BiochemProbe — Life Science Research Reagents

NIK SMI1 free base

NIK SMI1 is a highly potent and selective NF-κB-inducing kinase inhibitor.

For research use only. Not for human or veterinary use.

Target NF-κB
Research area Inflammation/Immunology
Purity >98% Stock Inquire

NIK SMI1 structure

CAS No.: 1660114-31-7

Download structure (.mol)

Pack sizes & pricing

Size Price SKU Stock
100 mg USD 600.00 BP-02148-100mg In stock Get quote
250 mg USD 1,150.00 BP-02148-250mg In stock Get quote
500 mg USD 1,800.00 BP-02148-500mg In stock Get quote
1 g USD 2,800.00 BP-02148-1g In stock Get quote

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Description

NIK SMI1 is a highly potent and selective NF-κB-inducing kinase (NIK) inhibitor with Ki of 0.23 nM for NIK-catalyzed hydrolysis of ATP to ADP.

Biological activity

In Vitro NIK SMI1 (Compound 4f) inhibits NIK-catalyzed hydrolysis of ATP to ADP (fluorescence polarization, FP) with an IC50 of 0.23±0.17 nM. NIK SMI1 inhibits the expression of NIK SMI1 response elementregulated firefly luciferase reporter gene in HEK293 cells with an IC50 of 34±6 nM. Consistent with expectations for a NIK inhibitor, NIK SMI1 is shown to inhibit nuclear translocation of p52 (RelB) (IC50=70 nM). NIK SMI1 inhibits BAFF-induced B cell (mouse) survival in vitro with an IC50 of 373±64 nM. n Vivo C57BL/6 mice are treated twice daily for 7 days with orally administered NIK SMI1 or with three injections of recombinant BAFF receptor fusion protein (Br3- mIgG2a) over the course of the 7-day experiment as a positive control. The nonlinearity of exposure relative to dose between 100 and 200 mg/kg is a result of saturation of clearance mechanisms. The pharmacology of NIK SMI1 is examined in SD rat, CD-1 mouse, beagle, and cynomologous monkey with 20, 32, 18, and 7.8 mL/kg per min, respectively. Volume of distribution (Vd, L/kg) is 1.35, 1.58, 0.778, and 1.39, respectively.

Identifiers

SMILES
O=C(N)C1=NC(C2=CC=CC(C#C[C@]3(O)CCN(C)C3=O)=C2)=CC(OC)=C1
InChIKey
LQSHXYHWYGKAMX-FQEVSTJZSA-N

Specifications

MW (average)
365.3826
Formula
C20H19N3O4
CAS No.
1660114-31-7
Physical state
Solid
Color
off-white to pink
Shipping
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage
Powder 4℃ 2 years; In solvent -20℃ 1 month;

Solubility

Soluble in DMSO

References

[1]. Blaquiere N, et al. Scaffold-Hopping Approach To Discover Potent, Selective, and Efficacious Inhibitors of NF-κB Inducing Kinase. J Med Chem. 2018 Aug 9;61(15):6801-6813.

Same target

Search NF-κB

Same research area

Search Inflammation/Immunology

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