MD 39-AM

CAS No. 72564-74-0

MD 39-AM( MD-39-AM | MD 39 AM | MD39AM )

Catalog No. M17581 CAS No. 72564-74-0

Anticytokinin activity was evaluated by 50% of the callus growth on the medium with kinetin but without anti-cytokinin

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 34 In Stock
5MG 52 In Stock
10MG 81 In Stock
25MG 195 In Stock
50MG 333 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
    MD 39-AM
  • Note
    Research use only, not for human use.
  • Brief Description
    Anticytokinin activity was evaluated by 50% of the callus growth on the medium with kinetin but without anti-cytokinin
  • Description
    MD-39-AM is a diuretic agent, impling an increase in the Na+ excretion and showing antihypertensive effect.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    MD-39-AM | MD 39 AM | MD39AM
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    ROCK
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    72564-74-0
  • Formula Weight
    268.34
  • Molecular Formula
    C14H12N4S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CSc1nc2c(cccn2)c(n1)Nc1ccccc1
  • Chemical Name
    2-Methylsulfanyl-N-phenylpyrido[2,3-d]pyrimidin-4-amine

Shipping & Storage Information

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

Reference

1. Pérez MJ, et al. Preliminary pharmacokinetics of a new pyridopyrimidine derivative. Arzneimittelforschung. 1991 Jun;41(6):640-4.
molnova catalog
related products
  • Narciclasine

    Narciclasine, a natural product, modulates the Rho/Rho-kinase/LIM kinase/cofilin signaling pathway, greatly increasing GTPase RhoA activity.

  • CKI-7

    CKI-7 2HCl is a potent and ATP-competitive inhibitor of casein kinase 1 (CK1; IC50: 6 μM; Ki: 8.5 μM) and a selective Cdc7 kinase inhibitor.

  • ROCK2-IN-2

    ROCK2-IN-2 is a selective inhibitor of ROCK2 (IC50 of <1 μM).