NF-κB
NF-κB is a family of conserved and ubiquitous transcription factors that involved in various biological processes including immunity, inflammation, cell growth, differentiation and apoptosis. It is associated with cancer, chronic inflammation and arthritis etc.
Products Related to NF-κB(336)
- GC733015-Aminosalicylic acid-d3CAS: 1309283-32-6Purity: >99.00%
5-Aminosalicylic acid-d3 is the deuterium labeled 5-Aminosalicylic Acid.
- GC73867Balinatunfib (SAR-441566)CAS: 2248726-53-4Purity: >98.00%
Balinatunfib (SAR-441566) is an orally active inhibitor of TNFR1 signaling.
- GC78965ACT001 hydrochlorideCAS: 1403357-80-1Purity: >98.00%
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent.
- GC79059SAP15 acetatePurity: >98.00%
SAP15 (Synthetic anti-inflammatory peptide 15) acetate is a synthetic anti-inflammatory peptide consisting of 15 amino acids designed from human beta-defensin 3.
- GC79407Anti-Mouse CD20 Antibody (18B12)Purity: >99.00%
Anti-Mouse CD20 Antibody (18B12) is a B cell depleting agent that targets mouse CD20.
- GC79486Bacoside A (mixture)Purity: >98.00%
Bacoside A (mixture) is a mixture composed of Bacoside A3, Bacopaside II, Bacopaside X and Bacopasaponin C.
- GC79676PTPRO-IN-1Purity: >98.00%
PTPRO-IN-1 is a selective, orally active PTPRO inhibitor with an IC 50 of 0.16 μM.
- GC79724CHI3L1-IN-5CAS: 2249043-42-1Purity: >98.50%
CHI3L1-IN-5 (Compound Z17) is a highly selective CHI3L1 inhibitor with a K D value of 6 μM.
- GC79803Paeonolsilate sodiumCAS: 827610-11-7Purity: >98.00%
Paeonolsilate (sodium) can inhibit ox-LDL-induced macrophage foam cell formation and inflammation in atherosclerosis.
- GC798056-MethoxymelleinCAS: 13410-15-6Purity: >99.00%
6-Methoxymellein, a phytoalexin, is a NF-κB inhibitor.
- GC79807RP-182 acetatePurity: >98.50%
RP-182 acetate is a synthetic immunomodulatory peptide that exerts anti-tumor effects by targeting the mannose receptor CD206 ( K d = 8 μM) on the surface of tumor-associated macrophages (TAMs).
- GC79808SAR113945 monopotassiumCAS: 899418-65-6Purity: >98.00%
SAR113945 monopotassium is a highly selective IKK-β inhibitor with an IC 50 value of 0.4 nM.
- GC79811Tat-IKIP (46-60) TFAPurity: >99.50%
Tat-IKIP (46-60) TFA is the trifluoroacetic acid of Tat-IKIP (46-60).
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC73301 | 5-Aminosalicylic acid-d3 | 1309283-32-6 | >99.00% | |
5-Aminosalicylic acid-d3 is the deuterium labeled 5-Aminosalicylic Acid. | ||||
| GC73740 | DCZ5418 | 2883709-99-5 | >99.00% | |
DCZ5418 is an inhibitor of TRIP13. | ||||
| GC73867 | Balinatunfib (SAR-441566) | 2248726-53-4 | >98.00% | |
Balinatunfib (SAR-441566) is an orally active inhibitor of TNFR1 signaling. | ||||
| GC74042 | SpiD3 | 3033533-25-1 | >98.00% | |
SpiD3 is a novel spirocyclic dimer. | ||||
| GC74157 | EN450 | 793719-01-4 | >99.00% | |
EN450 is a cysteine-reactive covalent molecular glue degrader targeting NF-κB. | ||||
| GC78965 | ACT001 hydrochloride | 1403357-80-1 | >98.00% | |
ACT001 (Dimethylaminomicheliolide; DMAMCL) hydrochloride is an orally active, blood-brain barrier-permeable anti-inflammatory and anti-tumor agent. | ||||
