Page last updated: 2024-09-04

s 8921 and uridine diphosphate glucuronic acid

s 8921 has been researched along with uridine diphosphate glucuronic acid in 1 studies

Compound Research Comparison

Studies
(s 8921)
Trials
(s 8921)
Recent Studies (post-2010)
(s 8921)
Studies
(uridine diphosphate glucuronic acid)
Trials
(uridine diphosphate glucuronic acid)
Recent Studies (post-2010) (uridine diphosphate glucuronic acid)
1100502271

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baba, T; Hara, S; Horie, K; Kanazu, T; Kusuhara, H; Matsuo, Y; Miyata, K; Nomura, K; Okamura, N; Sakamoto, S; Shimaoka, H; Sugiyama, Y1

Other Studies

1 other study(ies) available for s 8921 and uridine diphosphate glucuronic acid

ArticleYear
Glucuronidation converting methyl 1-(3,4-dimethoxyphenyl)-3-(3-ethylvaleryl)-4-hydroxy-6,7,8-trimethoxy-2-naphthoate (S-8921) to a potent apical sodium-dependent bile acid transporter inhibitor, resulting in a hypocholesterolemic action.
    The Journal of pharmacology and experimental therapeutics, 2007, Volume: 322, Issue:2

    Topics: Animals; Anticholesteremic Agents; Cell Line; Cells, Cultured; Cholesterol; Cholesterol, HDL; Glucuronosyltransferase; Hepatocytes; Humans; Hypercholesterolemia; Intestinal Absorption; Kinetics; Male; Molecular Structure; Naphthols; Organic Anion Transporters, Sodium-Dependent; Portal Vein; Rats; Rats, Gunn; Rats, Wistar; Symporters; Taurocholic Acid; Transfection; Uridine Diphosphate Glucuronic Acid

2007