SW-044248

CAS No. 522650-83-5

SW-044248 ( SW 044248;SW044248 )

Catalog No. M14846 CAS No. 522650-83-5

SW-044248 is a novel selective inhibitor of Topoisomerase I; inhibits Top I differently from camptothecin.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 33 In Stock
5MG 53 In Stock
10MG 87 In Stock
25MG 178 In Stock
50MG 340 In Stock
100MG 511 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    SW-044248
  • Note
    Research use only, not for human use.
  • Brief Description
    SW-044248 is a novel selective inhibitor of Topoisomerase I; inhibits Top I differently from camptothecin.
  • Description
    SW-044248 is a novel selective inhibitor of Topoisomerase I; inhibits Top I differently from camptothecin; selectively toxic for some NSCLC cell lines.Lung Cancer Preclinical
  • Synonyms
    SW 044248;SW044248
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Topoisomerase
  • Recptor
    TopoI
  • Research Area
    Cancer
  • Indication
    Lung Cancer

Chemical Information

  • CAS Number
    522650-83-5
  • Formula Weight
    421.52
  • Molecular Formula
    C22H23N5O2S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: ≥ 30 mg/mL
  • SMILES
    CCN1C2=CC=CC=C2C3=C1N=C(N=N3)SC(C(NC4=CC=CC=C4OC)=O)CC
  • Chemical Name
    Butanamide, 2-[(5-ethyl-5H-1,2,4-triazino[5,6-b]indol-3-yl)thio]-N-(2-methoxyphenyl)-

Shipping & Storage Information

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

Reference

1. Zubovych IO, et al. Mol Cancer Ther. 2016 Jan;15(1):23-36.
2. Kim HS, et al. Cell. 2013 Oct 24;155(3):552-66.
molnova catalog
related products
  • 10-Hydroxycamptothec...

    (S)-10-Hydroxycamptothecin is a clinical therapy agent against hepatoma.

  • Voreloxin

    A first-in-class anticancer quinolone derivative that intercalates DNA and inhibits Topoisomerase II.

  • Proscillaridin A

    Proscillaridin A is a natural product.It is a potent poison of topoisomerase I/II activity with IC50 values of 30 nM and 100 nM, respectively.