TG100713

CAS No. 925705-73-3

TG100713( TG100713 )

Catalog No. M17665 CAS No. 925705-73-3

TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 31 In Stock
5MG 50 In Stock
10MG 80 In Stock
25MG 160 In Stock
50MG 302 In Stock
100MG 444 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    TG100713
  • Note
    Research use only, not for human use.
  • Brief Description
    TG100713 is a pan-PI3K inhibitor against PI3Kγ, PI3Kδ, PI3Kα and PI3Kβ with IC50 of 50 nM, 24 nM, 165 nM and 215 nM, respectively.
  • Description
    TG100713 is an inhibitor of PI3-kinase (IC50 values are 24, 50, 165 and 215 nM for PI3Kδ, γ, α and β isoforms respectively). Inhibits endothelial cell proliferation.
  • In Vitro
    TG100713 (10 μM; 48 or 72 h) strongly inhibits endothelial cell (EC) proliferation.
  • In Vivo
    ——
  • Synonyms
    TG100713
  • Pathway
    Cell Cycle/DNA Damage
  • Target
    ROCK
  • Recptor
    PI3Kδ , PI3Kγ , PI3Kα , PI3Kβ
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    925705-73-3
  • Formula Weight
    254.25
  • Molecular Formula
    C12H10N6
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 6.41 mg/mL (25.21 mM)
  • SMILES
    C1=CC(=CC(=C1)O)C2=CN=C3C(=N2)C(=NC(=N3)N)N
  • Chemical Name
    3-(2,4-diaminopteridin-6-yl)phenol

Shipping & Storage Information

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

Reference

1. Doukas J et al. Proc Natl Acad Sci U S A, 2006, 103(52), 19866-19871.
molnova catalog
related products
  • Cucurbitacin A

    Cucurbitacin I, cytotoxic triterpenoid sterols isolated from plants, elicits the formation of actin/phospho-myosin II co-aggregates by stimulation of the RhoA/ROCK pathway and inhibition of LIM-Kinase.

  • Y27632

    Y-27632 is a selective ROCK1 (p160ROCK) inhibitor with Ki of 140 nM in a cell-free assay.

  • CLINODISIDE A

    Clinodiside A in rats with one compartment open model into the body, rapid distribution, elimination rate.