LY2228820

For research use only. Not for therapeutic Use.

  • CAT Number: I005171
  • CAS Number: 862507-23-1
  • Molecular Formula: C₂₆H₃₇FN₆O₆S₂
  • Molecular Weight: 612.74
  • Purity: ≥95%
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LY2228820(Cat No.:I005171), also known as Ralimetinib, is a selective inhibitor of p38 MAPK (mitogen-activated protein kinase). It plays a crucial role in modulating cellular responses to stress and inflammation, making it a valuable compound in cancer and inflammatory disease research. By blocking p38 MAPK activity, LY2228820 inhibits the production of pro-inflammatory cytokines and limits cancer cell proliferation. This compound has been investigated in clinical trials for its potential to enhance the efficacy of chemotherapy and other targeted therapies, particularly in solid tumors like ovarian and breast cancer.


Catalog Number I005171
CAS Number 862507-23-1
Synonyms

5-[2-tert-butyl-4-(4-fluorophenyl)-1H-imidazol-5-yl]-3-(2,2-dimethylpropyl)imidazo[4,5-b]pyridin-2-amine;methanesulfonic acid

Molecular Formula C₂₆H₃₇FN₆O₆S₂
Purity ≥95%
Target Autophagy
Solubility DMSO:38mg/mL
Storage 3 years -20C powder
IC50 7/3 nM(p38α/p38β MAPK)
IUPAC Name 5-[2-tert-butyl-4-(4-fluorophenyl)-1H-imidazol-5-yl]-3-(2,2-dimethylpropyl)imidazo[4,5-b]pyridin-2-amine;methanesulfonic acid
InChI InChI=1S/C24H29FN6.2CH4O3S/c1-23(2,3)13-31-20-17(28-22(31)26)12-11-16(27-20)19-18(14-7-9-15(25)10-8-14)29-21(30-19)24(4,5)6;2*1-5(2,3)4/h7-12H,13H2,1-6H3,(H2,26,28)(H,29,30);2*1H3,(H,2,3,4)
InChIKey NARMJPIBAXVUIE-UHFFFAOYSA-N
SMILES CC(C)(C)CN1C2=C(C=CC(=N2)C3=C(N=C(N3)C(C)(C)C)C4=CC=C(C=C4)F)N=C1N.CS(=O)(=O)O.CS(=O)(=O)O
Reference

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<br>[1]. Mader M, et al. Imidazolyl benzimidazoles and imidazo[4,5-b]pyridines as potent p38alpha MAP kinase inhibitors with excellent in vivo antiinflammatory properties. Bioorg Med Chem Lett, 2008, 18(1), 179-183.
<br>[2]. Ishitsuka K, et al. p38 mitogen-activated protein kinase inhibitor LY2228820 enhances bortezomib-induced cytotoxicity and inhibits osteoclastogenesis in multiple myeloma; therapeutic implications. Br J Haematol, 2008, 141(5), 598-606.
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