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BMS345541 hydrochloride Sale

(Synonyms: N-(1,8-二甲基咪唑并[1,2-A]喹喔啉-4-基)-1,2-乙二胺盐酸盐,BMS-345541 hydrochloride;BMS 345541 hydrochloride) 目录号 : GC12399

A selective inhibitor of IKKα and IKKβ

BMS345541 hydrochloride Chemical Structure

Cas No.:547757-23-3

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5mg
¥830.00
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10mg
¥1,145.00
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50mg
¥3,612.00
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Sample solution is provided at 25 µL, 10mM.

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Description

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].

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.

实验参考方法

Kinase experiment [1]:

Enzyme Assays

Assays measuring the enzyme-catalyzed phosphorylation of GST-IκBα were performed by adding enzyme (IKK-2, IKK-1 or IKK-ε, typically to a final concentration of 0.5 μg/mL) at 30℃ to solutions of 100 μg/mL GST- IκBα and 5 μM [33P]ATP in 40 mM Tris HCl, pH 7.5, containing 4 mM MgCl2, 34 mM sodium phosphate, 3 mM NaCl, 0.6 mM potassium phosphate, 1 mM KCl, 1 mM dithiothreitol, 3% (w/v) glycerol, and 250 μg/mL bovine serum albumin. The specific activity of [33P]ATP used in the assay was 100 Ci/mmol. After 5 mins, the kinase reactions were stopped by the addition of 2× Laemmli sample buffer and heat-treated at 90℃ for 1 min. The samples were then loaded on to NuPAGE 10% BisTris gels. After completion of SDS-PAGE, gels were dried on a slab gel dryer. The bands were then detected using a 445Si PhosphorImager, and the radioactivity was quantified using ImageQuant software. Under these conditions, the degree of phosphorylation of GST-IκBα was linear with time and concentration of enzyme.

Cell experiment [1]:

Cell lines

THP-1 monocytic cells

Preparation method

Soluble in DMSO. General tips for obtaining a higher concentration: Please warm the tube at 37℃ for 10 minutes and/or shake it in the ultrasonic bath for a while. Stock solution can be stored below -20℃ for several months.

Reaction Conditions

1 ~ 100 μM or 0.04 ~ 25 μM; 60 mins

Applications

BMS-345541 inhibited the TNFα-stimulated phosphorylation of Iκ-Bα in a dose-dependent manner (IC50 = 4 μM), and reduced the stimulated production of TNFα, IL-1β, IL-8 and IL-6 (IC50 = 1 ~ 5 μM).

Animal experiment [1]:

Animal models

Female BALB/c mice

Dosage form

2 mg/kg (1 mL/kg), i.v.; 10 mg/kg (5 mL/kg), p.o.

Applications

Oral administration of BMS-345541 to mice resulted in prolonged serum drug levels, with concentrations sustained at or above 1 μM for many hrs. BMS-345541 exhibited 100% oral bioavailability. At the dose of 10 mg/kg, BMS-345541 inhibited the production of TNFα induced by LPS and exhibited 50% inhibition. At the dose of 100 mg/kg, BMS-345541 completely inhibited TNFα production.

Other notes

Please test the solubility of all compounds indoor, and the actual solubility may slightly differ with the theoretical value. This is caused by an experimental system error and it is normal.

References:

[1]. Burke JR, Pattoli MA, Gregor KR, et al. BMS-345541 is a highly selective inhibitor of I kappa B kinase that binds at an allosteric site of the enzyme and blocks NF-kappa B-dependent transcription in mice. J Biol Chem, 2003, 278(3): 1450-1456.

化学性质

Cas No. 547757-23-3 SDF
别名 N-(1,8-二甲基咪唑并[1,2-A]喹喔啉-4-基)-1,2-乙二胺盐酸盐,BMS-345541 hydrochloride;BMS 345541 hydrochloride
化学名 N'-(1,8-dimethylimidazo[1,2-a]quinoxalin-4-yl)ethane-1,2-diamine;hydrochloride
Canonical SMILES CC1=CC2=C(C=C1)N=C(C3=NC=C(N23)C)NCCN.Cl
分子式 C14H18ClN5 分子量 291.78
溶解度 ≥ 60 mg/mL in Water 储存条件 Store at 2-8°C
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1 mg 5 mg 10 mg
1 mM 3.4272 mL 17.1362 mL 34.2724 mL
5 mM 0.6854 mL 3.4272 mL 6.8545 mL
10 mM 0.3427 mL 1.7136 mL 3.4272 mL
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