IκB/IKK
IKK (IκB kinase) is an enzyme complex that participates in NF-κB signaling pathway. It phosphorylates and inhibits IκB, thus leads to the activation of NF-κB. It is a target for treatment of inflammatory diseases and cancer.
Products Related to IκB/IKK(68)
- GC10933Sodium 4-AminosalicylateCAS: 6018-19-5Purity: >99.50%
Sodium 4-Aminosalicylate (4-Aminosalicylic acid sodium salt dihydrate) is one of the antimycobacterial drugs currently used for multidrug-resistant tuberculosis.
- GC12180IKK-16 (IKK Inhibitor VII)CAS: 873225-46-8Purity: >99.00%
IKK-16 (IKK Inhibitor VII) is a selective IκB kinase (IKK) inhibitor for IKK2, IKK complex and IKK1 with IC50s of 40 nM, 70 nM and 200 nM, respectively.
- GC11751QNZ (EVP4593)CAS: 545380-34-5Purity: >98.00%
QNZ (EVP4593) is a highly potent and selective inhibitor of the nuclear factor κB (NF-κB) signaling pathway with an IC 50 value of 11nM and has anti-inflammatory effects.
- GC12370IKK-16 (hydrochloride)CAS: 1186195-62-9Purity: >98%
IKK-16 (hydrochloride) is a novel, orally active selective inhibitor of IκB kinase (IKK), with IC₅₀ values of 40nM, 70nM, and 200nM against IKK-2, IKK complex, and IKK-1.
- GC12399BMS345541 hydrochlorideCAS: 547757-23-3Purity: >99.50%
BMS345541 hydrochloride is an orally active and highly selective inhibitor of IκB kinase (IKK). BMS345541 hydrochloride inhibits IKK-2 (IC 50 =0.3μM) and IKK-1 (IC 50 =4μM).
- GC13035Bay 11-7821CAS: 19542-67-7Purity: >95.00%
Bay 11-7821 is an inhibitor of IκBα phosphorylation and NF-κB, selectively and irreversibly inhibits TNF-α-induced IκB-α phosphorylation (IC 50 value is approximately 10μM), and reduces the expression of NF-κB and adhesion molecules. Bay 11-7821 inhibits ubiquitin-specific proteases USP7 and USP21 with IC 50 values of 0.19 and 0.96μM, respectively .
- GC13926BMS-345541CAS: 445430-58-0Purity: >99.50%
BMS-345541(free base) is a selective inhibitor of the catalytic subunits of IKK (IKK-2 IC50=0.3 μM, IKK-1 IC50=4 μM). BMS-345541(free base) binds at an allosteric site of IKK.
- GC14553ResveratrolCAS: 501-36-0Purity: >99.50%
Resveratrol (trans-Resveratrol; SRT501) is a phytoalexin.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC10933 | Sodium 4-Aminosalicylate | 6018-19-5 | >99.50% | |
Sodium 4-Aminosalicylate (4-Aminosalicylic acid sodium salt dihydrate) is one of the antimycobacterial drugs currently used for multidrug-resistant tuberculosis. | ||||
| GC12013 | Sodium salicylate | 54-21-7 | >99.50% | |
NF-κB inhibitor | ||||
| GC12180 | IKK-16 (IKK Inhibitor VII) | 873225-46-8 | >99.00% | |
IKK-16 (IKK Inhibitor VII) is a selective IκB kinase (IKK) inhibitor for IKK2, IKK complex and IKK1 with IC50s of 40 nM, 70 nM and 200 nM, respectively. | ||||
| GC17830 | IMD 0354 | 978-62-1 | >99.50% | |
IKKβ inhibitor | ||||
| GC10093 | LY2409881 | 946518-60-1 | >98.50% | |
LY2409881 is a selective IκB kinase β (IKK2) inhibitor with an IC50 of 30 nM. | ||||
| GC10135 | AZD3264 | 1609281-86-8 | >99.50% | |
IKK2 inhibitor | ||||
| GC10592 | IKK-3 Inhibitor | 862812-98-4 | >98.50% | |
A multi-kinase inhibitor | ||||
| GC11170 | Choline Fenofibrate | 856676-23-8 | >98.00% | |
| GC11508 | IKK-2 inhibitor VIII | 406209-26-5 | >99.50% | |
| GC11751 | QNZ (EVP4593) | 545380-34-5 | >98.00% | |
QNZ (EVP4593) is a highly potent and selective inhibitor of the nuclear factor κB (NF-κB) signaling pathway with an IC 50 value of 11nM and has anti-inflammatory effects. | ||||
| GC12370 | IKK-16 (hydrochloride) | 1186195-62-9 | >98% | |
IKK-16 (hydrochloride) is a novel, orally active selective inhibitor of IκB kinase (IKK), with IC₅₀ values of 40nM, 70nM, and 200nM against IKK-2, IKK complex, and IKK-1. | ||||
| GC12399 | BMS345541 hydrochloride | 547757-23-3 | >99.50% | |
BMS345541 hydrochloride is an orally active and highly selective inhibitor of IκB kinase (IKK). BMS345541 hydrochloride inhibits IKK-2 (IC 50 =0.3μM) and IKK-1 (IC 50 =4μM). | ||||
| GC12609 | PS 1145 dihydrochloride | 1049743-58-9 | >98% | |
IκB kinase (IKK) inhibitor | ||||
| GC13035 | Bay 11-7821 | 19542-67-7 | >95.00% | |
Bay 11-7821 is an inhibitor of IκBα phosphorylation and NF-κB, selectively and irreversibly inhibits TNF-α-induced IκB-α phosphorylation (IC 50 value is approximately 10μM), and reduces the expression of NF-κB and adhesion molecules. Bay 11-7821 inhibits ubiquitin-specific proteases USP7 and USP21 with IC 50 values of 0.19 and 0.96μM, respectively . | ||||
| GC13184 | PF 184 | 1187460-81-6 | >98% | |
PF 184 is a potent inhibitory factor-κB kinase 2 (IKK-2) inhibitor with an IC50 of 37 nM. | ||||
| GC13278 | IKKε-IN-1 | 1292310-49-6 | >98% | |
potent IKKε inhibitor | ||||
| GC13384 | WS6 | 1421227-53-3 | >98.50% | |
inducer of β cell proliferation | ||||
| GC13926 | BMS-345541 | 445430-58-0 | >99.50% | |
BMS-345541(free base) is a selective inhibitor of the catalytic subunits of IKK (IKK-2 IC50=0.3 μM, IKK-1 IC50=4 μM). BMS-345541(free base) binds at an allosteric site of IKK. | ||||
| GC14553 | Resveratrol | 501-36-0 | >99.50% | |
Resveratrol (trans-Resveratrol; SRT501) is a phytoalexin. | ||||
| GC14989 | MLN120B | 783348-36-7 | >99.50% | |
An IKKβ inhibitor | ||||
| GC15083 | Celastrol | 34157-83-0 | >99.50% | |
Celastrol is a proteasome inhibitor with a potent and preferred inhibition of purified 20S proteasome with an IC 50 of 2.5 μM. | ||||
| GC15942 | ML 120B dihydrochloride | - | >98% | |
IKK2-selective inhibitor | ||||
| GC16044 | Emodin | 518-82-1 | >98.00% | |
Emodin is a bioactive anthraquinone with anti-tumor, anti-bacterial, and vasorelaxant effects. | ||||
| GC16303 | Bay 65-1942 HCl salt | 600734-06-3 | >99.00% | |
