Budipine is an anti-parkinson agent. Budipine also is a substrate of P-glycoprotein (P-gp), is mediated the uptake into the brain by P-gp. Budipine also is N-methyl-d-aspartate (NMDA) antagonist, and has indirect dopaminergic effects through an improved dopamine release, the inhibition of monoamine oxidase type B (MAO-B). Budipine can be used for the research of CNS disorders include Parkinson disease In Vivo Budipine (s.c., 30 μg/24 h, 11 days) is a substrate of P-glycoprotein (P-gp) and is actively transported out of the brain through the blood–brain barrier back into the blood plasma . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Male abcblab(-/-) mice Male abcblab(-/-) mice (n=8, weight 29.0 g) and FVB/N wild-type mice (n =8, weight 28.0 g) Dosage: 30 μg (Budipine is dissolved in 0.9% sodium chloride and 0.5% ethanol) Administration: subcutaneous injections, continuously delivered 30 μg over 24 h, 11 days Result: Increased the cerebrum concentration for 3.1 times high in knock-out mice after an 11-day continuous administration. Showed no significant differences in plasma, spleen, kidney and liver. Form:Solid IC50& Target:NMDA Receptor
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Budipine
CAS number:57982-78-2 molecular formula:C21H27N
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| Chinese alias | 布地平 | ||
| English alias | BRN 5959608 | AKOS015949499 | BUDIPINE [MART.] | Budipin | EINECS 261-062-4 | DTXSID20206709 | Budipina [INN-Spanish] | 1-(t-Butyl)-4,4-diphenylpiperidine | Budipinum | DB13502 | J-505146 | SCHEMBL120041 | 1-tert-Butyl-4,4-diphenylpiperidine | 1-tert-Buty | ||
| CAS number | 57982-78-2 | molecular formula | C21H27N |
| molecular weight | 293.4 g/mol | Exact mass | ≥99% |
| PSA | 3.200 Ų | logp | 5.200 |
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