IP7e

Research use only, not for human use.

IP7e is a Nurr1 activator with an EC50 value of 3.9 nM.

IP7e is a Nurr1 activator with an EC50 value of 3.9 nM.(In Vivo):IP7e(10 mg/kg) attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process. IP7e preventive treatment reduces the incidence and the severity of an MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE).

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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. Animal Model:Female C57BL/6J mice (6-8 week-old) with experimental autoimmune encephalomyelitis (EAE).Dosage:10 mg/kgAdministration: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.

IP 7e | IP-7e | isoxazolo-pyridinone 7e

Others

Other Targets

ACMSD

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500164-74-9

390.439

C23H22N2O4

>98% (HPLC)

In Vitro:?DMSO : 100 mg/mL (256.13 mM)

COCCOCc1ccc(cc1)-c1cc2onc(-c3ccccc3)c2c(=O)n1C

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(-20℃)

With Ice Pack

≥ 2 years