Regulatory guidelines do not accurately predict tolvaptan and metabolite interactions at BCRP, OATP1B1, and OAT3 transporters
Abstract Tolvaptan (TLV) was US Food and Drug Administration (FDA)‐approved for the indication to slow kidney function decline in adults at risk of rapidly progressing autosomal dominant polycystic kidney disease in 2018. In vitro, TLV was a breast cancer resistance protein (BCRP) inhibitor, whereas...
Main Authors: | Susan E. Shoaf, Patricia Bricmont, Jennifer Repella Gordon |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2021-07-01
|
Series: | Clinical and Translational Science |
Online Access: | https://doi.org/10.1111/cts.13017 |
Similar Items
-
Mechanistic in vitro studies indicate that the clinical drug–drug interactions between protease inhibitors and rosuvastatin are driven by inhibition of intestinal BCRP and hepatic OATP1B1 with minimal contribution from OATP1B3, NTCP and OAT3
by: Robert Elsby, et al.
Published: (2023-04-01) -
Structure of human drug transporters OATP1B1 and OATP1B3
by: Anca-Denise Ciută, et al.
Published: (2023-09-01) -
Differential Preincubation Effects of Nicardipine on OATP1B1- and OATP1B3-Mediated Transport in the Presence and Absence of Protein: Implications in Assessing OATP1B1- and OATP1B3-Mediated Drug–Drug Interactions
by: Ruhul Kayesh, et al.
Published: (2023-03-01) -
Inhibitory Effects of Quercetin and Its Main Methyl, Sulfate, and Glucuronic Acid Conjugates on Cytochrome P450 Enzymes, and on OATP, BCRP and MRP2 Transporters
by: Violetta Mohos, et al.
Published: (2020-07-01) -
Transporters (OATs and OATPs) contribute to illustrate the mechanism of medicinal compatibility of ingredients with different properties in yuanhuzhitong prescription
by: Ze Wang, et al.
Published: (2020-09-01)