Title : The System Profile of Renal Drug Transporters in Tubulointerstitial Fibrosis Model and Consequent Effect on Pharmacokinetics.

Pub. Date : 2022 Jan 21

PMID : 35163972






2 Functional Relationships(s)
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1 In addition, the pharmacokinetics of cimetidine, ganciclovir, and digoxin, which were the classical substrates for OCT2, MATE1 and P-glycoprotein (P-gp), respectively, have been studied. Digoxin ATP binding cassette subfamily B member 1 Homo sapiens
2 In addition, the pharmacokinetics of cimetidine, ganciclovir, and digoxin, which were the classical substrates for OCT2, MATE1 and P-glycoprotein (P-gp), respectively, have been studied. Digoxin ATP binding cassette subfamily B member 1 Homo sapiens