JNK-IN-8
CAS No. 1410880-22-6
JNK-IN-8( JNK-IN-8 | c-Jun N-terminal Kinase Inhibitor XVI )
Catalog No. M11713 CAS No. 1410880-22-6
JNK-IN-8 is a potent, selective, pan-JNK inhibitor with IC50 of 4.7 nM, 18.7 nM and 1 nM for JNK1, JNK2 and JNK3, respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 35 | In Stock |
|
| 5MG | 63 | In Stock |
|
| 10MG | 110 | In Stock |
|
| 25MG | 196 | In Stock |
|
| 50MG | 327 | In Stock |
|
| 100MG | 482 | In Stock |
|
| 200MG | 685 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameJNK-IN-8
-
NoteResearch use only, not for human use.
-
Brief DescriptionJNK-IN-8 is a potent, selective, pan-JNK inhibitor with IC50 of 4.7 nM, 18.7 nM and 1 nM for JNK1, JNK2 and JNK3, respectively.
-
DescriptionJNK-IN-8 is a potent, selective, pan-JNK inhibitor with IC50 of 4.7 nM, 18.7 nM and 1 nM for JNK1, JNK2 and JNK3, respectively; exhibits exceptional selectivity based upon KinomeScan and enzymatic profiling; inhibits c-Jun phosphorylation in HeLa and A375 cells with EC50 of 486 nM and 338 nM, respectively.
-
In Vitro——
-
In Vivo——
-
SynonymsJNK-IN-8 | c-Jun N-terminal Kinase Inhibitor XVI
-
PathwayMAPK/ERK Signaling
-
TargetJNK
-
RecptorJNK1|JNK2|JNK3|Kit(V559D)|Kit(V559D,T670I)
-
Research AreaInflammation/Immunology
-
Indication——
Chemical Information
-
CAS Number1410880-22-6
-
Formula Weight507.6
-
Molecular FormulaC29H29N7O2
-
Purity>98% (HPLC)
-
SolubilityDMSO: ≥ 35 mg/mL
-
SMILESCN(C/C=C/C(NC1=CC=CC(C(NC2=CC=C(C(C)=C2)NC3=NC=CC(C4=CN=CC=C4)=N3)=O)=C1)=O)C
-
Chemical NameBenzamide, 3-[[4-(dimethylamino)-1-oxo-2-buten-1-yl]amino]-N-[3-methyl-4-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]-
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Zhang T, et al. Chem Biol. 2012 Jan 27;19(1):140-54.
molnova catalog
related products
-
GSK2879552 2HCl
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
-
d-Epigalbacin
d-Epigalbacin is a naturally occurring lignin. d-Epigalbacin is a potent, selective JNKs inhibitor, with IC50s of 1.7 μM, 2.9 μM and 1.74 μM for JNK1, JNK2 and JNK3, respectively.
-
SR-3306
SR-3306 is a highly selective, brain penetrant, potent inhibitor of JNK with IC50 of 67, 283 and 159 nM for JNK1, JNK2 and JNK3.
Cart
sales@molnova.com