A negative control compound for GSK-J4
Related Products
Active Metabolite(s)
12056GSK-J2 (sodium salt)
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GSK-J5 (hydrochloride)

Item No. 12074

Technical Information
Formal Name
N-[2-(3-pyridinyl)-6-(1,2,4,5-tetrahydro-3H-3-benzazepin-3-yl)-4-pyrimidinyl]-β-alanine, ethyl ester, monohydrochoride
CAS Number
1797983-32-4
Molecular Formula
C24H27N5O2 • HCl
Formula Weight
Purity
≥95%
Formulation
A crystalline solid
DMF: 30 mg/mlDMF:PBS (pH 7.2) (1:7): 0.1 mg/mlDMSO: 30 mg/mlEthanol: 20 mg/ml
λmax
202, 254 nm
SMILES
O=C(OCC)CCNC1=CC(N2CCC(C=CC=C3)=C3CC2)=NC(C4=CC=CN=C4)=N1.Cl
InChi Code
InChI=1S/C24H27N5O2.ClH/c1-2-31-23(30)9-13-26-21-16-22(28-24(27-21)20-8-5-12-25-17-20)29-14-10-18-6-3-4-7-19(18)11-15-29;/h3-8,12,16-17H,2,9-11,13-15H2,1H3,(H,26,27,28);1H
InChi Key
QQHQMHJAOKADED-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    GSK-J5 is a pyridine regio-isomer of GSK-J4. Like GSK-J4, this isomer is cell-permeable and hydrolyzed to a free base.1 However, the free base is a weak inhibitor of JMJD3 (IC50 > 100 μM), making it an ideal inactive control molecule for elucidating the functional role of JMJD3 inhibition.1 See the Structural Genomics Consortium (SGC) website for more information.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kruidenier, L., Chung, C.W., Cheng, Z., et alA selective jumonji H3K27 demethylase inhibitor modulates the proinflammatory macrophage response. Nature 488(7411), 404-408 (2012).

    Product Citations

    Burgess, S.L., Saleh, M., Cowardin, C.A., et alRole of serum amyloid A, granulocyte-macrophage colony stimulating factor, and bone marrow granulocyte-monocyte precursor expansion in segmented filamentous bacterium-mediated protection from Entamoeba histolytica. Infect. Immun. 84(10), 2824-2832 (2016).