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AVL-292

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AVL-292 Basic information

Product Name:
AVL-292
Synonyms:
  • AVL-292
  • LMK-435
  • N-[3-[[5-Fluoro-2-[[4-(2-methoxyethoxy)phenyl]amino]-4-pyrimidinyl]amino]phenyl]-2-propenamide
  • 2-Propenamide, N-[3-[[5-fluoro-2-[[4-(2-methoxyethoxy)phenyl]amino]-4-pyrimidinyl]amino]phenyl]-
  • CC-292 (AVL-292)
  • CC-292,LMK-435
  • N-[3-[[5-Fluoro-2-[[4-(2-methoxyethoxy)phenyl]amino]-4-pyrimidinyl]amino]phenyl]-2-propenamide AVL292
  • CC-292
CAS:
1202757-89-8
MF:
C22H22FN5O3
MW:
423.44
Product Categories:
  • Inhibitors
Mol File:
1202757-89-8.mol
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AVL-292 Chemical Properties

Density 
1.322±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
≥21.15 mg/mL in DMSO; insoluble in H2O; ≥4.9 mg/mL in EtOH with gentle warming and ultrasonic
form 
solid
pka
13.22±0.70(Predicted)
CAS DataBase Reference
1202757-89-8
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AVL-292 Usage And Synthesis

Uses

Bruton’s tyrosine kinase (BTK) is a non-receptor tyrosine kinase involved in signal transduction pathways regulating the proliferation, activation, and differentiation of B cells. AVL-292 is an orally available, selective, and irreversible inhibitor of BTK (IC50 = 0.5 nM in vitro in B cell lymphoma cell lines) that targets and covalently binds to BTK at cysteine-481, thereby preventing its activity. AVL-292 has been shown to inhibit osteoclast function and to reduce osteoclast-stimulated proliferation of multiple myeloma cells in animal models of rheumatoid arthritis and multiple sclerosis, both of which are diseases where B cells play an important role. In clinical trials, AVL-292 has demonstrated therapeutic significance in the treatment of both B cell-related cancers (e.g., non-Hodgkin’s lymphoma and B cell chronic lymphocytic leukemia) and autoimmune diseases (e.g., rheumatoid arthritis).[Cayman Chemical]

target

Btk

AVL-292Supplier

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AVL-292(1202757-89-8)Related Product Information