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SR 3677

SIGMA/SML0774 - ≥98% (HPLC)

Synonym: N-[2-[2-(Dimethylamino)ethoxy]-4-(1H-pyrazol-4-yl)phenyl]-2,3-dihydro-1,4-benzodioxin-2-carboxamide.; SR-3677; SR3677

CAS Number: 1072959-67-1
Empirical Formula (Hill Notation): C22H24N4O4
Molecular Weight: 408.45
Linear Formula: C22H24N4O4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SML0774-5MG 5 mg
$0.00
1/EA
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assay ≥98% (HPLC)
color white to light brown
form powder
Quality Level 100 
solubility DMSO: 15 mg/mL, clear
storage temp. 2-8°C
Application: SR 3677 has been used as Rho-associated kinase (ROCK) inhibitor in cardiac reprogramming.
Biochem/physiol Actions: SR-3677 is a very potent, selective ROCK inhibitor, with higher potency against ROCK II (IC50 = 3 nM) than ROCK I (IC50 = 56 nM). In a kinase screening panel, SR-3677 was shown to only have activity against three other kinases (PKA, MRCK and Akt1) all with IC50 values over 1 μM. The compound has nM potency in cell based assays, and is efficacious in an ex-vivo model for increasing aqueous humor outflow in porcine eyes.
Biochem/physiol Actions: SR3677 decreases amyloid precursor protein (sAPPβ) and amyloid-β (Aβ) in a dose-dependent manner. In 5XFAD mouse brain, SR3677 represses the enzymatic activity of β-site APP cleaving enzyme 1 (BACE1). SR3677 has the ability to change the endocytic supply of BACE1 and induce APP traffic to lysosomes.
Features and Benefits: This compound is featured on the PKA & PKG  and PKB/Akt  pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
Packaging: 5, 25 mg in glass bottle
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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