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 |
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| 200MG | 442 | In Stock |
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| 500MG | Get Quote | In Stock |
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| 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
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Dieugenol
Dieugenol is a neolignan that has been found in N. leucantha and has antioxidative and antiprotozoal activities. It inhibits the formation of thiobarbituric acid reactive substances (TBARS) and scavenges superoxide anions, but not hydroxyl radicals, in cell-free assays. It has anti-trypanosomal activity against T. cruzi amastigotes and trypomastigotes (IC50s=15.1 and 11.5 μM, respectively) but is cytotoxic to NCTC L-929 fibroblasts with a 50% cytotoxic concentration (CC50) value of 58.2 μM.2 Dieugenol (15 μM) disrupts the integrity of the T. cruzi trypomastigote plasma membrane but does not induce the production of reactive oxygen species (ROS) in trypomastigotes or LPS-stimulated and unstimulated isolated mouse peritoneal macrophages.
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