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1164153-22-3

1164153-22-3 Structure

1164153-22-3 Structure
IdentificationBack Directory
[Name]

3-[4-[[[(3-Methylphenyl)amino]carbonyl]amino]-1H-pyrazol-1-yl]-N-(3,4,5-trimethoxyphenyl)-benzamide
[CAS]

1164153-22-3
[Synonyms]

SR-3576
JNK3 Inhibitor XII
SR-3576 >=98% (HPLC)
JNK3 Inhibitor XII, SR-3576
JNK3 Inhibitor XII, SR-3576 - CAS 1164153-22-3 - Calbiochem
3-(5-(3-m-Tolylureido)-1H-indazol-1-yl)-N-(3,4,5-trimethoxyphenyl)benzamide
3-[4-(3-m-Tolyl-ureido)-pyrazol-1-yl]-N-(3,4,5-trimethoxy-phenyl)-benzamide
3-[4-[[[(3-Methylphenyl)amino]carbonyl]amino]-1H-pyrazol-1-yl]-N-(3,4,5-trimethoxyphenyl)-benzamide
[Molecular Formula]

C27H27N5O5
[MDL Number]

MFCD18632556
[MOL File]

1164153-22-3.mol
[Molecular Weight]

501.53
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

DMSO: ≥20mg/mL
[form ]

powder
[color ]

light brown to brown
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 1 month.
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

2933399990
Hazard InformationBack Directory
[Description]

SR-3576 (1164153-22-3) is a potent and selective JNK3 inhibitor. IC50?= 7nM and >2800-fold selective over p38.1?Cell permeable.
[Uses]

SR 3576 is a JNK-3 selective inhibitor.
[General Description]

A cell-permeable pyrazolourea compound that acts as a potent, ATP binding pocket-targeting, and JNK3-selective inhibitor (IC50 = 7 nM), inhibiting JNK1 only at much higher concentrations (IC50 = 170 nM) and exhibiting little activity against p38 even at concentrations as high as 20 μM. Shown to inhibit streptozotocin- (Cat. No. 572201) induced c-jun phosphorylation in INS-1 rat β-pancreatic cells (IC50 = 1.3 μM).
[Biochem/physiol Actions]

SR-3576 is a small molecule inhibitor belonging to aminopyrazole class that selectively inhibits JNK3 with >2800 fold selectively over p38.1
[storage]

Store at -20°C
[References]

1) Kamenecka?et al. (2009),?Structure-activity relationships and X-ray structures describing the selectivity of aminopyrazole inhibitors for c-Jun N-terminal kinase 3 (JNK3) over p38; J. Biol. Chem.,?284?12853
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