ZINC00881524

CAS No. 557782-81-7

ZINC00881524( ZINC00881524 | ZINC-00881524 | ZINC 00881524 )

Catalog No. M17542 CAS No. 557782-81-7

ZINC00881524 is an effective and specific ROCK inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 27 In Stock
10MG 42 In Stock
25MG 87 In Stock
50MG 132 In Stock
100MG 203 In Stock
500MG 507 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ZINC00881524
  • Note
    Research use only, not for human use.
  • Brief Description
    ZINC00881524 is an effective and specific ROCK inhibitor.
  • Description
    ZINC00881524 is a potent and selective ROCK inhibitor. Clinically, inhibition of ROCK pathway is believed to contribute to some of the cardiovascular benefits of statin therapy that are independent of lipid lowering (ie, pleiotropic effects).
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ZINC00881524 | ZINC-00881524 | ZINC 00881524
  • Pathway
    Membrane Transporter/Ion Channel
  • Target
    Chloride Channel
  • Recptor
    ROCK
  • Research Area
    Others-Field
  • Indication
    ——

Chemical Information

  • CAS Number
    557782-81-7
  • Formula Weight
    380.46
  • Molecular Formula
    C21H20N2O3S
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : ≥ 300 mg/mL; 788.52 mM
  • SMILES
    O=C(Nc1nc2c(CCc3c2cccc3)s1)Cc1ccc(OC)c(OC)c1
  • Chemical Name
    N-(4,5-dihydronaphtho[1,2-d]thiazol-2-yl)-2-(3,4-dimethoxyphenyl)acetamide

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • CLP257

    CLP257 (CLP-257) is a potent, selective K+-Cl- cotransporter KCC2 activator with EC50 of 616 nM.

  • CLP290

    CLP290 (CLP-290) is an orally acirtve small molecule K+-Cl- cotransporter isotype 2 (KCC2) activator, the carbamate prodrug of CLP257.

  • Fenamic acid

    Fenamic acid is a chloride channel blocker that causes renal papillary necrosis in rats. Fenamic acid serves as a parent structure for several nonsteroidal anti-inflammatory drugs (NSAIDs), including flufenamic acid, tolfenamic acid, mefenamic acid, and meclofenamic acid.