TLR2 antagonist-2
TLR2 antagonist-2 is a selective TLR2 antagonist with an IC50 of 0.94 μM. TLR2 antagonist-2 inhibits TLR1/2 and TLR2/6 heterodimers. TLR2 antagonist-2 is applicable to the research of inflammatory diseases.
For research use only. We do not sell to patients.
- Formula: C23H13F3N2O3
- Molecular Weight:422.36
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
IC50 & Target
[1]|
TLR2 0.94 μM (IC50) |
In Vitro
TLR2 antagonist-2 (Compound b1) potently inhibits the Pam3CSK4-induced TLR2 signaling pathway in HEK-Blue hTLR2 cells, with an IC50 value of 0.94 μM[1].
TLR2 antagonist-2 (increasing concentrations; 24 h) selectively inhibits the signaling pathways of TLR1/2 and TLR2/6 heterodimers in THP1-Dual reporter cells, and shows no activity against TLR4 or TLR7/8 signaling pathways[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
-
Molecular Weight 422.36
-
Formula C23H13F3N2O3
-
SMILES
O=C(C1=CC(C2=CC(C=O)=C(O)C(F)=C2)=NC3=CC=CC=C13)NC4=CC=C(F)C=C4F
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
-
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.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)