General Information of DME (ID: DEB3CV1)

DME Name UDP-glucuronosyltransferase 2B7 (UGT2B7) DME Info
Gene Name UGT2B7

Molecule-Related Drug & Molecule List

Molecule-Related Drug List
Molecule Type:
DTT
DTP
DME
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Investigative Drug(s)
46 Approved Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Abacavir DMMN36E Human immunodeficiency virus infection 1C62 Approved [1]
Aldosterone DM9S2JW Hypertension BA00-BA04 Approved [2]
Ambrisentan DMD1QXW Pulmonary arterial hypertension BB01.0 Approved [3]
Anastrozole DMNP60F Breast cancer 2C60-2C65 Approved [4]
Bromfenac DMKB79O Pain MG30-MG3Z Approved [5]
Carbamazepine DMZOLBI Epilepsy 8A60-8A68 Approved [6]
Carprofen DMHMP05 Pain MG30-MG3Z Approved [7]
Carvedilol DMHTEAO Chronic heart failure BD1Z Approved [8]
Cenobamate DM8KLU9 Complex partial seizure 8A68.0 Approved [9]
Codeine DMJX6ZG Allergic rhinitis CA08.0 Approved [10]
Dapagliflozin DM28UJG Non-insulin dependent diabetes 5A11 Approved [11]
Dexibuprofen DMFYBD0 Ankylosing spondylitis FA92.0 Approved [12]
Diclofenac DMPIHLS Chronic renal failure GB61.Z Approved [12]
Dihydroartemisinin DMBXVMZ Malaria 1F40-1F45 Approved [13]
Empagliflozin DMRF9YK Type-1 diabetes 5A10 Approved [14]
Epirubicin DMPDW6T Solid tumour/cancer 2A00-2F9Z Approved [15]
Etodolac DM6WJO9 Osteoarthritis FA00-FA05 Approved [12]
Ezetimibe DM7A8TW Atherosclerosis BD40 Approved [16]
Flurbiprofen DMGN4BY Osteoarthritis FA00-FA05 Approved [12]
Gemfibrozil DMD8Q3J Hyperlipidaemia 5C80 Approved [17]
Hydromorphone DMHP21E Back pain ME84.Z Approved [18]
Ibuprofen DM8VCBE Dysmenorrhea GA34.3 Approved [12]
Indomethacin DMSC4A7 Bursitis Approved [19]
Ketorolac DMI4EL5 Postoperative inflammation 1A00-CA43.1 Approved [20]
Labetalol DMK8U72 Hypertension BA00-BA04 Approved [21]
Lorazepam DM84ZXF Absence epilepsy Approved [22]
Losartan DM72JXH Diabetic kidney disease GB61.Z Approved [12]
Lovastatin DM9OZWQ Arteriosclerosis BD40 Approved [23]
Morphine DMRMS0L Advanced cancer 2A00-2F9Z Approved [24]
Mycophenolate mofetil DMPQAGE Hepatosplenic T-cell lymphoma Approved [25]
Mycophenolic acid DMRBMAU Crohn disease DD70 Approved [26]
Naproxen DMZ5RGV Bursitis Approved [12]
Oxazepam DMXNZM4 Alcohol withdrawal delirium Approved [27]
PF-04971729 DM79VXT Type-2 diabetes 5A11 Approved [28]
PITAVASTATIN CALCIUM DM1UJO0 Dyslipidemia 5C80-5C81 Approved [29]
SILODOSIN DMJSBT6 Benign prostatic hyperplasia GA90 Approved [30]
Simvastatin DM30SGU Arteriosclerosis BD40 Approved [23]
Tamoxifen DMLB0EZ Breast cancer 2C60-2C65 Approved [31]
Tapentadol hydrochloride DMXLSH3 Acute pain MG31 Approved [32]
Troglitazone DM3VFPD Diabetic complication 5A2Y Approved [33]
Valproate DMCFE9I Epilepsy 8A60-8A68 Approved [22]
Vorinostat DMWMPD4 Adult acute monocytic leukemia Approved [34]
Zidovudine DM4KI7O Human immunodeficiency virus infection 1C62 Approved [35]
Acemetacin DML6CN4 N. A. N. A. Phase 4 [36]
Dihydrocodeine DMB0FWL Allergic rhinitis CA08.0 Phase 4 [37]
Zaltoprofen DM9RJH7 N. A. N. A. Phase 4 [12]
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⏷ Show the Full List of 46 Approved Drug(s)
8 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
CS-600G DM1PV4Y N. A. N. A. Phase 3 [38]
Dabigatran etexilate DMRDZ4X Venous thromboembolism BD72 Phase 3 [39]
LCQ908 DMFLJHQ Familial chylomicronemia syndrome 5C80 Phase 3 [40]
Rivoglitazone DMBY31K Ocular inflammation 9C61.24 Phase 3 [41]
Bevirimat DML2D8Q Human immunodeficiency virus infection 1C62 Phase 2 [42]
Lersivirine DMSEVBH Human immunodeficiency virus infection 1C62 Phase 2 [43]
Vadimezan DMK7CYX Solid tumour/cancer 2A00-2F9Z Phase 2 [44]
SALVINORIN A DMJ3HQY Cerebral vasospasm BA85.Z Phase 1 [45]
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⏷ Show the Full List of 8 Clinical Trial Drug(s)
2 Investigative Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Alpha-dihydroaldosterone DM6ZTOW N. A. N. A. Investigative [2]
Tetrahydroaldosterone DM2QKOU N. A. N. A. Investigative [2]
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Molecule Interaction Atlas

