1042673-20-0

JH-I-25 Chemical Structure
1042673-20-0

Chemical Structure

JH-I-25

  • CAS No.: 1042673-20-0
  • Formula:C20H21N5O3
  • Molecular Weight:379.42

IUPAC Name: N-(2-methoxy-4-morpholinophenyl)-6-(1H-pyrazol-3-yl)picolinamide

InChIKey: RAFFLDOJXQAJPF-UHFFFAOYSA-N

SMILES: O=C(NC1=CC=C(C=C1OC)N2CCOCC2)C3=NC(=CC=C3)C4=NNC=C4

Biological Activity: JH-I-25 is an orally active IRAK1 and IRAK4 inhibitor. JH-I-25 inhibits LPS-induced IRAK4 phosphorylation, IRAK1 degradation, MAPK activation, and the expression of proinflammatory cytokines TNF-α and IL-6 in lung tissues. JH-I-25 improves the survival rate of LPS-induced septic mice and serves as an IRAK4 recruiter in the design of proteolysis-targeting chimeric molecules. JH-I-25 can be used in research related to diffuse large B-cell lymphoma, Waldenström's macroglobulinemia, septic shock, rheumatoid arthritis, atherosclerosis, Alzheimer's disease, acute lung injury, sepsis, and psoriasis[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-138834
JH-I-25 JH-I-25 is an orally active IRAK1 and IRAK4 inhibitor. JH-I-25 inhibits LPS-induced IRAK4 phosphorylation, IRAK1 degradation, MAPK activation, and the expression of proinflammatory cytokines TNF-α and IL-6 in lung tissues. JH-I-25 improves the survival rate of LPS-induced septic mice and serves as an IRAK4 recruiter in the design of proteolysis-targeting chimeric molecules. JH-I-25 can be used in research related to diffuse large B-cell lymphoma, Waldenström's macroglobulinemia, septic shock, rheumatoid arthritis, atherosclerosis, Alzheimer's disease, acute lung injury, sepsis, and psoriasis.
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