Home   >  
∨

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

NFκB

Chemical Structure Cat. No. Product Name CAS No.
Shikonin Chemical Structure
 BCP29329 Shikonin 517-89-5
Shikonin is a major component of a Chinese herbal medicine named zicao. Shikonin has shown various biological activities, including inhibition of TNF-α, NF-κB, HIV-1.
Eleutheroside E Chemical Structure
 BCP15731 Eleutheroside E 39432-56-9
Eleutheroside E has anti-inflammatory effect by inhibiting NF-κB activities.
Ginsenoside-Rg5 Chemical Structure
 BCP10278 Ginsenoside-Rg5 186763-78-0
Ginsenoside Rg5 is a triterpenoid saponin. It has a role as a metabolite.
Rocaglamide Chemical Structure
 BCP30539 Rocaglamide 84573-16-0
Rocaglamide is a potent NF-κB activation inhibitor.
H-ALA-ALA-VAL-ALA-LEU-LEU-PRO-ALA-VAL-LEU-LEU-ALA-LEU-LEU-ALA-PRO-VAL-GLN-ARG-LYS-ARG-GLN-LYS-LEU-MET-PRO-OH Chemical Structure
 BCP30335 H-ALA-ALA-VAL-ALA-LEU-LEU-PRO-ALA-VAL-LEU-LEU-ALA-LEU-LEU-ALA-PRO-VAL-GLN-ARG-LYS-ARG-GLN-LYS-LEU-MET-PRO-OH 213546-53-3
SN50 is a cell permeable inhibitor of NF-κB translocation.
Ezetimibe Ketone Chemical Structure
 BCP09273 Ezetimibe Ketone 191330-56-0
Ezetimibe Ketone is Phase-I metabolite of Ezetimibe.
DL-Thioctic acid Chemical Structure
 BCP13221 DL-Thioctic acid 1077-28-7
Alpha-Lipoic Acid is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid inhibits NF-κB-dependent HIV-1 LTR activation.
Naringin Dihydrochalcone Chemical Structure
 BCP27691 Naringin Dihydrochalcone 18916-17-1
Naringin Dihydrochalcone(Naringin DC) is a new-style sweetening agent and an artificial sweetener derived from naringin and also an inhibitor of CYP enzymes.
DH404 Chemical Structure
 BCP30092 DH404 DH404
Dihydro-CDDO-trifluoroethyl amide (dh404) is a novel Nrf2 activator and suppresses oxidative stress in cardiomyocytes.
HG6-64-1 Chemical Structure
 BCP11080 HG6-64-1 1315329-43-1
HG6-64-1 is a potent and selective B-Raf and mutant B-Raf inhibitor.HG6-64-1 is a potent dual TAK1 and MAP4K2 ((germinal center kinase, GCK)) inhibitor with IC50 of 41 nM and 98 nM, respectively.
123下一页末页共 77 条记录 1 / 8 页 
0086-15971444841