Name | GSK2646264 |
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Synonyms |
7-{2-Methoxy-6-[(4-methyl-2-pyridinyl)methoxy]phenyl}-2,3,4,5-tetrahydro-1H-3-benzazepine
1H-3-Benzazepine, 2,3,4,5-tetrahydro-7-[2-methoxy-6-[(4-methyl-2-pyridinyl)methoxy]phenyl]- |
Description | GSK2646264 (Compound 44) is a potent and selective spleen tyrosine kinase (SYK) inhibitor with a pIC50 of 7.1. GSK2646264 also inhibits other kinases with pIC50 values of 5.4, 5.4, 5.3, 5, 4.5, <4.6 and <4.3 against LCK, LRRK2, GSK3β, JAK2, VEGFR2, Aurora B and Aurora A, respectively. GSK2646264 is penetrable into the epidermis and dermis of the skin[1]. |
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Related Catalog | |
Target |
SYK:7.1 (pIC50) LCK:5.4 (pIC50) LRRK2:5.4 (pIC50) GSK3β:5.3 (pIC50) JAK2:5 (pIC50) VEGFR2:4.5 (pIC50) Aurora B:<4.6 (pIC50) Aurora A:<4.3 (pIC50) |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 517.4±50.0 °C at 760 mmHg |
Molecular Formula | C24H26N2O2 |
Molecular Weight | 374.48 |
Flash Point | 266.7±30.1 °C |
Exact Mass | 374.199432 |
LogP | 3.40 |
Vapour Pressure | 0.0±1.3 mmHg at 25°C |
Index of Refraction | 1.585 |