Chemical Structure : JNJ-1013
CAS No.: 2597343-08-1
Catalog No.: PC-27068Not For Human Use, Lab Use Only.
JNJ-1013 is a highly potent, selective interleukin-1 receptor-associated kinase 1 (IRAK1) PROTAC degrader with DC50 of 3 nM in HBL-1 cells, Dmax=96%.
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|---|---|---|---|
| 5 mg | $188 | In stock | |
| 10 mg | $298 | In stock | |
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| 100 mg | Get quote |
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JNJ-1013 is a highly potent, selective interleukin-1 receptor-associated kinase 1 (IRAK1) PROTAC degrader with DC50 of 3 nM in HBL-1 cells, Dmax=96%.
JNJ-1013inhibits cell proliferation of HBL-1 cells with IC50 of 0.06 uM.
JNJ-1013 induces apoptosis and increases the expression of cleavaged PARP.
JNJ-1013 potently inhibited IRAK1 downstream signaling pathways and demonstrated strong anti-proliferative effects in ABC DLBCL cells with MyD88 mutation.
| M.Wt | 878.06 | |
| Formula | C46H55N9O7S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
N-(4-(4-(2-(((S)-1-((2S,4R)-4-Hydroxy-2-(((S)-1-(4-(4-methylthiazol-5-yl)phenyl)ethyl)carbamoyl)pyrrolidin-1-yl)-3,3-dimethyl-1-oxobutan-2-yl)amino)-2-oxoethoxy)piperidin-1-yl)-2-methoxyphenyl)-6-(1H-pyrazol-5-yl)picolinamide |
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1. Liqiang Fu, et al. J Med Chem. 2021 Aug 12;64(15):10878-10889.

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