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Journal Abstract Search

242 related items for PubMed ID: 28031430

  • 1. Metabolic Disposition of Luteolin Is Mediated by the Interplay of UDP-Glucuronosyltransferases and Catechol-O-Methyltransferases in Rats.
    Wang L, Chen Q, Zhu L, Li Q, Zeng X, Lu L, Hu M, Wang X, Liu Z.
    Drug Metab Dispos; 2017 Mar; 45(3):306-315. PubMed ID: 28031430
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  • 3. Role of catechol-O-methyltransferase in the disposition of luteolin in rats.
    Chen Z, Chen M, Pan H, Sun S, Li L, Zeng S, Jiang H.
    Drug Metab Dispos; 2011 Apr; 39(4):667-74. PubMed ID: 21209248
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  • 4. A combined strategy of mass fragmentation, post-column cobalt complexation and shift in ultraviolet absorption spectra to determine the uridine 5'-diphospho-glucuronosyltransferase metabolism profiling of flavones after oral administration of a flavone mixture in rats.
    Li Q, Wang L, Dai P, Zeng X, Qi X, Zhu L, Yan T, Wang Y, Lu L, Hu M, Wang X, Liu Z.
    J Chromatogr A; 2015 May 22; 1395():116-28. PubMed ID: 25892633
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  • 5. UGT-mediated metabolism plays a dominant role in the pharmacokinetic behavior and the disposition of morusin in vivo and in vitro.
    Hou C, Liu W, Liang Z, Han W, Li J, Ye L, Liu M, Cai Z, Zhao J, Chen Y, Liu S, Tang L.
    J Pharm Biomed Anal; 2018 May 30; 154():339-353. PubMed ID: 29571132
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  • 7. Wedelolactone metabolism in rats through regioselective glucuronidation catalyzed by uridine diphosphate-glucuronosyltransferases 1As (UGT1As).
    Li L, Huang XJ, Peng JL, Zheng MY, Zhong DF, Zhang CF, Chen XY.
    Phytomedicine; 2016 Apr 15; 23(4):340-9. PubMed ID: 27002404
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  • 8. The human UDP-glucuronosyltransferase UGT1A3 is highly selective towards N2 in the tetrazole ring of losartan, candesartan, and zolarsartan.
    Alonen A, Finel M, Kostiainen R.
    Biochem Pharmacol; 2008 Sep 15; 76(6):763-72. PubMed ID: 18674515
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  • 9. Application of ultra high-performance liquid chromatography tandem mass spectrometry to investigate the regioselective glucuronidation of icaritin in vitro.
    Rong Y, Meng Z, Li J, Zhu X, Gan H, Gu R, Wu Z, Sun W, Liu T, Zheng Y, Jin M, Peng J, Wang X, Dou G.
    J Pharm Biomed Anal; 2018 May 30; 154():444-453. PubMed ID: 29587224
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  • 12. In vitro glucuronidation of thyroxine and triiodothyronine by liver microsomes and recombinant human UDP-glucuronosyltransferases.
    Tong Z, Li H, Goljer I, McConnell O, Chandrasekaran A.
    Drug Metab Dispos; 2007 Dec 30; 35(12):2203-10. PubMed ID: 17875670
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  • 13. Time-Dependent Metabolism of Luteolin by Human UDP-Glucuronosyltransferases and Its Intestinal First-Pass Glucuronidation in Mice.
    Wu L, Liu J, Han W, Zhou X, Yu X, Wei Q, Liu S, Tang L.
    J Agric Food Chem; 2015 Oct 07; 63(39):8722-33. PubMed ID: 26377048
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  • 14. The configuration of the 17-hydroxy group variably influences the glucuronidation of beta-estradiol and epiestradiol by human UDP-glucuronosyltransferases.
    Itäaho K, Mackenzie PI, Ikushiro S, Miners JO, Finel M.
    Drug Metab Dispos; 2008 Nov 07; 36(11):2307-15. PubMed ID: 18719240
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  • 16. Glucuronidation of anabolic androgenic steroids by recombinant human UDP-glucuronosyltransferases.
    Kuuranne T, Kurkela M, Thevis M, Schänzer W, Finel M, Kostiainen R.
    Drug Metab Dispos; 2003 Sep 07; 31(9):1117-24. PubMed ID: 12920167
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  • 19. Glucuronidation of edaravone by human liver and kidney microsomes: biphasic kinetics and identification of UGT1A9 as the major UDP-glucuronosyltransferase isoform.
    Ma L, Sun J, Peng Y, Zhang R, Shao F, Hu X, Zhu J, Wang X, Cheng X, Zhu Y, Wan P, Feng D, Wu H, Wang G.
    Drug Metab Dispos; 2012 Apr 07; 40(4):734-41. PubMed ID: 22238289
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