CCR8 agonist 2
CCR8 agonist 2 is a selective CCR8 agonist with an EC50 of 0.008 μM. CCR8 agonist 2 activates CCR8+ activity in a humanized graft-versus-host disease mouse model. CCR8 agonist 2 can be used for the research of autoimmune diseases.
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- Formel: C27H27FN4O3
- Molecular Weight:474.53
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Speicherung:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biologische Aktivität
Beschreibung
IC50 & Target
[1]|
CCR8 0.008 μM (EC50) |
In Vitro
CCR8 agonist 2 (Compound 15d) acts as a potent and selective fully human CCR8 agonist in cell-based calcium mobilization assays, with an EC50 of 0.008 μM[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Parmacokinetics
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:NSG mice (JAX #005557)[1]
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Dosage:30 mg/kg; 300 mg/kg
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Administration:i.p.; on day 1 and day 4 post-PBMC infusion
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Result:Increased the frequency of CCR8+ regulatory T (Treg) cells compared to PBS controls.
Elevated per-cell CCR8 median fluorescent intensity (MFI) in Treg cells compared to PBS controls.
Significantly boosted the frequency of CCR8+ cells in CD4+ conventional T cells relative to PBS controls.
Chemical Information
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Molecular Weight 474.53
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Formel C27H27FN4O3
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SMILES
COC1=C(C=CC=C1)OC2=CC(CN3CCC(C4=CN(N=N4)C5=CC=CC=C5F)(CC3)O)=CC=C2
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
Please store the product under the recommended conditions in the Certificate of Analysis.
Protokoll
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How to Choose the Right Model Animal
Choosing the right model animal is a validity-driven decision in which the species, strain, sex, age, genetic background, disease-induction method, outcome measures, and welfare burden must match the scientific question rather than laboratory tradition or convenience. A model should be selected by judging face validity, construct validity, and predictive validity: whether it resembles the human phenotype, whether it reproduces relevant mechanisms, and whether results are likely to predict human biology or treatment response. Animal studies often fail to translate because of species differences, weak disease resemblance, poor experimental design, inadequate reporting, publication bias, and underuse of randomization, blinding, and sample-size justification. Unresolved questions include how to rank competing models objectively, how much human-disease complexity must be reproduced for a given objective, and when non-animal systems such as organoids, ex vivo tissue, or computational models
Reinheit & Dokumentation
Verweise
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)