[go: up one dir, main page]

TOHMA et al., 1981 - Google Patents

Quantitative determination of ursodeoxycholic acid and its deuterated derivative in human bile by gas chromatography-mass fragmentography

TOHMA et al., 1981

View PDF
Document ID
854954593360179171
Author
TOHMA M
NAKATA Y
YAMADA H
KUROSAWA T
MAKINO I
NAKAGAWA S
Publication year
Publication venue
Chemical and Pharmaceutical Bulletin

External Links

Snippet

抄録 Deuterium-labeled ursodeoxycholic acid (UDCA-d 2) was synthesized from cholic acid by heterogeneous catalytic reduction of the 11, 12-unsaturated bile acid with deuterium gas. A new method for the simultaneous determination of UDCA, UDCA-d 2, related bile acids …
Continue reading at www.jstage.jst.go.jp (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J7/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms
    • C07J7/0005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21
    • C07J7/001Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group
    • C07J7/0015Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group not substituted in position 17 alfa
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J9/00Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
    • C07J9/005Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J41/00Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
    • C07J41/0033Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J71/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton is condensed with a heterocyclic ring
    • C07J71/0036Nitrogen-containing hetero ring
    • C07J71/0042Nitrogen only
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J1/00Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J13/00Normal steroids containing carbon, hydrogen, halogen or oxygen having a carbon-to-carbon double bond from or to position 17
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J75/00Processes for the preparation of steroids in general
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J53/00Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by condensation with a carbocyclic rings or by formation of an additional ring by means of a direct link between two ring carbon atoms, including carboxyclic rings fused to the cyclopenta(a)hydrophenanthrene skeleton are included in this class
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J51/00Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07JSTEROIDS
    • C07J17/00Normal steroids containing carbon, hydrogen, halogen or oxygen, having an oxygen-containing hetero ring not condensed with the cyclopenta(a)hydrophenanthrene skeleton

Similar Documents

Publication Publication Date Title
Jolad et al. Constituents of Trichilia hispida (Meliaceae). 4. Hispidols A and B, two new tirucallane triterpenoids
TOHMA et al. Synthesis of the 1β-hydroxylated bile acids, unusual bile acids in human biological fluids
Cowen et al. Synthesis of 11, 12-2H2-and 11, 12-3H2-labeled chenodeoxycholic and lithocholic acids
Karim et al. Spironolactone metabolism in man studied by gas chromatography-mass spectrometry
TOHMA et al. Quantitative determination of ursodeoxycholic acid and its deuterated derivative in human bile by gas chromatography-mass fragmentography
Varma et al. Synthesis and C-25 chirality of 26-hydroxycholesterols
Biggerstaff et al. 3, 16β-Dihydroxy-Δ1, 3, 5-estratrien-17-one and Related Compounds1
Tal et al. Bile acids LXIX. Selective K-selectride reduction of 3, 7-diketo steroids
Bi et al. Studies on anabolic steroids—8. GC/MS characterization of unusual seco acidic metabolites of oxymetholone in human urine
Dayal et al. Preparation of 24 (R)-and 24 (S)-5β-cholestane-3α, 7α, 24-triols and 25 (R)-and 25 (S)-5β-cholestane-3α, 7α, 26-triols by a hydroboration procedure
Galli-Kienle et al. Reduction of. DELTA. 24 of lanosterol in the biosynthesis of cholesterol by rat liver enzymes. II. Stereochemistry of addition of the C-25 proton
Hanson et al. The isolation and identification of 3 alpha, 7 alpha-dihydroxy-5 beta-cholestan-26-oic acid from human bile
Kimura et al. Synthesis, intestinal absorption and metabolism of sarcosine conjugated ursodeoxycholic acid
SONODA et al. A simplified synthesis of 32-oxygenated lanosterol derivatives
Goto et al. Synthesis of conjugated cholesterol and cholestanols
Toshifumi et al. Synthesis of N-acetylglucosaminides of unconjugated and conjugated bile acids
NAMBARA et al. Studies on Metabolism of 3-Desoxyestrone. II. Isolation and Characterization of Urinary Metabolites of 3-Desoxyestrone in Rabbit
Tohma et al. Determination of 3β-hydroxy-5-cholen-24-OIC acid and its sulfate in human serum by gas chromatography-mass spectrometry
Fujimoto et al. A Preparation of β-Sitosterol1a
Kamat et al. Bile acids XXXVI. Synthesis of 5α-cholestan-26-oic acids
Kuramoto et al. Identification of short side chain bile acids in urine of patients with cerebrotendinous xanthomatosis
Arimoto et al. 7β, 12β-Dihydroxy-5β-cholan-24-oic acid as an internal standard for quantitative determination of bile acids by gas chromatography
NAKAGAWA et al. Synthesis of 2, 3, 17 β-Trihydroxyestra-1, 3, 5 (10)-trien-6-one and Its Related Compounds
OHMOTO et al. Constituents of Pollen. VIII. Constituents of Podocarpus macrophylla D. DON
NUMAZAWA et al. Synthesis of deuterium-labelled estriol, 16α-hydroxyestrone and estriol 16-glucuronide via 2, 4, 16α-tribromoestrone as internal standards for mass fragmentography