6 Results for "

IMQ

" in MedChemExpress (MCE) Product Catalog:
Products (6)

6 Results for "IMQ" in MCE Product Catalog:

Cat. No.: HY-157456
CAS No.: 2763831-43-0
Purity:  ≥98.0%
Target:  

RIP kinase

Research Areas:  

Inflammation/Immunology

RIPK1-IN-19 is a selective RIPK1 inhibitor (IC50=15 nM). RIPK1-IN-19 does not show obvious activity against RIPK2, RIPK3, and RIPK4. RIPK1-IN-19 displays potent protective activity in TNFα-induced systemic inflammatory response syndrome (SIRS) model and Imiquimod (IMQ)-induced psoriasis model. RIPK1-IN-19 can be used in research on inflammation and immune system diseases .
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Cat. No.: HY-155244
CAS No.: 3026677-37-9
Purity:  99.85%
Research Areas:  

Inflammation/Immunology

12R-LOX-IN-2 (compound 7b) is an inhibitor of 12R-lipoxygenase (12R-LOX). 12R-LOX-IN-2 inhibits imiquimod (IMQ)-induced hyperproliferation of psoriatic keratinocytes and suppresses colony formation. 12R-LOX-IN-2 also reduced the protein level of Ki67 and the mRNA expression of IL-17A in IMQ-induced cells. 12R-LOX-IN-2 can be used in research into psoriasis and other skin-related inflammatory diseases .
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Cat. No.: HY-155505
CAS No.: 2953023-30-6
Research Areas:  

Inflammation/Immunology

AHR agonist 4 (compound 24e) is an agonist of Aryl hydrocarbon receptor (AHR), assocaited with the immune balance of Th17/22 and Treg cells. AHR agonist 4 serves as a lead compound for anti-psoriasis drug, alleviates imiquimod (IMQ)-induced psoriasis-like skin lesion . AHR agonist 4 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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Cat. No.: HY-161864
CAS No.: 2256751-16-1
Target:  

STAT

Research Areas:  

Inflammation/Immunology

STAT3-IN-29 (Compound B20) is an inhibitor for STAT3. STAT3-IN-29 inhibits the proliferation of HaCaT cell with IC50 of 0.09 µM, ameliorates the IMQ-induced psoriasis in mouse models .
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Cat. No.: HY-175782
SMU-R39 is a TLR7 and TLR8 antagonist with IC50 values of 3.22 μM and 0.24 μM, respectively. SMU-R39 binds to recombinant mTLR7 protein (KD = 2.36 μM) and to recombinant hTLR8 protein (KD = 105 nM). SMU-R39 suppresses downstream NF-κB and MAPK signaling, and reduces secretion/transcription of pro-inflammatory cytokines (TNF-α, IL-1β, IL-6) in PBMCs and THP-1 cells. SMU-R39 demonstrates anti-inflammatory efficacy in Imiquimod (IMQ) (HY-B0180)-induced psoriasis mouse model. SMU-R39 can be used for the study of autoimmune diseases such as psoriasis .
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Cat. No.: HY-189757
CDK8/19-IN-4 is an orally active CDK8/19 inhibitor. CDK8/19-IN-4 directly binds to and inhibits CDK8/Cyclin C, and inhibits CDK19/Cyclin C. The IC50 values of CDK8/19-IN-4 for CDK8, CDK19, CDK7, and CDK6 are 24.5 nM, 38.6 nM, 412.5 nM, and 694.4 nM, respectively, and the Kd for CDK8 is 46.44 nM. CDK8/19-IN-4 promotes Treg differentiation through the STAT1 and TGF-β/Smad signaling pathways, reduces STAT1 phosphorylation and enhances Smad2/3 activation, and inhibits IL-17A/TNF-α-induced keratinocyte proliferation and inflammatory mediator production. CDK8/19-IN-4 alleviates skin inflammation in the IMQ-induced psoriasis-like model. CDK8/19-IN-4 can be used for research on psoriasis .
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