2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- manufacturers
- JH-X-119-01
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- $60.00
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2026-05-11
- CAS:2227368-54-7
- Purity: 98.42%
- Supply Ability: 10g
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| | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- Basic information |
| Product Name: | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- | | Synonyms: | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)-;JH-X-119-01;N-(4-(3-Acrylamidobenzamido)phenyl)-6-(1H-pyrazol-3-yl)picolinamide;inhibit,MYD88,IRAK,IL-1R associated kinase,Waldenstr?m,Inhibitor,IRAK1,Interleukin-1 receptor associated kinase,JHX11901,Diffused Large B-cell Lymphoma,JH X 119 01,macroglobulinemia;JH-X-119-01, 10 mM in DMSO;JH-X-119-01 ,S9780 | | CAS: | 2227368-54-7 | | MF: | C25H20N6O3 | | MW: | 452.46 | | EINECS: | | | Product Categories: | | | Mol File: | 2227368-54-7.mol | ![2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- Structure](CAS/20200611/GIF/2227368-54-7.gif) |
| | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- Chemical Properties |
| Boiling point | 654.0±55.0 °C(Predicted) | | density | 1.405±0.06 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | DMSO : 250 mg/mL (552.54 mM; Need ultrasonic) | | pka | 10.98±0.70(Predicted) | | form | Solid | | color | Light yellow to brown |
| | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- Usage And Synthesis |
| Uses | JH-X-119-01 is a potent and selective interleukin-1 receptor-associated kinases 1 (IRAK1) inhibitor. JH-X-119-01 ameliorates LPS-induced sepsis in mice[1]. JH-X-119-01 inhibits IRAK1 biochemically with an apparent IC50 of 9 nM while exhibiting no inhibition of IRAK4 at concentrations up to 10 μM[2]. | | in vivo | JH-X-119-01 improves survival and decreases immunopathies of LPS-challenged mice. JH-X-119-01 increases survival of mice at the dose of 5 mg/kg body weight. Survival is further improved when the dose is increased to 10 mg/kg[1]. | Animal Model: | C57BL/6 (20-22 g, male) mice[1] | | Dosage: | 5 mg/kg and 10 mg/kg | | Administration: | Intraperitoneally injected; 5 days | | Result: | Protected mice from LPS (20 mg/kg)-induced sepsis. Survival at day 5 was 13.3% in control group where septic mice were treated by vehicle, while the values were 37.5% and 56.3% for 5 mg/kg and 10 mg/kg. |
| | IC 50 | IRAK-1: 9 nM (IC50) | | References | [1] Bin Pan, et al. Selective inhibition of interleukin-1 receptor-associated kinase 1 ameliorates lipopolysaccharide-induced sepsis in mice. Int Immunopharmacol. 2020 Aug;85:106597. DOI:10.1016/j.intimp.2020.106597 [2] John M Hatcher, et al. Discovery of a Selective, Covalent IRAK1 Inhibitor with Antiproliferative Activity in MYD88 Mutated B-Cell Lymphoma. ACS Med Chem Lett. 2020 Oct 9;11(11):2238-2243. DOI:10.1021/acsmedchemlett.0c00378 |
| | 2-Pyridinecarboxamide, N-[4-[[3-[(1-oxo-2-propen-1-yl)amino]benzoyl]amino]phenyl]-6-(1H-pyrazol-3-yl)- Preparation Products And Raw materials |
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