2374699-35-9

JH-XIII-05-01 Chemical Structure
2374699-35-9

Chemical Structure

JH-XIII-05-01

  • CAS No.: 2374699-35-9
  • Formula:C46H51N11O10
  • Molecular Weight:917.96

IUPAC Name: N-(3-(1-(1-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino)-3,6,9,12-tetraoxapentadecan-15-oyl)piperidin-4-yl)-1-(pyridin-2-yl)-1H-pyrazol-5-yl)-6-(1H-pyrazol-5-yl)picolinamide

InChIKey: OYHCKWFUEKWODK-UHFFFAOYSA-N

SMILES: O=C(C1=NC(C2=CC=NN2)=CC=C1)NC3=CC(C4CCN(C(CCOCCOCCOCCOCCNC5=CC=CC(C(N6C7CCC(NC7=O)=O)=O)=C5C6=O)=O)CC4)=NN3C8=CC=CC=N8

Biological Activity: JH-XIII-05-01 is a cereblon-recruiting PROTAC degrader targeting IRAK1 and IRAK4, with DC50 values of 0.065 μM and 3.63 μM, respectively (TMD8 cells). JH-XIII-05-01 reduces cancer cell viability, induces apoptosis in primary MYD88-mutant WM cells and MYD88-mutant/wild-type lymphoma cells, and selectively degrades additional cereblon neosubstrates and kinases IKZF1, IKZF3, CSNK1A1, CSNK1D, CSNK1E, and PAK4. JH-XIII-05-01 can be used for research on Waldenström macroglobulinemia, diffuse large B-cell lymphoma, and B-cell lymphoma[1][2].

Cat. No. Product Name Purity Description Pricing
HY-133616
JH-XIII-05-01 JH-XIII-05-01 is a cereblon-recruiting PROTAC degrader targeting IRAK1 and IRAK4, with DC50 values of 0.065 μM and 3.63 μM, respectively (TMD8 cells). JH-XIII-05-01 reduces cancer cell viability, induces apoptosis in primary MYD88-mutant WM cells and MYD88-mutant/wild-type lymphoma cells, and selectively degrades additional cereblon neosubstrates and kinases IKZF1, IKZF3, CSNK1A1, CSNK1D, CSNK1E, and PAK4. JH-XIII-05-01 can be used for research on Waldenström macroglobulinemia, diffuse large B-cell lymphoma, and B-cell lymphoma.
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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