MRT199665

TargetMol
Product Code: TAR-T16142
Supplier: TargetMol
CodeSizePrice
TAR-T16142-5mg5mg£458.00
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TAR-T16142-50mg50mg£1,661.00
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Quantity:
TAR-T16142-100mg100mg£2,079.00
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
MRT199665 is an effective and ATP-competitive, selective MARK/SIK/AMPK inhibitor (IC50s of 2/2/3/2 nM, 10/10 nM, and 110/12/43 nM for MARK1/MARK2/MARK3/MARK14, AMPKα1/AMPKα2, and SIK1/SIK2/SIK3, respectively). MRT199665 suppresses the phosphorylation of SIK substrate CRTC3 at S370. MRT199665 induces apoptosis in MEF2C-activated human acute myeloid leukemia (AML) cells.
CAS:
1456858-57-3
Formula:
C28H31N5O2
Molecular Weight:
469.589
Purity:
0.98
SMILES:
CC1(C)C(=O)N([C@H]2CCc3c2cccc3O)c2nc(Nc3cccc(CN4CCCC4)c3)ncc12

References

1. Clark K, et al. Phosphorylation of CRTC3 by the salt-inducible kinases controls the interconversion of classically activated and regulatory macrophages. Proc Natl Acad Sci U S A. 2012 Oct 16;109(42):16986-91. 2. Brown FC, et al. MEF2C Phosphorylation Is Required for Chemotherapy Resistance in Acute Myeloid Leukemia. Cancer Discov. 2018 Apr;8(4):478-497. 3. Hutchinson LD, et al. Salt-inducible kinases (SIKs) regulate TGF?-mediated transcriptional and apoptotic responses.Cell Death Dis. 2020 Jan 22;11(1):49.