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1493764-08-1

1493764-08-1 structure
1493764-08-1 structure
  • Name: UNC 2881
  • Chemical Name: 5-​Pyrimidinecarboxamid​e, 2-​(butylamino)​-​4-​[(trans-​4-​hydroxycyclohexyl)​amino]​-​N-​[[4-​(1H-​imidazol-​1-​yl)​phenyl]​methyl]​-
  • CAS Number: 1493764-08-1
  • Molecular Formula: C25H33N7O2
  • Molecular Weight: 463.575
  • Catalog: Biochemical Inhibitor Protein tyrosine kinase
  • Create Date: 2018-12-03 11:30:44
  • Modify Date: 2025-08-25 00:36:18
  • UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer kinase phosphorylation with an IC50 value of 22 nM. IC50 value: 22 nM [1]Target: Mer kinase inhibitorTreatment with UNC2281 is also sufficient to block EGF-mediated stimulation of a chimeric receptor containing the intracellular domain of Mer fused to the extracellular domain of EGFR. In addition, UNC2881 potently inhibits collagen-induced platelet aggregation, suggesting that this class of inhibitors may have utility for prevention and/or treatment of pathologic thrombosis.

Name 5-​Pyrimidinecarboxamid​e, 2-​(butylamino)​-​4-​[(trans-​4-​hydroxycyclohexyl)​amino]​-​N-​[[4-​(1H-​imidazol-​1-​yl)​phenyl]​methyl]​-
Synonyms 5-Pyrimidinecarboxamide, 2-(butylamino)-4-[(trans-4-hydroxycyclohexyl)amino]-N-[[4-(1H-imidazol-1-yl)phenyl]methyl]-
2-(Butylamino)-4-[(trans-4-hydroxycyclohexyl)amino]-N-[4-(1H-imidazol-1-yl)benzyl]-5-pyrimidinecarboxamide
UNC2881
Description UNC2881 is a potent and specific Mer kinase inhibitor; inhibits steady-state Mer kinase phosphorylation with an IC50 value of 22 nM. IC50 value: 22 nM [1]Target: Mer kinase inhibitorTreatment with UNC2281 is also sufficient to block EGF-mediated stimulation of a chimeric receptor containing the intracellular domain of Mer fused to the extracellular domain of EGFR. In addition, UNC2881 potently inhibits collagen-induced platelet aggregation, suggesting that this class of inhibitors may have utility for prevention and/or treatment of pathologic thrombosis.
Related Catalog
References

[1]. Zhang W, et al. Discovery of Mer specific tyrosine kinase inhibitors for the treatment and prevention of thrombosis. J Med Chem. 2013 Dec 12;56(23):9693-700.

Density 1.3±0.1 g/cm3
Molecular Formula C25H33N7O2
Molecular Weight 463.575
Exact Mass 463.269562
PSA 116.99000
LogP 3.03
Index of Refraction 1.666
Storage condition -20℃
Water Solubility Insuluble (1.7E-3 g/L) (25 ºC)
Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H302
Precautionary Statements P301 + P312 + P330
RIDADR NONH for all modes of transport
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