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Curcumin

Substrate Information
Inhibitor Information
Clinical Drug-drug Interactions

In Vitro Substrates

No substrate information.


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In Vitro Inhibitors

* denotes drugs that can potentially be used for in vivo (clinical) studies of the designated transporter
Transporter Synonyms Inhibitor IC50 (μM) Ki (μM) Substrate used Cell System Reference
ABCC1 MRP1 Curcumin 15 Ethacrynic acid glutathione MRP1-expressing Sf9 vesicles Wortelboer, 2003
ABCC2 MRP2, cMOAT Curcumin 5 Ethacrynic acid glutathione MRP2-expressing Sf9 vesicles Wortelboer, 2003
ABCG2 BCRP, MXR Curcumin 1.6 0.7 Sulfasalazine BCRP membrane vesicles Kusuhara, 2012

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Clinical Drug-Drug Interactions

DDI Implicated Transporter* Interacting Drug Affected Drug AUC Cmax CLR CL/F t1/2 Effect on PD Reference More Details
Clinical PK Impact(fold change)
1 ABCG2 Curcumin Sulfasalazine 3.2 3.72 ND 3.24 ND Kusuhara, 2012 DDI 1

PK = pharmacokinetic
The transporters are implicated by in vitro data and/or studies in humans with genetic polymorphisms of the transporter
DDI = Drug Drug Interaction
PD = pharmacodynamic
ND = not determined
NS = not significant
N/A = information not available
Calculation of Fold Change: fold change in the presence of the interacting drug = (value with interacting drug)/(value without interacting drug)
fold change > 1: increase in pharmacokinetic value
fold change < 1: decrease in pharmacokinetic value


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