CL097
CAS No. 1026249-18-2
CL097 ( —— )
Catalog No. M28181 CAS No. 1026249-18-2
CL097 is an effective agonist of TLR7 and TLR8. CL097 induces pro-inflammatory cytokines in macrophages and NADPH oxidase priming, thereby increasing the fMLF-stimulated ROS production.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 222 | Get Quote |
|
10MG | 335 | Get Quote |
|
25MG | 566 | Get Quote |
|
50MG | 806 | Get Quote |
|
100MG | 1098 | Get Quote |
|
500MG | 2205 | Get Quote |
|
1G | Get Quote | Get Quote |
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Biological Information
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Product NameCL097
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NoteResearch use only, not for human use.
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Brief DescriptionCL097 is an effective agonist of TLR7 and TLR8. CL097 induces pro-inflammatory cytokines in macrophages and NADPH oxidase priming, thereby increasing the fMLF-stimulated ROS production.
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DescriptionCL097 is an effective agonist of TLR7 and TLR8. CL097 induces pro-inflammatory cytokines in macrophages and NADPH oxidase priming, thereby increasing the fMLF-stimulated ROS production.(In Vitro):CL097 (0, 0.5, 2.5, 5, and 10 μg/mL) induces hyperactivation of the NADPH oxidase by stimulating the phosphorylation of p47phox on selective sites in human neutrophils. CL097 (0.1 μM) induces activation of NF-κB in TLR7-transfected HEK293 cells and at 4 μM in TLR8-transfected HEK293 cells.(In Vivo):in NOD mice, CL097 (5 mg/kg, s.c.) causes a modest specific lysis of the target peptide (~25%). However, treatment with a combination of CL097 and CD40 agonist (10 mg/kg, i.p.) results in an increase of approximately twofold in the specific lysis of the IGRP-peptide-coated targets compared with CL097 treatment alone.
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Synonyms——
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PathwayImmunology/Inflammation
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TargetROS
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Recptor5-LOX
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Research Area——
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Indication——
Chemical Information
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CAS Number1026249-18-2
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Formula Weight242.3
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Molecular FormulaC13H14N4O
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Purity>98% (HPLC)
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Solubility——
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SMILESCCOCC1=NC2=C(N1)C(N)=NC1=C2C=CC=C1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Shang E, et al. Development of 3,5-dinitrobenzoate-based 5-lipoxygenase inhibitors. Bioorg Med Chem. 2014 Apr 15;22(8):2396-402.
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