Kong TY - Search Results

1

Evaluation of DA-9801, a new herbal drug for diabetic neuropathy, on metabolism-mediated interaction.

Ji HY, Liu KH, Kong TY, Jeong HU, Choi SZ, Son M, Cho YY, Lee HS. Ji HY, et al. Among authors: kong ty. Arch Pharm Res. 2013 Jan;36(1):1-5. doi: 10.1007/s12272-013-0014-9. Arch Pharm Res. 2013. PMID: 23371804

2

Effect of honokiol on cytochrome P450 and UDP-glucuronosyltransferase enzyme activities in human liver microsomes.

Jeong HU, Kong TY, Kwon SS, Hong SW, Yeon SH, Choi JH, Lee JY, Cho YY, Lee HS. Jeong HU, et al. Among authors: kong ty. Molecules. 2013 Sep 3;18(9):10681-93. doi: 10.3390/molecules180910681. Molecules. 2013. PMID: 24005963 Free PMC article.

3

Evaluation of the transporter-mediated herb-drug interaction potential of DA-9801, a standardized dioscorea extract for diabetic neuropathy, in human in vitro and rat in vivo.

Song IS, Kong TY, Jeong HU, Kim EN, Kwon SS, Kang HE, Choi SZ, Son M, Lee HS. Song IS, et al. Among authors: kong ty. BMC Complement Altern Med. 2014 Jul 17;14:251. doi: 10.1186/1472-6882-14-251. BMC Complement Altern Med. 2014. PMID: 25034211 Free PMC article.

4

Inhibitory effects of cedrol, β-cedrene, and thujopsene on cytochrome P450 enzyme activities in human liver microsomes.

Jeong HU, Kwon SS, Kong TY, Kim JH, Lee HS. Jeong HU, et al. Among authors: kong ty. J Toxicol Environ Health A. 2014;77(22-24):1522-32. doi: 10.1080/15287394.2014.955906. J Toxicol Environ Health A. 2014. PMID: 25343299

5

Comparative metabolism of honokiol in mouse, rat, dog, monkey, and human hepatocytes.

Jeong HU, Kim JH, Kong TY, Choi WG, Lee HS. Jeong HU, et al. Among authors: kong ty. Arch Pharm Res. 2016 Apr;39(4):516-530. doi: 10.1007/s12272-016-0731-y. Epub 2016 Mar 16. Arch Pharm Res. 2016. PMID: 26983827

6

Inhibition of cytochrome P450 and uridine 5'-diphospho-glucuronosyltransferases by MAM-2201 in human liver microsomes.

Kong TY, Kim JH, Kwon SS, Cheong JC, Kim HS, In MK, Lee HS. Kong TY, et al. Arch Pharm Res. 2017 Jun;40(6):727-735. doi: 10.1007/s12272-017-0917-y. Epub 2017 May 8. Arch Pharm Res. 2017. PMID: 28484907

7

Synthetic cannabinoids are substrates and inhibitors of multiple drug-metabolizing enzymes.

Kong TY, Kim JH, Kim DK, Lee HS. Kong TY, et al. Arch Pharm Res. 2018 Jul;41(7):691-710. doi: 10.1007/s12272-018-1055-x. Epub 2018 Jul 23. Arch Pharm Res. 2018. PMID: 30039377 Review.

8

In vitro metabolism of a novel synthetic cannabinoid, EAM-2201, in human liver microsomes and human recombinant cytochrome P450s.

Kim JH, Kim HS, Kong TY, Lee JY, Kim JY, In MK, Lee HS. Kim JH, et al. Among authors: kong ty. J Pharm Biomed Anal. 2016 Feb 5;119:50-8. doi: 10.1016/j.jpba.2015.11.023. Epub 2015 Nov 22. J Pharm Biomed Anal. 2016. PMID: 26641707

9

Rapid analysis of drugs of abuse and their metabolites in human urine using dilute and shoot liquid chromatography-tandem mass spectrometry.

Kong TY, Kim JH, Kim JY, In MK, Choi KH, Kim HS, Lee HS. Kong TY, et al. Arch Pharm Res. 2017 Feb;40(2):180-196. doi: 10.1007/s12272-016-0862-1. Epub 2016 Dec 17. Arch Pharm Res. 2017. PMID: 27988881

10

AM-2201 Inhibits Multiple Cytochrome P450 and Uridine 5'-Diphospho-Glucuronosyltransferase Enzyme Activities in Human Liver Microsomes.

Kim JH, Kwon SS, Kong TY, Cheong JC, Kim HS, In MK, Lee HS. Kim JH, et al. Among authors: kong ty. Molecules. 2017 Mar 10;22(3):443. doi: 10.3390/molecules22030443. Molecules. 2017. PMID: 28287454 Free PMC article.

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