Aristololactam AII

CAS No. 53948-07-5

Aristololactam AII( ——— )

Catalog No. M38286 CAS No. 53948-07-5

Aristolactam A II is a Aristolactam. Aristolactam a small group of compounds mainly found in the Aristolochiaceae.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 949 In Stock
25MG Get Quote In Stock
50MG Get Quote 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
    Aristololactam AII
  • Note
    Research use only, not for human use.
  • Brief Description
    Aristolactam A II is a Aristolactam. Aristolactam a small group of compounds mainly found in the Aristolochiaceae.
  • Description
    Aristolactam AII has cytotoxic activity, it also shows platelet aggregation inhibitory activity.
  • In Vitro
    ———
  • In Vivo
    ———
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    PAFR
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    53948-07-5
  • Formula Weight
    265.26
  • Molecular Formula
    C16H11NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 11 mg/mL (41.47 mM; ultraphonic; )
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Kumar V, et al. Naturally occurring aristolactams, aristolochic acids and dioxoaporphines and their biological activitiesJ. Natural product reports, 2003, 20(6): 565-583.
molnova catalog
related products
  • Antagonist G

    Antagonist G is a potent vasopressin antagonist. Antagonist G is also a weak antagonist of GRP and Bradykinin. Antagonist G induces AP-1 transcription and sensitizes cells to chemotherapy.

  • TMN355

    TMN355 is a potent chemical inhibitor of cyclophilin A and reduces foam cell formation and cytokine secretion,and is used for atherosclerosis. Silencing cyclophilin A in THP-1 cells and human monocytes using siRNA or chemical inhibitor, TMN355 resulted in decrease in lipid uptake by 65-75% even after exposure to oxidized LDL.

  • Men 10376 TFA

    Men 10376 TFA is an effective and selective tachykinin nk-2 receptor antagonist with a K I value of 4.4 M for the nk-2 receptor in the small intestine of rats.