| GC78981 | HBS-101 | - | >99.50% | |
HBS-101 is a selectively, orally active, brain-penetrant, Midkine (MDK) inhibitor ( K D = 38.4 nM). | ||||
| GC79059 | SAP15 acetate | - | >98.00% | |
SAP15 (Synthetic anti-inflammatory peptide 15) acetate is a synthetic anti-inflammatory peptide consisting of 15 amino acids designed from human beta-defensin 3. | ||||
| GC79389 | ETI41 | 2773474-99-8 | >98.00% | |
ETI41 is an orally active, selective TLR inhibitor that targets the nucleoside-binding Site I on TLR7 ( IC 50 = 0.63 μM) and TLR9 ( IC 50 = 0.16 μM), sparing surface TLRs (including TLR1/TLR2, TLR2/TLR6, TLR4 and TLR5). | ||||
| GC79390 | ETI60 | 2773475-11-7 | >99.50% | |
ETI60 is an orally active, selective TLR inhibitor that targets the nucleoside-binding Site I on TLR7 ( IC 50 = 0.68 μM) and TLR9 ( IC 50 = 0.12 μM), sparing surface TLRs (including TLR1/TLR2, TLR2/TLR6, TLR4 and TLR5). | ||||
| GC79391 | MyD88-IN-3 | - | >99.00% | |
MyD88-IN-3 is an orally active, selective MyD88 Inhibitor. | ||||
| GC79406 | SMU-Z1 | 2410782-66-8 | >99.00% | |
SMU-Z1 is a TLR1/2 heterodimer agonist with an EC 50 of 4.88 nM. | ||||
| GC79407 | Anti-Mouse CD20 Antibody (18B12) | - | >99.00% | |
Anti-Mouse CD20 Antibody (18B12) is a B cell depleting agent that targets mouse CD20. | ||||
| GC79451 | JP-11646 | 1902983-63-4 | >98.50% | |
JP-11646 is a pan-PIM inhibitor with increased potency against PIM2 ( IC 50 = 0.5 nM). | ||||
| GC79486 | Bacoside A (mixture) | - | >98.00% | |
Bacoside A (mixture) is a mixture composed of Bacoside A3, Bacopaside II, Bacopaside X and Bacopasaponin C. | ||||
| GC79676 | PTPRO-IN-1 | - | >98.00% | |
PTPRO-IN-1 is a selective, orally active PTPRO inhibitor with an IC 50 of 0.16 μM. | ||||
| GC79724 | CHI3L1-IN-5 | 2249043-42-1 | >98.50% | |
CHI3L1-IN-5 (Compound Z17) is a highly selective CHI3L1 inhibitor with a K D value of 6 μM. | ||||
| GC79803 | Paeonolsilate sodium | 827610-11-7 | >98.00% | |
Paeonolsilate (sodium) can inhibit ox-LDL-induced macrophage foam cell formation and inflammation in atherosclerosis. | ||||
| GC79804 | Cupabimod | 297774-48-2 | >91.00% | |
Cupabimod is a decoy oligodeoxynucleotide for transcription factor NF-κB. | ||||
| GC79805 | 6-Methoxymellein | 13410-15-6 | >99.00% | |
6-Methoxymellein, a phytoalexin, is a NF-κB inhibitor. | ||||
| GC79806 | TKL002 | 3098518-95-4 | >98.00% | |
TKL002 is a blood-brain barrier-permeable inhibitor of the CTH/H 2 S/NF-κB/EMT signaling axis. | ||||
| GC79807 | RP-182 acetate | - | >98.50% | |
RP-182 acetate is a synthetic immunomodulatory peptide that exerts anti-tumor effects by targeting the mannose receptor CD206 ( K d = 8 μM) on the surface of tumor-associated macrophages (TAMs). | ||||
| GC79808 | SAR113945 monopotassium | 899418-65-6 | >98.00% | |
SAR113945 monopotassium is a highly selective IKK-β inhibitor with an IC 50 value of 0.4 nM. | ||||
| GC79811 | Tat-IKIP (46-60) TFA | - | >99.50% | |
Tat-IKIP (46-60) TFA is the trifluoroacetic acid of Tat-IKIP (46-60). | ||||
