Title : Comparative vulnerability of PET radioligands to partial inhibition of P-glycoprotein at the blood-brain barrier: A criterion of choice?

Pub. Date : 2022 Jan

PMID : 34496661






2 Functional Relationships(s)
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Protein Name
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1 In vitro, the half-maximum inhibitory concentration (IC50) of the potent P-gp inhibitor tariquidar in P-gp-overexpressing cells was significantly different using either (11C)verapamil (44 nM), (11C)N-desmethyl-loperamide (19 nM) or (11C)metoclopramide (4 nM) as substrate probes. tariquidar ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus
2 In vitro, the half-maximum inhibitory concentration (IC50) of the potent P-gp inhibitor tariquidar in P-gp-overexpressing cells was significantly different using either (11C)verapamil (44 nM), (11C)N-desmethyl-loperamide (19 nM) or (11C)metoclopramide (4 nM) as substrate probes. tariquidar ATP-binding cassette, subfamily B (MDR/TAP), member 1B Rattus norvegicus