BMS-345541
- Product Name
- BMS-345541
- CAS No.
- 547757-23-3
- Chemical Name
- BMS-345541
- Synonyms
- CS-1009;BMS-345541 HCl;BMS345541 (HCl Salt);BMS 345541 (HCl Salt);BMS345541 hydrochloride;BMS-345541 hydrochloride;BMS 345541 hydrochloride;BMS345541 HYDROCHLORIDE; BMS-345541 HYDROCHLORIDE; BMS 345541 HYDROCHLORIDE;N1-(1,8-Dimethylimidazo[1,2-a]quinoxalin-4-yl)ethane-1,2-diamine hydrochloride;N-(1,8-Dimethylimidazo[1,2-a]quinoxalin-4-yl)-1,2-ethanediamine hydrochloride
- CBNumber
- CB2497314
- Molecular Formula
- C14Cl1H18N5
- Formula Weight
- 291.78
- MOL File
- 547757-23-3.mol
BMS-345541 Property
- storage temp.
- 2-8°C
- solubility
- DMSO: 18 mg/mL, soluble
- form
- solid
- color
- White to off-white
- InChIKey
- MIDKPVLYXNLFGZ-UHFFFAOYSA-N
Safety
- WGK Germany
- 3
N-Bromosuccinimide Price
- Product number
- B9935
- Product name
- BMS-345541
- Purity
- ≥98% (HPLC), powder
- Packaging
- 5mg
- Price
- $233
- Updated
- 2024/03/01
- Product number
- B9935
- Product name
- BMS-345541
- Purity
- ≥98% (HPLC), powder
- Packaging
- 25mg
- Price
- $384.4
- Updated
- 2024/03/01
- Product number
- 16667
- Product name
- BMS 345541 (hydrochloride)
- Purity
- ≥98%
- Packaging
- 1mg
- Price
- $44
- Updated
- 2024/03/01
- Product number
- 16667
- Product name
- BMS 345541 (hydrochloride)
- Purity
- ≥98%
- Packaging
- 5mg
- Price
- $172
- Updated
- 2024/03/01
- Product number
- 16667
- Product name
- BMS 345541 (hydrochloride)
- Purity
- ≥98%
- Packaging
- 10mg
- Price
- $278
- Updated
- 2024/03/01
BMS-345541 Chemical Properties,Usage,Production
Uses
BMS-345541 has been used:
- as an IκB kinase (IKK) complex inhibitor to study its effects on the interferon-γ (IFN-γ) production by natural killer (NK) cells
- as an IKK inhibitor to study its effects on the expression of eotaxin and monocyte chemoattractant protein-1 (MCP-1) mRNA in gingival fibroblasts
- as nuclear factor κB (NF-κB) pathway inhibitor to study its effects on tumor necrosis factor α (TNFα) production in human oral squamous carcinoma?cells
Biological Activity
bms-345541 is a highly selective inhibitor of ikk-1 and ikk-2 with ic50 values of 4μm and 0.3μm, respectively [1].bms-345541 is a highly selective inhibitor of ikk that inhibits nf-κb-dependent transcription of pro-inflammatory cytokines both in vitro and in vivo. this specificity is proved in the assay measuring the ikk-2-catalyzed phosphorylation of gst-iκb. in this assay, bms-345541 fails to inhibit other serine/threonine and tyrosine kinases. this selectivity is also evident in cells, only the stimulus-induced phosphorylation of iκb was inhibited by bms-345541 whereas other signal transduction cascades were unaffected [1].since the ikk/ nfκb pathway is important for viability of leukemic cells and is a predictor of relapse in t-all, bms-345541 is tested in some t-all cell lines. it is found that bms-345541 can induce apoptosis and an accumulation of cells in the g2/m phase of the cell cycle. bms-345541 can be used in combination with traditional therapies to overcome resistance to chemotherapeutic agents [2].
Biochem/physiol Actions
BMS-345541 possesses anti-inflammatory properties. It also blocks the nuclear factor κB (NF-κB)-dependent transcription of pro-inflammatory cytokines. BMS-345541 possesses anti-inflammatory activity and plays a role in arresting bone erosion in certain animal models.
storage
Store at -20°C
References
[1] james r. burke, mark a. pattoli, kurt r. gregor, patrick j. brassil, john f. macmaster, kim w. mcintyre, xiaoxia yang, violetta s. iotzova, wendy clarke, joann strnad, yuping qiu and f. christopher zusi. bms-345541 is a highly selective inhibitor of iκb kinase that binds at an allosteric site of the enzyme and blocks nf-κb-dependent transcription in mice. j. biol. chem. 2003, 278:1450-1456.
[2] francesca buontempo, francesca chiarini, daniela bressanin, giovanna tabellini, fraia melchionda, andrea pession, milena fini, luca m. neri, james a. mccubrey and alberto m. martelli. activity of the selective iκb kinase inhibitor bms-345541 against t-cell acute lymphoblastic leukemia. cell cycle. 2012, 11 (13): 2467-2475.
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