Amsacrine

CAS No. 51264-14-3

Amsacrine ( —— )

Catalog No. M14772 CAS No. 51264-14-3

Amsacrine (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.

Purity : >98%(HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
10MG 35 In Stock
25MG 52 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Amsacrine
  • Note
    Research use only, not for human use.
  • Brief Description
    Amsacrine (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells.
  • Description
    Amsacrine (mAMSA) an antineoplastic agent which can intercalate into the DNA of tumor cells. Amsacrine also expresses topoisomerase inhibitor activity, specifically inhibiting topoisomerase II.
  • Synonyms
    ——
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    Potassium Channel
  • Recptor
    Potassium Channel; Topo II
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    51264-14-3
  • Formula Weight
    393.46
  • Molecular Formula
    C21H19N3O3S
  • Purity
    >98%(HPLC)
  • Solubility
    DMSO: 9.3 mg/mL
  • SMILES
    COC1=C(NC2=C3C=CC=CC3=NC3=CC=CC=C23)C=CC(NS(C)(=O)=O)=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Thomas D, et al. Br J Pharmacol. 2004 Jun;142(3):485-94.
molnova catalog
related products
  • 2,2,2-Trichloroethan...

    2,2,2-Trichloroethanol is an agonist of the nonclassical K2P channels TREK-1 and TRAAK.

  • Retigabine

    Retigabine (Ezogabine; D23129) is a Kv7.2-7.5 (KCNQ2-5) neuronal potassium channel opener witrh anticonvulsant activity.

  • VU591 hydrochloride

    VU591 hydrochloride is a selective renal outer medullary potassium channel (Kir1.1, ROMK) antagonist (IC50:0.24 μM).?Thought to block the intracellular pore of the Kir1.1 channel.?Exhibits no effect on Kir7.1 at concentrations up to 10 μM;?does not inhibit Kir2.1, Kir2.3 or Kir4.1.?