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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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B275312-5mg | 5mg | In stock | $88.90 | |
B275312-10mg | 10mg | In stock | $137.90 | |
B275312-25mg | 25mg | In stock | $276.90 | |
B275312-50mg | 50mg | In stock | $444.90 | |
B275312-100mg | 100mg | In stock | $801.90 |
Highly selective cell permeable IKK-2 and IKK-1 inhibitor
Synonyms | 445430-58-0 | BMS-345541 | BMS-345541 free base | BMS345541 | N1-(1,8-dimethylimidazo[1,2-a]quinoxalin-4-yl)ethane-1,2-diamine | IKK Inhibitor III, BMS-345541 | IKK Inhibitor III | BMS-345541(free base) | 1,2-Ethanediamine, N-(1,8-dimethylimidazo(1,2-a)quinoxalin-4-yl)- | |
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Specifications & Purity | ≥99% |
Biochemical and Physiological Mechanisms | Highly selective cell permeable IKK-2 and IKK-1 inhibitor (IC 50 values are 0.3 and 4 μM for IKK-2 and IKK-1 respectively). Blocks NF-κB-dependent transcription. Shows anti-inflammatory and radiosensitizing effects in vivo. Orally active. |
Storage Temp | Store at -20°C,Desiccated |
Shipped In | Ice chest + Ice pads |
Note | Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details. |
Product Description | BMS-345541 is a highly selective inhibitor of the catalytic subunits of IKK-2 and IKK-1 with IC50 of 0.3 μM and 4 μM, respectively. |
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IUPAC Name | N'-(1,8-dimethylimidazo[1,2-a]quinoxalin-4-yl)ethane-1,2-diamine |
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INCHI | InChI=1S/C14H17N5/c1-9-3-4-11-12(7-9)19-10(2)8-17-14(19)13(18-11)16-6-5-15/h3-4,7-8H,5-6,15H2,1-2H3,(H,16,18) |
InChi Key | PSPFQEBFYXJZEV-UHFFFAOYSA-N |
Canonical SMILES | CC1=CC2=C(C=C1)N=C(C3=NC=C(N23)C)NCCN |
Isomeric SMILES | CC1=CC2=C(C=C1)N=C(C3=NC=C(N23)C)NCCN |
PubChem CID | 9813758 |
Molecular Weight | 255.32 |
Enter Lot Number to search for COA:
To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
G2208195 | Certificate of Analysis | Jun 07, 2022 | B275312 |
G2208204 | Certificate of Analysis | Jun 07, 2022 | B275312 |
G2208296 | Certificate of Analysis | Jun 07, 2022 | B275312 |
G2208297 | Certificate of Analysis | Jun 07, 2022 | B275312 |
G2208336 | Certificate of Analysis | Jun 07, 2022 | B275312 |
Solubility | Soluble in DMSO to 25 mM |
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1. Mirzaei R et al.. (2021) PD-1 independent of PD-L1 ligation promotes glioblastoma growth through the NF?B pathway.. Sci Adv, 7 (45): (eabh2148). [PMID:34739319] |
2. Hahn A et al.. (2020) Serum amyloid A1 mediates myotube atrophy via Toll-like receptors.. J Cachexia Sarcopenia Muscle, 11 (103-119). [PMID:31441598] |
3. Zhang Y et al.. (2017) The Unknown Aspect of BAFF: Inducing IL-35 Production by a CD5+CD1dhiFc?RIIbhiRegulatory B-Cell Subset in Lupus.. J Invest Dermatol, 137 (12): (2532-2543). [PMID:28844943] |