Anticancer agent 46

CAS No. 2426686-17-9

Anticancer agent 46( —— )

Catalog No. M35479 CAS No. 2426686-17-9

Anticancer agent 46 is a potent anti-cancer agent, showing anti-proliferative activity in cellular assays, with an IC50 of 0.986 μM against MGC803 cells.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
25MG 47 Get Quote
50MG 76 Get Quote
100MG 119 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Anticancer agent 46
  • Note
    Research use only, not for human use.
  • Brief Description
    Anticancer agent 46 is a potent anti-cancer agent, showing anti-proliferative activity in cellular assays, with an IC50 of 0.986 μM against MGC803 cells.
  • Description
    Anticancer agent 46 (compound 2) is a potent anticancer agent. Anticancer agent 46 shows antiproliferative activity with an IC50 of 0.986 μM for MGC803 cells. Anticancer agent 46 has the potential for the research of gastric cancer.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2426686-17-9
  • Formula Weight
    319.81
  • Molecular Formula
    C15H14ClN3OS
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (390.86 mM; Ultrasonic )
  • SMILES
    C(=N\NC(NC1=CC=CC=C1)=S)(\C)/C2=C(O)C=CC(Cl)=C2
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Zhang XH, et al. Thiosemicarbazone-based lead optimization to discover high-efficiency and low-toxicity anti-gastric cancer agents. Eur J Med Chem. 2020 Aug 1;199:112349.?
molnova catalog
related products
  • Lumiflavine

    Lumiflavine inhibits riboflavin uptake. It is produced by the photolysis of vitamin B2.

  • Fluorescein diphosph...

    Fluorescein diphosphate tetraammonium is a fluorescent dye and a fluorescent phosphatase substrate that is hydrolyzed into highly fluorescent fluorescein after interaction with phosphatases.

  • K-604

    K-604 is a potent, selective and competitive ACAT-1 inhibitor with IC50 of 0.45 uM for human ACAT-1, displays 229-fold selectivity over ACAT-2.