Name | IP7e |
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Synonyms |
6-{4-[(2-Methoxyethoxy)methyl]phenyl}-5-methyl-3-phenyl[1,2]oxazolo[4,5-c]pyridin-4(5H)-one
IP7e MFCD30182349 Isoxazolo[4,5-c]pyridin-4(5H)-one, 6-[4-[(2-methoxyethoxy)methyl]phenyl]-5-methyl-3-phenyl- |
Description | IP7e is a potent, brain-penetrant and orally active Nurr1 activator with an EC50 value of 3.9 nM[1]. |
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Related Catalog | |
Target |
EC50: 3.9 nM (Nurr1)[1] |
In Vivo | IP7e (Isoxazolo-pyridinone 7e; 10 mg/kg; oral gavage; twice a day) preventive treatment reduces the incidence and the severity of a MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE). IP7e attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process[2]. Animal Model: Female C57BL/6J mice (6-8 week-old) with experimental autoimmune encephalomyelitis (EAE)[2]. Dosage: 10 mg/kg Administration: Oral gavage; twice a day; preventive administration (before the disease onset) from 7 to 23 d.p.i. and therapeutic (after the disease onset) from 21 to 36 d.p.i. Result: Preventive administration delayed the onset and reduces the incidence and severity of EAE, and decreased neuroinflammatory and histopathological alterations in the spinal cord of treated EAE mice. On the contrary, the course of EAE was not influenced by the therapeutic administration. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 611.8±55.0 °C at 760 mmHg |
Molecular Formula | C23H22N2O4 |
Molecular Weight | 390.43 |
Flash Point | 323.8±31.5 °C |
Exact Mass | 390.157959 |
LogP | 2.61 |
Vapour Pressure | 0.0±1.8 mmHg at 25°C |
Index of Refraction | 1.593 |
Storage condition | -20°C |