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Volumn 61, Issue 11, 1996, Pages 639-641

Formation of varanic acid, 3α,7α,12α,24-tetrahydroxy-5β- cholestanoic acid from 3α,7α,12α-trihydroxy-5β-cholestanoic acid in Bombina orientalis

Author keywords

bile acid; Bombina orientalis; hydroxylation; varanic acid; oxidation

Indexed keywords

BILE ACID; UNCLASSIFIED DRUG; VARANIC ACID;

EID: 0030298373     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(96)00137-7     Document Type: Article
Times cited : (9)

References (11)
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  • 4
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    • Casteels, M.1    Schepers, L.2    Parmentier, G.3    Eyssen, H.J.4    Mannaert, G.P.5
  • 6
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    • Synthesis of four stereoisomers at carbons 24 and 25 of 3α, 7α, 12α,24-tetrahydroxy-5β-cholestan-26-oic acid, intermediates of bile acid biosynthesis
    • 6. Une M, Nagai F, Kihira K, Kuramoto T, Hoshita T (1983). Synthesis of four stereoisomers at carbons 24 and 25 of 3α, 7α, 12α,24-tetrahydroxy-5β-cholestan-26-oic acid, intermediates of bile acid biosynthesis. J Lipid Res 24:924-929.
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    • Synthesis and determination of stereochemistry of four diastereoisomers at the C-24 and C-25 position of 3α, 7α, 12α,24-tetrahydroxy-5β-cholestanoic acid
    • 8. Kinoshita T, Miyata M, Ismail SM, Fujimoto Y, Kakinuma K, Ikekawa N, Morisaki M (1988). Synthesis and determination of stereochemistry of four diastereoisomers at the C-24 and C-25 position of 3α, 7α, 12α,24-tetrahydroxy-5β-cholestanoic acid. Chem. Pharm. Bull (Tokyo) 36:134-141.
    • (1988) Chem. Pharm. Bull (Tokyo) , vol.36 , pp. 134-141
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  • 9
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    • Synthesis of diastereoisomers of 3α, 7α, 12α,24-tetrahydroxy- and 3α, 7α,24-trihydroxy-5β-cholestan-26-oic acids and their structure
    • 9. Kurosawa T, Sato M, Nakano H, Tohma M (1996). Synthesis of diastereoisomers of 3α, 7α, 12α,24-tetrahydroxy- and 3α, 7α,24-trihydroxy-5β-cholestan-26-oic acids and their structure. Steroids 61:421-428.
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  • 10
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    • Stereospecific formation of (24E)-3α, 7α, 12α-trihydroxy-5β-cholest-24-en-26-oic acid and (24R,25S)-3α, 7α, 12α-24-tetrahydroxy-5β-cholestan-26-oic acid from either (25R)- or (25S)-3α, 7α, 12α-trihydroxy-5β-cholestan-26-oic acid by rat liver homogenate
    • 10. Une M, Morigami I, Kihira K, Hoshita T (1984). Stereospecific formation of (24E)-3α, 7α, 12α-trihydroxy-5β-cholest-24-en-26-oic acid and (24R,25S)-3α, 7α, 12α-24-tetrahydroxy-5β-cholestan-26-oic acid from either (25R)- or (25S)-3α, 7α, 12α-trihydroxy-5β-cholestan-26-oic acid by rat liver homogenate. J Biochem 96:1103-1107.
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  • 11
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    • Identification of (24E)-3α, 7α-dihydroxy-5β-cholest-24-enoic acid and (24R,25S)-3α, 7α,24-trihydroxy-5β-cholestanoic acid as intermediates in the conversion of 3α, 7α-dihydroxy-5β-cholestanoic acid to chenodeoxycholic acid in rat liver homogenates
    • 11. Une M, Inoue A, Kurosawa T, Tohma M, Hoshita T (1994). Identification of (24E)-3α, 7α-dihydroxy-5β-cholest-24-enoic acid and (24R,25S)-3α, 7α,24-trihydroxy-5β-cholestanoic acid as intermediates in the conversion of 3α, 7α-dihydroxy-5β-cholestanoic acid to chenodeoxycholic acid in rat liver homogenates. J Lipid Res 35: 620-624.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.