A TG2 inhibitor
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Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

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BJJF078

Item No. 42397

Technical Information
Formal Name
3,4-dimethoxy-N-[5-[[4-[(1-oxo-2-propen-1-yl)amino]-1-piperidinyl]sulfonyl]-1-naphthalenyl]-benzamide
CAS Number
2531244-56-9
Molecular Formula
C27H29N3O6S
Formula Weight
Purity
≥98%
A solid
DMSO: Soluble: ≥10 mg/mlEthanol: Sparingly Soluble: 1-10 mg/ml
SMILES
O=C(C1=CC=C(C(OC)=C1)OC)NC2=CC=CC3=C(S(=O)(N4CCC(NC(C=C)=O)CC4)=O)C=CC=C32
InChi Code
InChI=1S/C27H29N3O6S/c1-4-26(31)28-19-13-15-30(16-14-19)37(33,34)25-10-6-7-20-21(25)8-5-9-22(20)29-27(32)18-11-12-23(35-2)24(17-18)36-3/h4-12,17,19H,1,13-16H2,2-3H3,(H,28,31)(H,29,32)
InChi Key
IJRQXDUGUAWTNT-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    BJJF078 is an inhibitor of transglutaminase 2 (TG2; IC50s = 41 and 54 nM for the human and mouse enzymes, respectively).1 It is selective for TG2 over Factor XII (IC50 = 22 µM for the human enzyme) but does inhibit TG1 (IC50 = 0.16 µM for the human enzyme).

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Chrobok, N.L., Bol, J.G.J.M., Jongenelen , C.A., et al. Characterization of transglutaminase 2 activity inhibitors in monocytes in vitro and their effect in a mouse model for multiple sclerosis. PLoS One 13(4), e0196433 (2018).