C-021

CAS No. 864289-85-0

C-021( C021 )

Catalog No. M16265 CAS No. 864289-85-0

C-021 is a potent and orally bioavailable CCR4 antagonist with IC50 of 0.14 uM and 0.039 uM for inhibition of chemotaxis in human and mouse, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 92 In Stock
2MG 62 In Stock
5MG 92 In Stock
10MG 147 In Stock
25MG 302 In Stock
50MG 458 In Stock
100MG 642 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    C-021
  • Note
    Research use only, not for human use.
  • Brief Description
    C-021 is a potent and orally bioavailable CCR4 antagonist with IC50 of 0.14 uM and 0.039 uM for inhibition of chemotaxis in human and mouse, respectively.
  • Description
    C-021 is a potent and orally bioavailable CCR4 antagonist with IC50 of 0.14 uM and 0.039 uM for inhibition of chemotaxis in human and mouse, respectively.
  • In Vitro
    ——
  • In Vivo
    Animal Model:Male C57Bl/6 mice (20-25 g) with acute liver failure.Dosage:1 mg/kg Administration:i.p.; daily; for 3 days Result:Significantly less microgliosis, and significantly reduced the pERK1/2 to tERK1/2 ratio.
  • Synonyms
    C021
  • Pathway
    GPCR/G Protein
  • Target
    Chemokine Receptor
  • Recptor
    Chemokine Receptor
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    864289-85-0
  • Formula Weight
    467.658
  • Molecular Formula
    C27H41N5O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 50 mg/mL (106.92 mM)
  • SMILES
    COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCC(CC3)N4CCCCC4)NC5CCCCCC5)OC
  • Chemical Name
    2-([1,4'-bipiperidin]-1'-yl)-N-cycloheptyl-6,7-dimethoxyquinazolin-4-amine

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Yokoyama K, et al. Bioorg Med Chem. 2009 Jan 1;17(1):64-73.
molnova catalog
related products
  • SX-576

    A potent, equipotent CXCR1 and CXCR2 antagonist with IC50 of 31 nM and 21 nM, respectively.

  • GSK812397

    GSK812397 is a potent, selective, noncompetitive, orally available antagonist of CXCR4 receptor.

  • RAMX3

    A tritium-labeled allosteric modulator of the human chemokine receptor CXCR3 with Kd of 1.08 nM.