JNK inhibitor
Catalog No. M33-900
Catalog No. | Pack Size | Price (USD) | |
---|---|---|---|
M33-900-10 | 10 mg | $75 | |
M33-900-50 | 50 mg | $270 | |
M33-900-BULK | BULK | Contact Us |
Overview:
Selective inhibitor of c-Jun N-terminal kinase (JNK). Reversibly inhibits JNK1,2 and 3 (IC50=40-90 nM) with >300-fold selectivity against related MAP kinases. Anti-inflammatory activity. Inhibits expression of presenilin-1 and Notch signaling in mouse brain. Cell permeable. Active in vivo.
References:
1. BL Bennett et al. Proc. Natl. Acad. Sci. USA. 2001 98:13681
2. M Rahman et al. Brain Res. 2012 1448:117
CAS Registry Number:
129-56-6
Molecular Formula:
C14H8N2O
Appearance:
Yellow powder
Melting Point:
290oC
Molecular Weight:
110.2
Purity:
>98% (TLC); NMR (Conforms)
Solubilization:
May be dissolved in DMSO (22 mg/ml); or Ethanol (2 mg/ml)
Aliases:
1. Anthra [1-9-cd] pyrazol-6(2H)-one
2. 1,9-Pyrazoloanthrone
Storage and Stability:
Store as supplied at ambient temperature for up to 2 years. Store solutions at -20oC for up to 3 months.
Molecular Structure:
Cancer, Cardiovascular Disease, Cytoplasmic Tyrosine Kinases, Inflammation, JAK/STAT Pathway
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