BI01383298 | Citrate transporter inhibitor

CAS:
 2227549-00-8
Catalog Number:
 10-4191
BI01383298 chemical structure Focus Biomolecules

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5 mg$50.00
25 mg$170.00

BI01383298 (2227549-00-8) is a potent, non-competitive, irreversible inhibitor of the human Na+-coupled citrate transporter (NaCT/SLC13A5/mINDY).1,2  IC50 = 49 nM in the presence of Li+ with preincubation and 118 nM without Li+.  BI01393298 is inactive in mouse NaCT for citrate transport.  NaCT delivers citrate, a key metabolite and regulator of multiple biochemical pathways, from the blood to hepatocytes and neurons. BI01383298 also blocked transport of arginine, dimethylarginine, and L-homoarginine in both human and mouse NaCT.2

References/Citations:

  1. Higuchi et al. (2020) Functional analysis of a species-specific inhibitor selective for human Na+-coupled citrate transporter (NaCT/SLC13A5/mINDY); Biochem. J. 477 4149
  2. Surrer et al. (2022) L-Arginine and Cardioactive Arginine Derivatives as Substrates and Inhibitors of Human and Mouse NaCT/Nact; Metabolites 12 273
CAS:
2227549-00-8
Catalog Number:
10-4191
Activity:
SLC13A5 inhibitor
Chemical Names:
1-(3,5-Dichlorophenylsulfonyl)-N-(4-fluorobenzyl)piperidine-4-carboxamide
Molecular Weight:
445.34
Molecular Formula:

C19H19Cl2FN2O3S

Solubility:
Soluble in DMSO (at least 35 mg/ml)
Physical Properties:
White solid
Purity:

>98% by HPLC
NMR: (Conforms)

Storage Temperature:
-20°C
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored under an inert atmosphere at -20°C for up to 3 months.
Shipping Code:
RT

Safety Data Sheet:

N/A

Product Data Sheet:

Materials provided by Focus Biomolecules are for laboratory research use only and are not intended for human or veterinary applications. Please note that we do not sell to individuals and that all orders placed by non-research organizations will incur a $20 restocking/refund fee

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