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948557-43-5

948557-43-5 structure
948557-43-5 structure
  • Name: Tie2 kinase inhibitor
  • Chemical Name: 4-[4-(6-methoxynaphthalen-2-yl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine
  • CAS Number: 948557-43-5
  • Molecular Formula: C26H21N3O2S
  • Molecular Weight: 439.529
  • Catalog: Biochemical Inhibitor Protein tyrosine kinase
  • Create Date: 2018-11-29 06:58:51
  • Modify Date: 2024-01-14 00:53:04
  • Tie2 kinase inhibitor 1 (compound 5) is a potent, selective Tie2 kinase inhibitor with an IC50 of 250 nM[1]. Tie2 kinase inhibitor 1 has anti-cancer activity[2].

Name 4-[4-(6-methoxynaphthalen-2-yl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine
Synonyms S1577_Selleck
X7496
4-{4-(6-Methoxy-2-naphthyl)-2-[4-(methylsulfinyl)phenyl]-1H-imidazol-5-yl}pyridine
Tie2 kinase inhibitor-Supplied by Selleck Chemicals
4-{4-(6-methoxynaphthalen-2-yl)-2-[4-(methylsulfinyl)phenyl]-1H-imidazol-5-yl}pyridine
Pyridine, 4-[4-(6-methoxy-2-naphthalenyl)-2-[4-(methylsulfinyl)phenyl]-1H-imidazol-5-yl]-
Tie2 kinase inhibitor
Description Tie2 kinase inhibitor 1 (compound 5) is a potent, selective Tie2 kinase inhibitor with an IC50 of 250 nM[1]. Tie2 kinase inhibitor 1 has anti-cancer activity[2].
Related Catalog
Target

IC50: 250 nM (Tie2)[1]

In Vitro Tie2 kinase inhibitor 1 (compound 5) has an IC50 of 50 μM for p38 and has moderate to excellent cellular activities (cell IC50=232 nM)[1]. Tie2 kinase inhibitor 1 inhibits tunica internal endothelial cell kinase 2 (Tie2)[2].
In Vivo Tie2 kinase inhibitor 1 (intraperitoneally; 50 mg/kg; twice a week for 6 weeks) results in statistically significant reductions in tumor volume by day 15. Tie2 kinase inhibitor 1 results in a 61% reduction in tumor volume by day 20, and reduces tumor volume by 45% by 6 weeks[1]. Animal Model: Athymic nude mice (6- to 8-week-old females)[1] Dosage: 50 mg/kg Administration: Intraperitoneally; twice a week for 6 weeks Result: Resulted in statistically significant reductions in tumor volume.
References

[1]. Semones M, et al. Pyridinylimidazole inhibitors of Tie2 kinase. Bioorg Med Chem Lett. 2007 Sep 1;17(17):4756-60. Epub 2007 Jun 27.

[2]. Hasenstein JR, et al. Efficacy of Tie2 receptor antagonism in angiosarcoma. Neoplasia. 2012 Feb;14(2):131-40.

Density 1.4±0.1 g/cm3
Boiling Point 699.8±55.0 °C at 760 mmHg
Molecular Formula C26H21N3O2S
Molecular Weight 439.529
Flash Point 377.0±31.5 °C
Exact Mass 439.135437
PSA 87.08000
LogP 5.31
Vapour Pressure 0.0±2.1 mmHg at 25°C
Index of Refraction 1.746
Storage condition -20℃
Hazard Codes N