ChemicalBook--->CAS DataBase List--->1402727-29-0

1402727-29-0

1402727-29-0 Structure

1402727-29-0 Structure
IdentificationBack Directory
[Name]

PE859
[CAS]

1402727-29-0
[Synonyms]

PE859
PE-859; PE 859
AMBZHNVCLPHAKA-NSJFVGFPSA-N
1H-Indole, 6-[(1E)-2-[5-[(1E)-2-[2-methoxy-4-(2-pyridinylmethoxy)phenyl]ethenyl]-1H-pyrazol-3-yl]ethenyl]-
[Molecular Formula]

C28H24N4O2
[MDL Number]

MFCD28411710
[MOL File]

1402727-29-0.mol
[Molecular Weight]

448.52
Chemical PropertiesBack Directory
[Boiling point ]

747.7±60.0 °C(Predicted)
[density ]

1.312±0.06 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 50 mg/mL (111.48 mM);Water : < 0.1 mg/mL (insoluble)
[pka]

13.78±0.10(Predicted)
Hazard InformationBack Directory
[Uses]

6-((E)-2-(3-((E)-2-Methoxy-4-(pyridin-2-ylmethoxy)styryl)-1H-pyrazol-5-yl)vinyl)-1H-indole is a potent tau aggregation inhibitor that functions as a drug for Alzheimer’s disease.
[Enzyme inhibitor]

This orally bioavailable tau aggregation inhibitor (FW = 448.53 g/mol; IUPAC: 3-[(1E)-2-(1H-indol-6-yl)ethenyl]-5-[(1E)-2-[2-methoxy-4-(2- pyridylmethoxy)phenyl]ethenyl]-1H-pyrazole) significantly reduces formation of sarkosyl-insoluble aggregates of Tau, the principal axonal microtubule-associated protein, and prevents onset and progression of the motor dysfunction in JNPL3 Pro-301-Leu-mutated human tau transgenic mice. PE859 also inhibits aggregation of three-repeat Tau, or 3RMBD-Tau (IC50 = 0.81 μM), and four-repeat Tau, or 2N4R-Tau (IC50 = 2.23 μM).
[storage]

Store at -20°C
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