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ChemicalBook--->CAS DataBase List--->1854061-19-0

1854061-19-0

1854061-19-0 Structure

1854061-19-0 Structure
IdentificationBack Directory
[Name]

PF-06761281
[CAS]

1854061-19-0
[Synonyms]

PF-06761281
PF-06761281 >=97% (HPLC)
[Molecular Formula]

C13H17NO6
[MOL File]

1854061-19-0.mol
[Molecular Weight]

283.28
Chemical PropertiesBack Directory
[Boiling point ]

469.7±45.0 °C(Predicted)
[density ]

1.358±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[form ]

powder
[pka]

3.37±0.28(Predicted)
[color ]

white to beige
[Water Solubility ]

H2O: 20mg/mL, clear
Safety DataBack Directory
[Symbol(GHS) ]


GHS06
[Signal word ]

Danger
[Hazard statements ]

H301
[Precautionary statements ]

P301+P330+P331+P310
[RIDADR ]

UN 2811 6.1 / PGIII
Hazard InformationBack Directory
[Uses]

PF-06761281 has been used as a SLC13A family inhibitor, in rats to determine its unbound partition coefficient (Kpuu), to estimate its potency as a drug.
[General Description]

PF-06761281 is a small, polar dicarboxylate compound. Its structure is similar to citrate, which is the endogenous substrate of Na+-citrate cotransporter (NaCT). It is a novel, potent inhibitor of SLC13a2/3/5 (solute channel) family, along with selectivity for NaCT.
[Biochem/physiol Actions]

PF-06761281 is an inhibitor of the sodium-coupled citrate transporter (NaCT or SLC13A5), which may be a target for tretment and prevention of metabolic disorders. The SLC13 transporters SLC13A2 (NaDC1), SLC13A3 (NaDC3), and SLC13A5 (NaCT) co-transport di- and tricarboxylates with multiple sodium ions into cells. PF-06761281 inhibits citrate uptake with an IC50 of 740 nM for NaCT in human hepatocytes. PF-06761281 has >25-fold in vitro selectivity for NaCT over NaDC1 and NaDC3 and was inactive in a selectivity panel of 65 targets.
[storage]

Store at -20°C
1854061-19-0 suppliers list
Company Name: Sigma-Aldrich  
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