DC_AC50

CAS No. 497061-48-0

DC_AC50( —— )

Catalog No. M24456 CAS No. 497061-48-0

DC_AC50 is a dual inhibitor of Atox1 and CCS (copper chaperones).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 71 In Stock
2MG 40 In Stock
5MG 65 In Stock
10MG 100 In Stock
25MG 188 In Stock
50MG 290 In Stock
100MG 435 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    DC_AC50
  • Note
    Research use only, not for human use.
  • Brief Description
    DC_AC50 is a dual inhibitor of Atox1 and CCS (copper chaperones).
  • Description
    DC_AC50 is a dual inhibitor of Atox1 and CCS (copper chaperones). Inhibiting intracellular copper chaperones as a means of reducing/preventing acquired chemotherapy resistance.DC_AC50 binding to Atox1 and CCS and reducing cancer cell proliferation and tumour growth.
  • In Vitro
    Cell Viability Assay Cell Line:Canine OSA (Abrams, D1 and human OSA (HOS, MG63) cells.Concentration:0-10 μM.Incubation Time:72 h.Result:Dose-dependently decreased viability of OSA cells.Apoptosis AnalysisCell Line:Abrams and HOS cells.Concentration:1, 3 and 10 μM (10 μM Carboplatin).Incubation Time:24 h.Result:Potentiated carboplatin-induced apoptosis.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    Apoptosis
  • Recptor
    Atox1|CCS|Apoptosis
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    497061-48-0
  • Formula Weight
    424.26
  • Molecular Formula
    C17H12BrF2N3OS
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:10 mM
  • SMILES
    NC1=C(SC2=C1C=C3CCCC3=N2)C(NC4=C(Br)C=C(C=C4F)F)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Jordon M Inkol, et al. Inhibition of copper chaperones sensitizes human and canine osteosarcoma cells to carboplatin chemotherapy. Vet Comp Oncol. 2020 Dec;18(4):559-569.
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