)-26-hydroxysterols
    • Ni Y., Kim H.-S., Wilson W.K., Kisic A., Schroepfer G.J. Jr. A revisitation of the Clemmensen reduction of diosgenin. Characterization of byproducts and their use in the preparation of (25R)-26-hydroxysterols. Tetrahedron Lett. 34:1993;3687-3690.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 3687-3690
    • Ni, Y.1    Kim, H.-S.2    Wilson, W.K.3    Kisic, A.4    Schroepfer Jr., G.J.5
  • 7
    • 0037330693 scopus 로고    scopus 로고
    • 4 ]-3β-(tert-butyldimethylsilanyloxy)-20-methyl-pregn-5-en-21-ol, an useful intermediate for the preparation of deuterated isotopomers of sterols
    • 4 ]-3β-(tert- butyldimethylsilanyloxy)-20-methyl-pregn-5-en-21-ol, an useful intermediate for the preparation of deuterated isotopomers of sterols Steroids. 68:2003;193-198.
    • (2003) Steroids , vol.68 , pp. 193-198
    • Ciuffreda, P.1    Casati, S.2    Bollini, D.3    Santaniello, E.4
  • 8
    • 0002714675 scopus 로고
    • Rapid chromatographic technique for preparative separations with moderate resolution
    • Still W.C., Kahn M., Mitra A. Rapid chromatographic technique for preparative separations with moderate resolution. J. Org. Chem. 43:1978;2923-2925.
    • (1978) J. Org. Chem. , vol.43 , pp. 2923-2925
    • Still, W.C.1    Kahn, M.2    Mitra, A.3
  • 9
    • 0242539100 scopus 로고
    • Toad poisons. XXXI. Sterins and bufadienolides of the skin of Bufo formosus
    • Iseli E., Kotake M., Weiss E.K., Reichstein T. Toad poisons. XXXI. Sterins and bufadienolides of the skin of Bufo formosus. Helv. Chim. Acta. 48:1965;1093-1112.
    • (1965) Helv. Chim. Acta , vol.48 , pp. 1093-1112
    • Iseli, E.1    Kotake, M.2    Weiss, E.K.3    Reichstein, T.4
  • 10
    • 84959971999 scopus 로고
    • Stereospecific syntheses of 7β- and 7α-hydroxycholesterols
    • Kumar V., Amann A., Ourisson G., Luu B. Stereospecific syntheses of 7β- and 7α-hydroxycholesterols. Synth. Commun. 17:1987;1279-1286.
    • (1987) Synth. Commun. , vol.17 , pp. 1279-1286
    • Kumar, V.1    Amann, A.2    Ourisson, G.3    Luu, B.4
  • 11
    • 0018421101 scopus 로고
    • Steroidal ethers. Analogues of 7-ketocholesterol
    • Dygos J.H., Desai B.N. Steroidal ethers. Analogues of 7-ketocholesterol. J. Org. Chem. 44:1979;1590-1594.
    • (1979) J. Org. Chem. , vol.44 , pp. 1590-1594
    • Dygos, J.H.1    Desai, B.N.2
  • 12
    • 0242455445 scopus 로고
    • Synthèse d'aldéhydes ou de cétones par alkylation de carbanions β-carbonylés saturés ou éthylé niques masqués
    • Julia M., Badet B. Synthèse d'aldéhydes ou de cétones par alkylation de carbanions β-carbonylés saturés ou éthyléniques masqués. Bulletin de la Société Chimique de France. 5/6:1975;1363-1366.
    • (1975) Bulletin de la Société Chimique de France , vol.5-6 , pp. 1363-1366
    • Julia, M.1    Badet, B.2
  • 13
    • 0011163864 scopus 로고
    • New chemoenzymatic synthesis of (R)- and (S)-4-(phenylsulfonyl)-2-methyl- 1-butanol: A chiral C5 isoprenoid synthon
    • Ferraboschi P., Grisenti P., Manzocchi A., Santaniello E. New chemoenzymatic synthesis of (R)- and (S)-4-(phenylsulfonyl)-2-methyl-1-butanol: a chiral C5 isoprenoid synthon. J. Org. Chem. 55:1990;6214-6216.
    • (1990) J. Org. Chem. , vol.55 , pp. 6214-6216
    • Ferraboschi, P.1    Grisenti, P.2    Manzocchi, A.3    Santaniello, E.4
  • 14
    • 0030979913 scopus 로고    scopus 로고
    • Synthesis of two marine natural products: The aglycones of pavoninin-1 and 2
    • Kim H.-S., Kim I.-C., Lee S.-O. Synthesis of two marine natural products: the aglycones of pavoninin-1 and 2. Tetrahedron. 53:1997;8129-8136.
    • (1997) Tetrahedron , vol.53 , pp. 8129-8136
    • Kim, H.-S.1    Kim, I.-C.2    Lee, S.-O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.