Budipine
CAS No. 57982-78-2
Budipine( —— )
Catalog No. M20845 CAS No. 57982-78-2
Budipine is a low affinity N-methyl-D-aspartate receptor antagonistis an antiparkinsonian agent.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
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| 5MG | 33 | In Stock |
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| 10MG | 55 | In Stock |
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| 25MG | 111 | In Stock |
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| 50MG | 207 | In Stock |
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| 100MG | 306 | In Stock |
|
| 200MG | 442 | In Stock |
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| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBudipine
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NoteResearch use only, not for human use.
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Brief DescriptionBudipine is a low affinity N-methyl-D-aspartate receptor antagonistis an antiparkinsonian agent.
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DescriptionBudipine is a low affinity N-methyl-D-aspartate receptor antagonistis an antiparkinsonian agent.
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In Vitro——
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In VivoBudipine (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. 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.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorN-methyl-D-aspartate
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Research Area——
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Indication——
Chemical Information
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CAS Number57982-78-2
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Formula Weight293.45
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Molecular FormulaC21H27N
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 25 mg/mL (85.19 mM)
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SMILESCC(C)(C)N1CCC(c2ccccc2)(c2ccccc2)CC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Eltze M.Multiple mechanisms of action: the pharmacological profile of budipine.J Neural Transm Suppl. 1999;56:83-105.
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