References

1 Product characteristics of Triumeq.
2 Human uridine diphosphate-glucuronosyltransferase UGT2B7 conjugates mineralocorticoid and glucocorticoid metabolites. Endocrinology. 2003 Jun;144(6):2659-68.
3 Clinical pharmacokinetics and drug-drug interactions of endothelin receptor antagonists in pulmonary arterial hypertension. J Clin Pharmacol. 2012 Dec;52(12):1784-805.
4 In vitro and in vivo oxidative metabolism and glucuronidation of anastrozole. Br J Clin Pharmacol. 2010 Dec;70(6):854-69.
5 Metabolite profiling and reaction phenotyping for the in vitro assessment of the bioactivation of bromfenac. Chem Res Toxicol. 2020 Jan 21;33(1):249-257.
6 Association of carbamazepine major metabolism and transport pathway gene polymorphisms and pharmacokinetics in patients with epilepsy. Pharmacogenomics. 2013 Jan;14(1):35-45.
7 Enantioselective inhibition of carprofen towards UDP-glucuronosyltransferase (UGT) 2B7. Chirality. 2015 Mar;27(3):189-93.
8 Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios. Drug Metab Dispos. 2004 Nov;32(11):1201-8.
9 FDA label of Cenobamate. The 2020 official website of the U.S. Food and Drug Administration.
10 Human UGT2B7 catalyzes morphine glucuronidation. Drug Metab Dispos. 1997 Jan;25(1):1-4.
11 Clinical pharmacokinetics and pharmacodynamics of dapagliflozin, a selective inhibitor of sodium-glucose co-transporter type 2. Clin Pharmacokinet. 2014 Jan;53(1):17-27.
12 Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development. Curr Med Chem. 2009;16(27):3480-675.
13 Eurartesim - European Medicines Agency
14 Empagliflozin (Jardiance): a novel SGLT2 inhibitor for the treatment of type-2 diabetes. P T. 2015 Jun;40(6):364-8.
15 Epirubicin glucuronidation and UGT2B7 developmental expression. Drug Metab Dispos. 2006 Dec;34(12):2097-101.
16 Ezetimibe: a review of its metabolism, pharmacokinetics and drug interactions. Clin Pharmacokinet. 2005;44(5):467-94.
17 The UDP-glucuronosyltransferase 2B7 isozyme is responsible for gemfibrozil glucuronidation in the human liver. Drug Metab Dispos. 2007 Nov;35(11):2040-4.
18 Opioid therapies and cytochrome p450 interactions. J Pain Symptom Manage. 2012 Dec;44(6 Suppl):S4-14.
19 Contribution of UDP-glucuronosyltransferases 1A9 and 2B7 to the glucuronidation of indomethacin in the human liver. Eur J Clin Pharmacol. 2007 Mar;63(3):289-96.
20 Body weight, gender and pregnancy affect enantiomer-specific ketorolac pharmacokinetics. Br J Clin Pharmacol. 2017 Sep;83(9):1966-1975.
21 Regulation of UDP-glucuronosyltransferase (UGT) 1A1 by progesterone and its impact on labetalol elimination. Xenobiotica. 2008 Jan;38(1):62-75.
22 Pharmacokinetic and pharmacodynamic interaction of lorazepam and valproic acid in relation to UGT2B7 genetic polymorphism in healthy subjects. Clin Pharmacol Ther. 2008 Apr;83(4):595-600.
23 Pharmacogenomics of statins: understanding susceptibility to adverse effects. Pharmgenomics Pers Med. 2016 Oct 3;9:97-106.
24 Molecular cloning of the baboon UDP-glucuronosyltransferase 2B gene family and their activity in conjugating morphine. Drug Metab Dispos. 2010 Apr;38(4):545-53.
25 PharmGKB summary: mycophenolic acid pathway. Pharmacogenet Genomics. 2014 Jan;24(1):73-9.
26 Diabetes mellitus reduces activity of human UDP-glucuronosyltransferase 2B7 in liver and kidney leading to decreased formation of mycophenolic acid acyl-glucuronide metabolite. Drug Metab Dispos. 2011 Mar;39(3):448-55.
