Page last updated: 2024-08-16

propofol and hymecromone

propofol has been researched along with hymecromone in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (57.14)29.6817
2010's3 (42.86)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Strassburg, CP; Tukey, RH1
Kamimura, H; Mano, Y; Usui, T2
Knights, KM; Mackenzie, PI; Miners, JO; Rowland, A1
Fang, ZZ; Ge, GB; Liang, SC; Liu, HX; Mao, YX; Shang, HT; Wei, H; Yang, L; Zhu, LL1
Bai, MC; Guo, YL; Wang, CM; Yang, Y; Yu, ML; Zhang, MM1
Ge, GB; Hao, DC; Hou, J; Hu, WZ; Liu, SW; Lv, X; Shi, YS; Wang, XX; Yang, L; Zhang, JB; Zhang, WD1

Reviews

1 review(s) available for propofol and hymecromone

ArticleYear
Human UDP-glucuronosyltransferases: metabolism, expression, and disease.
    Annual review of pharmacology and toxicology, 2000, Volume: 40

    Topics: Autoimmunity; Chromosome Mapping; Glucuronides; Glucuronosyltransferase; Humans; Hyperbilirubinemia; Neoplasms; Steroids; Terminology as Topic

2000

Other Studies

6 other study(ies) available for propofol and hymecromone

ArticleYear
Effects of beta-estradiol and propofol on the 4-methylumbelliferone glucuronidation in recombinant human UGT isozymes 1A1, 1A8 and 1A9.
    Biopharmaceutics & drug disposition, 2004, Volume: 25, Issue:8

    Topics: Cells, Cultured; Estradiol; Glucuronosyltransferase; Humans; Hymecromone; Hypnotics and Sedatives; Isoenzymes; Propofol

2004
Substrate-dependent modulation of UDP-glucuronosyltransferase 1A1 (UGT1A1) by propofol in recombinant human UGT1A1 and human liver microsomes.
    Basic & clinical pharmacology & toxicology, 2007, Volume: 101, Issue:3

    Topics: Estradiol; Ethinyl Estradiol; Glucuronides; Glucuronosyltransferase; Humans; Hymecromone; Microsomes, Liver; Propofol; Recombinant Proteins

2007
The "albumin effect" and drug glucuronidation: bovine serum albumin and fatty acid-free human serum albumin enhance the glucuronidation of UDP-glucuronosyltransferase (UGT) 1A9 substrates but not UGT1A1 and UGT1A6 activities.
    Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:6

    Topics: Adult; Aged; Animals; Cattle; Cell Line; Female; Glucuronides; Glucuronosyltransferase; Humans; Hymecromone; Male; Microsomes, Liver; Middle Aged; Propofol; Recombinant Proteins; Serum Albumin; Serum Albumin, Bovine; UDP-Glucuronosyltransferase 1A9

2008
Determination of propofol UDP-glucuronosyltransferase (UGT) activities in hepatic microsomes from different species by UFLC-ESI-MS.
    Journal of pharmaceutical and biomedical analysis, 2011, Jan-05, Volume: 54, Issue:1

    Topics: Acetic Acid; Animals; Calibration; Dogs; Glucuronosyltransferase; Haplorhini; Humans; Hymecromone; Kinetics; Mass Spectrometry; Mice; Microsomes, Liver; Models, Chemical; Propofol; Rats; Reproducibility of Results; Spectrometry, Mass, Electrospray Ionization

2011
Acitretin exhibits inhibitory effects towards UDP-glucuronosyltransferase (UGT)1A9-mediated 4-methylumbelliferone (4-MU) and propofol glucuronidation reaction.
    Die Pharmazie, 2013, Volume: 68, Issue:6

    Topics: Acitretin; Chromatography, High Pressure Liquid; Dose-Response Relationship, Drug; Glucuronides; Glucuronosyltransferase; Humans; Hymecromone; In Vitro Techniques; Isoenzymes; Keratolytic Agents; Kinetics; Liver; Microsomes, Liver; Propofol; UDP-Glucuronosyltransferase 1A9

2013
Amentoflavone is a potent broad-spectrum inhibitor of human UDP-glucuronosyltransferases.
    Chemico-biological interactions, 2018, Mar-25, Volume: 284

    Topics: Biflavonoids; Chromatography, High Pressure Liquid; Glucuronosyltransferase; Humans; Hymecromone; Inhibitory Concentration 50; Kinetics; Microsomes, Liver; Propofol; Recombinant Proteins

2018
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