Home   >  
MAPK Pathway
  >  
JNK

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

JNK

Chemical Structure Cat. No. Product Name CAS No.
DTP3 TFA Chemical Structure
BCP34038 DTP3 TFA DTP3
DTP3 TFA is a potent and selective GADD45β/MKK7 (growth arrest and DNA-damage-inducible β/mitogen-activated protein kinase kinase 7) inhibitor.
AS601245 Chemical Structure
BCP32871 AS601245 345987-15-7
AS601245 is a cell-permeable JNK Inhibitor with IC50s of 150, 220, and 70 nM for three JNK human isoforms (hJNK1, hJNK2, and hJNK3), respectively.
SU 3327 Chemical Structure
BCP32078 SU 3327 40045-50-9
SU 3327 is a selective inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 0.7 μM) with selectivity over p38 MAPK and Akt. SU 3327 inhibits the interaction between JNK and JIP (IC50 = 239 nM).
IQ-1S Chemical Structure
BCP17485 IQ-1S 23146-22-7
IQ-1S is a potent and selective c-Jun N-Terminal Kinase Inhibitor. IQ-1S inhibits murine delayed-type hypersensitivity. IQ-1S is highly specific for JNK and that its neutral form is the most abundant species at physiologic pH.
CC-401 hydrochloride Chemical Structure
BCP25004 CC-401 hydrochloride 1438391-30-0
CC-401 hydrochloride is a potent inhibitor of all three forms of JNK with Ki of 25 to 50 nM.
DB-07268 Chemical Structure
BCP16456 DB-07268 929007-72-7
DB07268 is a potent and selective JNK1 inhibitor with an IC50 value of 9 nM.
CC-401 Chemical Structure
BCP01960 CC-401 395104-30-0
CC-401 is a second generation ATP-competitive anthrapyrazolone c-Jun N terminal kinase (JNK) inhibitor with potential antineoplastic activity.
BI-78D3 Chemical Structure
BCP17200 BI-78D3 883065-90-5
BI 78D3 is a competitive c-Jun N-terminal kinase (JNK) inhibitor with IC50 of 280 nM that displays > 100 fold selectivity over p38α and no activity at mTOR and PI-3K.
AstragalosideIV Chemical Structure
BCP28188 AstragalosideIV 84687-43-4
Astragaloside IV, an active component isolated from Astragalus membranaceus, suppresses the activation of ERK1/2 and JNK, and downregulates matrix metalloproteases (MMP)-2, (MMP)-9 in MDA-MB-231 breast cancer cells.
Tomatidine HCl Chemical Structure
BCP10953 Tomatidine HCl 6192-62-7
Tomatidine acts as an anti-inflammatory agent by blocking NF-κB and JNK signaling.
12下一页共 17 条记录 1 / 2 页 
0086-13720134139