GW406108X (b)

CAS No. 265098-01-9

GW406108X (b)( —— )

Catalog No. M24176 CAS No. 265098-01-9

GW406108X(Z/E) is a mixture of different configurations of GW406108X, which is an inhibitor of Kinesin-12 and ULK1 .

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 272 In Stock
10MG 408 In Stock
25MG 612 In Stock
50MG 918 In Stock
100MG 1233 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    GW406108X (b)
  • Note
    Research use only, not for human use.
  • Brief Description
    GW406108X(Z/E) is a mixture of different configurations of GW406108X, which is an inhibitor of Kinesin-12 and ULK1 .
  • Description
    GW406108X(Z/E) is a mixture of different configurations of GW406108X, which is an inhibitor of Kinesin-12 and ULK1 .
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Autophagy
  • Target
    Autophagy
  • Recptor
    Kinesin-12| ULK1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    265098-01-9
  • Formula Weight
    400.21
  • Molecular Formula
    C20H11Cl2NO4
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C1NC2=C(C=C(C(C3=CC=CO3)=O)C=C2)C1=CC4=CC(Cl)=C(O)C(Cl)=C4
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Dumas M E , Chen G Y , Kendrick N D , et al. Dual inhibition of Kif15 by oxindole and quinazolinedione chemical probes[J]. Bioorganic & Medicinal Chemistry Letters, 2018, 29(2).
molnova catalog
related products
  • DC661

    DC661 (DC-661) is a novel dimeric chloroquine (CQ) that is capable of deacidifying the lysosome and inhibiting autophagy significantly better than HCQ, targets palmitoyl-protein thioesterase 1 (PPT1).

  • CUR5g

    CUR5g is an autophagy inhibitor that inhibits migration and colony formation in A549 cells and acts through a UVRAG-dependent mechanism by blocking the recruitment of STX17 to autophagosomes.

  • Sulfisoxazole

    Sulfisoxazole, an endothelin receptor antagonist, is a sulfonamide antibacterial with an oxazole substituent.