27 Stereoselective conjugation of oxazepam by human UDP-glucuronosyltransferases (UGTs): S-oxazepam is glucuronidated by UGT2B15, while R-oxazepam is glucuronidated by UGT2B7 and UGT1A9. Drug Metab Dispos. 2002 Nov;30(11):1257-65.
28 The effect of renal impairment on the pharmacokinetics and pharmacodynamics of ertugliflozin in subjects with type 2 diabetes mellitus. J Clin Pharmacol. 2017 Nov;57(11):1432-1443.
29 Pitavastatin: a review in hypercholesterolemia. Am J Cardiovasc Drugs. 2017 Apr;17(2):157-168.
30 Pharmacokinetics and disposition of silodosin (KMD-3213). Yakugaku Zasshi. 2006 Mar;126 Spec no.:237-45.
31 Metabolism and transport of tamoxifen in relation to its effectiveness: new perspectives on an ongoing controversy. Future Oncol. 2014 Jan;10(1):107-22.
32 Investigations into the drug-drug interaction potential of tapentadol in human liver microsomes and fresh human hepatocytes. Drug Metab Lett. 2008 Jan;2(1):67-75.
33 Troglitazone glucuronidation in human liver and intestine microsomes: high catalytic activity of UGT1A8 and UGT1A10. Drug Metab Dispos. 2002 Dec;30(12):1462-9.
34 Age-dependent hepatic UDP-glucuronosyltransferase gene expression and activity in children. Front Pharmacol. 2016 Nov 16;7:437.
35 Determination of UDP-glucuronosyltransferase UGT2B7 activity in human liver microsomes by ultra-performance liquid chromatography with MS detection. J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Jul 1;870(1):84-90.
36 Seyffart G. (1992). Drug dosage in renal insufficiency (2nd ed.). Springer Science+Business Media Dordrecht.
37 Adult and infant pharmacokinetic profiling of dihydrocodeine using physiologically based pharmacokinetic modeling. Biopharm Drug Dispos. 2019 Nov;40(9):350-357.
38 Exploring the metabolism of loxoprofen in liver microsomes: the role of cytochrome P450 and UDP-glucuronosyltransferase in its biotransformation. Pharmaceutics. 2018 Aug 2;10(3). pii: E112.
39 Dabigatran acylglucuronide, the major human metabolite of dabigatran: in vitro formation, stability, and pharmacological activity. Drug Metab Dispos. 2010 Sep;38(9):1567-75.
40 Pradigastat disposition in humans: in vivo and in vitro investigations. Xenobiotica. 2017 Dec;47(12):1077-1089.
41 In vitro metabolism of rivoglitazone, a novel peroxisome proliferator-activated receptor gama agonist, in rat, monkey, and human liver microsomes and freshly isolated hepatocytes. Drug Metab Dispos. 2011 Jul;39(7):1311-9.
42 Bevirimat: a novel maturation inhibitor for the treatment of HIV-1 infection. Antivir Chem Chemother. 2008;19(3):107-13.
43 Excretion and metabolism of lersivirine (5-{[3,5-diethyl-1-(2-hydroxyethyl)(3,5-14C2)-1H-pyrazol-4-yl]oxy}benzene-1,3-dicarbonitrile), a next-generation non-nucleoside reverse transcriptase inhibitor, after administration of [14C]Lersivirine to healthy volunteers. Drug Metab Dispos. 2010 May;38(5):789-800.
44 Preclinical factors affecting the interindividual variability in the clearance of the investigational anti-cancer drug 5,6-dimethylxanthenone-4-acetic acid. Biochem Pharmacol. 2003 Jun 1;65(11):1853-65.
45 Evaluation of the transport, in vitro metabolism and pharmacokinetics of Salvinorin A, a potent hallucinogen. Eur J Pharm Biopharm. 2009 Jun;72(2):471-7.