An inhibitor of glycogen phosphorylase
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Glycogen Phosphorylase Inhibitor

Item No. 17578

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
2-chloro-4,5-difluoro-N-[[[2-methoxy-5-[[(methylamino)carbonyl]amino]phenyl]amino]carbonyl]-benzamide
CAS Number
648926-15-2
Synonyms
  • GPI
Molecular Formula
C17H15ClF2N4O4
Formula Weight
412.8
Purity
≥98%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 5 mg/mlDMSO: 5 mg/ml
λmax
238, 302 nm
SMILES
FC1=C(F)C=C(C(NC(NC2=C(OC)C=CC(NC(NC)=O)=C2)=O)=O)C(Cl)=C1
InChi Code
InChI=1S/C17H15ClF2N4O4/c1-21-16(26)22-8-3-4-14(28-2)13(5-8)23-17(27)24-15(25)9-6-11(19)12(20)7-10(9)18/h3-7H,1-2H3,(H2,21,22,26)(H2,23,24,25,27)
InChi Key
ROJNYKZWTOHRNU-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $107

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    5 mg

    $451

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    Product Description

    Glycogen phosphorylase inhibitor is a cell-permeable acyl urea first identified as an inhibitor of human liver glycogen phosphorylase (IC50 = 53 nM).1 It blocks glucagon-induced hepatic glycogenolysis in vivo.1 Glycogen phosphorylase inhibitor has been used to study glycogen utilization in human liver HepG2 cells, retinal explants, and human T lymphocyte Kit 225 cells.2,3,4

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Klabunde, T., Wendt, K.U., Kadereit, D., et al. Acyl ureas as human liver glycogen phosphorylase inhibitors for the treatment of type 2 diabetes. J. Med. Chem. 48(20), 6178-6193 (2005).

    2. Cheng, A., Zhang, M., Gentry, M.S., et al. A role for AGL ubiquitination in the glycogen storage disorders of Lafora and Cori’s disease. Genes Dev. 21(19), 2399-2409 (2007).

    3. Agathocleous, M., Love, N.K., Randlett, O., et al. Metabolic differentiation in retinal cells. Nat. Cell Biol. 14(8), 859-864 (2012).

    4. Arrizabalaga, O., Lacerda, H.M., Zubiaga, A.M., et al. Rac1 protein regulates glycogen phosphorylase activation and controls interleukin (IL)-2-dependent T cell proliferation. The Journal of Biological Chemisty 287(15), 11878-11890 (2012).