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86 related items for PubMed ID: 10368924
1. Sex differences in stereospecificity of oracin reductases in rat in vitro and in vivo. Wsól V, Skálová L, Szotáková B, Trejtnar F, Kvasnicková E. Chirality; 1999; 11(5-6):505-9. PubMed ID: 10368924 [Abstract] [Full Text] [Related]
2. A comparison between stereospecificity of oracin reduction and stereoselectivity of oxidation of 11-dihydrooracin enantiomers in vitro in rat and guinea pig. Skálová L, Wsól V, Szotáková B, Kvasnicková E. Chirality; 1999; 11(5-6):510-5. PubMed ID: 10368925 [Abstract] [Full Text] [Related]
3. Stereospecific reduction of the original anticancer drug oracin in rat extrahepatic tissues. Szotáková B, Skálová L, Jílek P, Buchta V, Wsól V. J Pharm Pharmacol; 2003 Jul; 55(7):1003-11. PubMed ID: 12906758 [Abstract] [Full Text] [Related]
4. The main metabolic pathway of oracin, a new potential cytostatic drug, in human liver microsomes and cytosol: stereoselectivity of reoxidation of the principal metabolite 11-dihydrooracin to oracin. Wsól V, Szotáková B, Skálová L, Cepková H, Kvasnicková E. Enantiomer; 2000 Jul; 5(3-4):263-70. PubMed ID: 11126866 [Abstract] [Full Text] [Related]
5. Partial purification and characterization of a new human membrane-bound carbonyl reductase playing a role in the deactivation of the anticancer drug oracin. Skarydová L, Skarka A, Novotná R, Zivná L, Martin HJ, Wsól V, Maser E. Toxicology; 2009 Oct 01; 264(1-2):52-60. PubMed ID: 19635524 [Abstract] [Full Text] [Related]
6. Aldo-keto reductases (AKR) from the AKR1C subfamily catalyze the carbonyl reduction of the novel anticancer drug oracin in man. Wsol V, Szotakova B, Martin HJ, Maser E. Toxicology; 2007 Sep 05; 238(2-3):111-8. PubMed ID: 17618725 [Abstract] [Full Text] [Related]
7. High-performance liquid chromatography study of stereospecific microsomal enzymes catalysing the reduction of a potential cytostatic drug, oracin. Interspecies comparison. Wsól V, Szotáková B, Kvasnicková E, Fell AF. J Chromatogr A; 1998 Feb 27; 797(1-2):197-201. PubMed ID: 9542111 [Abstract] [Full Text] [Related]
8. The novel anticancer drug oracin: different stereospecificity and cooperativity for carbonyl reduction by purified human liver 11beta-hydroxysteroid dehydrogenase type 1. Wsól V, Szotáková B, Skálová L, Maser E. Toxicology; 2004 May 03; 197(3):253-61. PubMed ID: 15033547 [Abstract] [Full Text] [Related]
9. Reduction of the potential anticancer drug oracin in the rat liver in-vitro. Szotáková B, Skálová L, Wsól V, Kvasniècková E. J Pharm Pharmacol; 2000 May 03; 52(5):495-500. PubMed ID: 10864136 [Abstract] [Full Text] [Related]
10. Stereochemical aspects of carbonyl reduction of the original anticancer drug oracin by mouse liver microsomes and purified 11beta-hydroxysteroid dehydrogenase type 1. Wsól V, Szotáková B, Skálová L, Maser E. Chem Biol Interact; 2003 Feb 01; 143-144():459-68. PubMed ID: 12604232 [Abstract] [Full Text] [Related]
11. Activity, stereospecificity, and stereoselectivity of microsomal enzymes in dependence on storage and freezing of rat liver samples. Skálová L, Szotáková B, Wsól V, Král R, Baliharová V, Lamka J. Chirality; 2000 Oct 01; 12(9):649-53. PubMed ID: 10984737 [Abstract] [Full Text] [Related]
12. Stereospecificity and stereoselectivity of flobufen metabolic profile in male rats in vitro and in vivo: phase I of biotransformation. Wsól V, Král R, Skálová L, Szotáková B, Trejtnar F, Flieger M. Chirality; 2001 Oct 01; 13(10):754-9. PubMed ID: 11746815 [Abstract] [Full Text] [Related]
13. Stereospecificity of flobufen metabolism in guinea pigs in vitro and in vivo: phase I of biotransformation. Kral R, Skalova L, Szotakova B, Babu YN, Wsol V. Chirality; 2004 Jan 01; 16(1):1-9. PubMed ID: 14628293 [Abstract] [Full Text] [Related]
14. Central composite design as a powerful optimisation technique for enantioresolution of the rac-11-dihydrooracin--the principal metabolite of the potential cytostatic drug oracin. Wsól V, Fell AF. J Biochem Biophys Methods; 2002 Dec 31; 54(1-3):377-90. PubMed ID: 12543513 [Abstract] [Full Text] [Related]
15. Reduction of doxorubicin and oracin and induction of carbonyl reductase in human breast carcinoma MCF-7 cells. Gavelová M, Hladíková J, Vildová L, Novotná R, Vondrácek J, Krcmár P, Machala M, Skálová L. Chem Biol Interact; 2008 Oct 22; 176(1):9-18. PubMed ID: 18755171 [Abstract] [Full Text] [Related]
16. Warfarin: stereochemical aspects of its metabolism in vivo in the rat. Pohl LR, Bales R, Trager WF. Res Commun Chem Pathol Pharmacol; 1976 Oct 22; 15(2):233-56. PubMed ID: 981784 [Abstract] [Full Text] [Related]
17. Biotransformation of flobufen enantiomers in ruminant hepatocytes and subcellular fractions. Skálová L, Szotáková B, Lamka J, Král R, Vanková I, Baliharová V, Wsól V. Chirality; 2001 Oct 22; 13(10):760-4. PubMed ID: 11746816 [Abstract] [Full Text] [Related]
18. Use of chiral liquid chromatography for the evaluation of stereospecificity in the carbonyl reduction of potential benzo[c]fluorene antineoplastics benfluron and dimefluron in various species. Kucera R, Nobilis M, Skálová L, Szotáková B, Císar P, Jira T, Klimes J, Wsól V. J Pharm Biomed Anal; 2005 Apr 29; 37(5):1049-57. PubMed ID: 15862685 [Abstract] [Full Text] [Related]
19. High-performance liquid chromatographic assay for the separation and characterization of metabolites of the potential cytostatic drug oracine. Wsól V, Kvasnicková E, Szotáková B, Hais IM. J Chromatogr B Biomed Appl; 1996 May 31; 681(1):169-75. PubMed ID: 8798926 [Abstract] [Full Text] [Related]
20. Pharmacokinetics and metabolism of a cysteinyl leukotriene-1 receptor antagonist from the heterocyclic chromanol series in rats: in vitro-in vivo correlation, gender-related differences, isoform identification, and comparison with metabolism in human hepatic tissue. Kuperman AV, Kalgutkar AS, Marfat A, Chambers RJ, Liston TE. Drug Metab Dispos; 2001 Nov 31; 29(11):1403-9. PubMed ID: 11602515 [Abstract] [Full Text] [Related] Page: [Next] [New Search]