SB2960
SB2960 is a receptor for activated protein C kinase 1 (RACK1) binder with a human KD of 5.65 μM. SB2960 can promote stress granule (SG) formation and exhibit potent antiviral activity across diverse viral species. SB2960 suppresses viral replication with minimal cytotoxicity by modulating host antiviral immune responses. SB2960 increases the thermal stability of RACK1 and reduces SARS-CoV-2 N protein levels. SB2960 enhances type I interferon (IFN-β) expression and inhibits RIG-I, ISG56, and RANTES expression. SB2960 can be used for the research of virus infection.
For research use only. We do not sell to patients.
- CAS No.: 3111225-79-4
- Formula: C34H31F3N8O3
- Molecular Weight:656.66
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
RACK1 |
SARS-CoV-2 |
In Vitro
SB2960 (1.2-100 μM) induces stress granule formation in Vero cells with an EC50 of 12.31 μM and reduces SARS-CoV-2 N protein levels in a dose-dependent manner[1].
SB2960 (0.2-100 μM) demonstrates broad-spectrum antiviral activity against multiple RNA viruses in Vero, Calu-3, and Huh7 cells with IC50 values between 3.01 and 5.45 μM[1].
SB2960 (20 μM; 24 h) modulates antiviral gene expression in G3BP1-GFP U-2 OS cells treated with poly(I:C)[1].
SB2960 (0-30 μM) synergizes with Remdesivir (HY-104077) and Nirmatrelvir (HY-138687) against SARS-CoV-2 in Vero cells with high ZIP synergy scores[1].
SB2960 (0.39-700 μM; 24 h) exhibits low cytotoxicity in Vero and G3BP1-GFP U-2 OS cells with a CC50 > 100 μM[1].
SB2960 (20 μM; 24 h) increases the thermal stability of RACK1 in Vero and G3BP1-GFP U-2 OS cell[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
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Cell Line:Vero and G3BP1-GFP U-2 OS cells
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Concentration:40 μM (CETSA)
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Incubation Time:2 h (CETSA)
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Result:Increased the thermal stability of RACK1, with a higher melting temperature (Tm) compared to DMSO-treated cells.
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Cell Line:G3BP1-GFP U-2 OS cells
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Concentration:20 μM
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Incubation Time:24 h
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Result:Enhanced IFN-β expression in poly(I:C)-stimulated cells while attenuating RIG-I, ISG56, and RANTES expression.
Chemical Information
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CAS No. 3111225-79-4
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Molecular Weight 656.66
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Formula C34H31F3N8O3
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SMILES
CC1(C)OC2=CC(N3CCN(C(C4=NC=CN4C)=O)CC3)=C(NC(C5=NC=CC=C5)=O)C=C2C6=C1C=NN6C7=CC=C(C(F)(F)F)C=C7
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
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Research Protocol for Infectious Diseases
Infectious-disease experiments test how pathogens interact with host barriers, innate immune receptors, inflammatory signaling, pathogen replication, and tissue injury; pattern-recognition receptors such as TLRs, RIG-I-like receptors, NOD-like receptors, and inflammasomes detect microbial molecules and activate NF-κB, interferon, and cytokine responses. The central hypothesis is that infection severity reflects the balance between pathogen burden and host response: protective inflammation restricts pathogen growth, whereas excessive or mislocalized inflammation contributes to tissue damage and disease phenotype. Unresolved questions include which host pathways are protective versus pathogenic, why some infection models fail to translate to human disease, and which combined readouts best predict clinically relevant infection outcomes.
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RNA extraction experimental
By lysing cells, releasing RNA, and removing impurities such as proteins and DNA, high-purity RNA products are finally obtained. The commonly used traditional method is the guanidine isothiocyanate/phenol/chloroform method (Trizol), which is suitable for a variety of animal materials including animal tissues, microorganisms, cultured cells, etc., and most plant materials.
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Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
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Mammalian live/dead viability and cytotoxicity staining
Live/dead viability and cytotoxicity staining assays are based on the simultaneous detection of intracellular esterase activity in metabolically active (viable) cells and membrane integrity loss in non-viable cells. In commonly used dual-staining approaches, membrane-permeant fluorogenic substrates are converted by intracellular esterases into fluorescent products in live cells, while impermeant DNA-binding dyes selectively enter cells with compromised plasma membranes and label nucleic acids in dead or dying cells, enabling discrimination between viable and non-viable populations by fluorescence microscopy or flow cytometry.
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Cell Viability Determination by MTT Colorimetric Assay
The following protocol uses the MTT colorimetric assay as a classic literature-established method for assessing cell viability/metabolic activity in cultured mammalian cells. MTT[3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] is reduced by metabolically active cells to a colored formazan product; the amount of formazan is quantified spectrophotometrically and provides an indirect measure of metabolically active viable cells. Importantly, MTT reduction reflects cellular oxidoreductase/metabolic activity rather than an absolute direct count of living cells, so changes in cellular metabolism can alter the signal independently of cell number.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)