Name | 4-[4-(6-methoxynaphthalen-2-yl)-2-(4-methylsulfinylphenyl)-1H-imidazol-5-yl]pyridine |
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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]. |
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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 |
Density | 1.4±0.1 g/cm3 |
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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 |
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