HG-9-91-01

    • Catalog No.:MC1374
    • Description
    • CasNo:
    • 1456858-58-4
    • MolecularFormula:
    • C32H37N7O3
    • Purity:
    • >98%
    • Target:
    • Salt-inducible Kinase (SIK)
    • IC50:
    • IC50: 0.92/6.6/9.6 nM (SIK1/2/3)[1]
    • In Vitro:
    • HG-9-91-01 inhibits a number of protein tyrosine kinases that possess a threonine residue at the gat
    • Fields:
    • HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIKs) inhibitor with IC50s of 0.9
    • Specificity:
    • Target: Salt-inducible Kinase (SIK). Fields: HG-9-91-01 is a potent and highly selective salt-inducible kinase (SIKs) inhibitor with IC50s of 0.92 nM, 6.6 nM and 9.6 nM for SIK1, SIK2 and SIK3 respect
    • Dilution:
    • IC50: 0.92/6.6/9.6 nM (SIK1/2/3)[1]
    • Concentration:
    • >98%
    • Storage Stability:
    • 2 years -20°C Powder, 2 weeks4°C in DMSO,6 months-80°C in DMSO
    • Other Name:
    • SIK inhibitor 1
    • MolecularWeight(Da):
    • 567.6799999999999
    • References:
    • [1]. Clark K, et al. Phosphorylation of CRTC3 by the salt-inducible kinases controls the interconversion of classically activated andregulatory macrophages. Proc Natl Acad Sci U S A. 2012 Oct 16;109(4
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