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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References