Drug metabolism (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Drug metabolism" in English language version.

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  • Jakoby WB, Ziegler DM (December 1990). "The enzymes of detoxication". J. Biol. Chem. 265 (34): 20715–8. doi:10.1016/S0021-9258(17)45272-0. PMID 2249981. Archived from the original on 2009-06-21. Retrieved 2012-12-29.
  • Omura T, Sato R (April 1962). "A new cytochrome in liver microsomes". J. Biol. Chem. 237 (4): 1375–6. doi:10.1016/S0021-9258(18)60338-2. PMID 14482007. Archived from the original on 2009-06-21. Retrieved 2012-12-29.

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  • Mizuno N, Niwa T, Yotsumoto Y, Sugiyama Y (September 2003). "Impact of drug transporter studies on drug discovery and development". Pharmacol. Rev. 55 (3): 425–61. doi:10.1124/pr.55.3.1. PMID 12869659. S2CID 724685.
  • Liston HL, Markowitz JS, DeVane CL (October 2001). "Drug glucuronidation in clinical psychopharmacology". J Clin Psychopharmacol. 21 (5): 500–15. doi:10.1097/00004714-200110000-00008. PMID 11593076. S2CID 6068811.
  • Badenhorst CP, van der Sluis R, Erasmus E, van Dijk AA (September 2013). "Glycine conjugation: importance in metabolism, the role of glycine N-acyltransferase, and factors that influence interindividual variation". Expert Opinion on Drug Metabolism & Toxicology. 9 (9): 1139–1153. doi:10.1517/17425255.2013.796929. PMID 23650932. S2CID 23738007. Glycine conjugation of mitochondrial acyl-CoAs, catalyzed by glycine N-acyltransferase (GLYAT, E.C. 2.3.1.13), is an important metabolic pathway responsible for maintaining adequate levels of free coenzyme A (CoASH). However, because of the small number of pharmaceutical drugs that are conjugated to glycine, the pathway has not yet been characterized in detail. Here, we review the causes and possible consequences of interindividual variation in the glycine conjugation pathway. ...
    Figure 1. Glycine conjugation of benzoic acid. The glycine conjugation pathway consists of two steps. First benzoate is ligated to CoASH to form the high-energy benzoyl-CoA thioester. This reaction is catalyzed by the HXM-A and HXM-B medium-chain acid:CoA ligases and requires energy in the form of ATP. ... The benzoyl-CoA is then conjugated to glycine by GLYAT to form hippuric acid, releasing CoASH. In addition to the factors listed in the boxes, the levels of ATP, CoASH, and glycine may influence the overall rate of the glycine conjugation pathway.
  • Homolya L, Váradi A, Sarkadi B (2003). "Multidrug resistance-associated proteins: Export pumps for conjugates with glutathione, glucuronate or sulfate". BioFactors. 17 (1–4): 103–14. doi:10.1002/biof.5520170111. PMID 12897433. S2CID 7744924.
  • Rostami-Hodjegan A, Tucker GT (February 2007). "Simulation and prediction of in vivo drug metabolism in human populations from in vitro data". Nat Rev Drug Discov. 6 (2): 140–8. doi:10.1038/nrd2173. PMID 17268485. S2CID 205476485.

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  • Jakoby WB, Ziegler DM (December 1990). "The enzymes of detoxication". J. Biol. Chem. 265 (34): 20715–8. doi:10.1016/S0021-9258(17)45272-0. PMID 2249981. Archived from the original on 2009-06-21. Retrieved 2012-12-29.
  • "Acetonitrile (EHC 154, 1993)". www.inchem.org. Archived from the original on 2017-05-22. Retrieved 2017-05-03.
  • Murphy PJ (June 2001). "Xenobiotic metabolism: a look from the past to the future". Drug Metab. Dispos. 29 (6): 779–80. PMID 11353742. Archived from the original on 2009-06-21. Retrieved 2012-12-29.
  • Omura T, Sato R (April 1962). "A new cytochrome in liver microsomes". J. Biol. Chem. 237 (4): 1375–6. doi:10.1016/S0021-9258(18)60338-2. PMID 14482007. Archived from the original on 2009-06-21. Retrieved 2012-12-29.

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