ChemicalBook--->CAS DataBase List--->1781882-89-0

1781882-89-0

1781882-89-0 Structure

1781882-89-0 Structure
IdentificationBack Directory
[Name]

MRT67307 2HCl
[CAS]

1781882-89-0
[Synonyms]

MRT67307 2HCl
[Molecular Formula]

C26H37ClN6O2
[MOL File]

1781882-89-0.mol
[Molecular Weight]

501.07
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: 92 mg/mL (198.02 mM);Ethanol: 92 mg/mL (198.02 mM)
[Water Solubility ]

Water: 92 mg/mL (198.02 mM)
Hazard InformationBack Directory
[Uses]

MRT67307 dihydrochloride is a dual inhibitor of the IKKε and TBK-1 with IC50s of 160 and 19 nM, respectively[1]. MRT67307 dihydrochloride also inhibits ULK1 and ULK2 with IC50s of 45 and 38 nM, respectively. MRT67307 dihydrochloride also blocks autophagy in cells[2].
[Biological Activity]

MRT67307 is a potent and dual IKKε and TBK1 inhibitor with IC50 of 160 and 19 nM, respectively. MRT67307 potently inhibits ULK1 and ULK2 and blocks autophagy. In macrophages, MRT67307 prevents the phosphorylation of IRF3 and the production of IFNβ. In wild-type MEFs, MRT67307 enhances the IL-1-stimulated phosphorylation of p105 at Ser933 and RelA at both Ser468 and Ser536, and also enhances IL-1-stimulated activation of NF-κB-dependent gene transcription. [1] MRT67307 increases IL-10 production and suppresses proinflammatory cytokine production via a cAMP response element-Binding protein (CREB)-regulated transcriptional coactivator (CRTC) 3 Dependent Mechanism. [2] In addition, MRT67307 inhibit ULK and block autophagy in MEF cells. [3]
[storage]

Store at -20°C
[References]

[1] Clark K, et al. Biochem J. 2011, 434(1), 93-104. [2] Clark K, et al. Proc Natl Acad Sci U S A. 2012, 109(42), 16986-16991. [3] Petherick KJ, et al. J Biol Chem. 2015, 290(18), 11376-11383.
Spectrum DetailBack Directory
[Spectrum Detail]

MRT67307 2HCl(1781882-89-0)1HNMR
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