A CCR4 antagonist
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CCR4 Antagonist (hydrochloride)

Item No. 21885

Technical Information
Formal Name
2-[1,4'-bipiperidin]-1'-yl-N-cycloheptyl-6,7-dimethoxy-4-quinazolinamine, dihydrochloride
CAS Number
1784252-84-1
Synonyms
  • C-021
Molecular Formula
C27H41N5O2 • 2HCl
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMSO: 25 mg/mlEthanol: 5 mg/ml
λmax
214, 248 nm
SMILES
COC(C(OC)=C1)=CC2=C1C(NC3CCCCCC3)=NC(N4CCC(N5CCCCC5)CC4)=N2.Cl.Cl
InChi Code
InChI=1S/C27H41N5O2.2ClH/c1-33-24-18-22-23(19-25(24)34-2)29-27(30-26(22)28-20-10-6-3-4-7-11-20)32-16-12-21(13-17-32)31-14-8-5-9-15-31;;/h18-21H,3-17H2,1-2H3,(H,28,29,30);2*1H
InChi Key
GKJKNYQUFAPLOQ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Chemokine (C-C motif) receptor 4 (CCR4) antagonist is an antagonist of CCR4.1 It inhibits activation of CCR4 by chemokine (C-C motif) ligand 22 (CCL22) in a [35S]GTPγS assay and also inhibits chemotaxis in human and mouse CCR4-expressing B300-19 cells (IC50s = 18, 140, and 39 nM, respectively). CCR4 antagonist inhibits microglial activation in the cortex in a mouse model of hepatic encephalopathy induced by the neurotoxin azoxymethane when administered at a dose of 1 mg/kg per day.2 It reduces azoxymethane-induced increases in Il6 and Il1b expression in mouse cortex. CCR4 antagonist reduces mechanical and thermal sensitivity in a mouse model of type I diabetes induced by streptozotocin (Item No. 13104) when administered intrathecally at doses ranging from 10 to 30 µg/animal.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Yokoyama, K., Ishikawa, N., Igarashi, S., et alDiscovery of potent CCR4 antagonists: Synthesis and structure-activity relationship study of 2,4-diaminoquinazolines. Bioorg. Med. Chem. 16(14), 7021-7032 (2008).

    2. McMillin, M., Frampton, G., Thompson, M., et alNeuronal CCL2 is upregulated during hepatic encephalopathy and contributes to microglia activation and neurological decline. J. Neuroinflammation 11, 121 (2014).

    3. Bogacka, J., Ciapała, K., Pawlik, K., et alBlockade of CCR4 diminishes hypersensitivity and enhances opioid analgesia - Evidence from a mouse model of diabetic neuropathy. Neuroscience 441, 77-92 (2020).