Valpramide
CAS No. 2430-27-5
Valpramide( Valpromide | Depamide )
Catalog No. M13702 CAS No. 2430-27-5
Valpromide is a carboxamide derivative of valproic acid used in the treatment of epilepsy and some affective disorders.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 29 | In Stock |
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| 50MG | 28 | In Stock |
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| 100MG | 41 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | 91 | In Stock |
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| 1G | 138 | In Stock |
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Biological Information
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Product NameValpramide
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NoteResearch use only, not for human use.
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Brief DescriptionValpromide is a carboxamide derivative of valproic acid used in the treatment of epilepsy and some affective disorders.
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DescriptionValpromide is a carboxamide derivative of valproic acid used in the treatment of epilepsy and some affective disorders.
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In Vitro——
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In Vivo——
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SynonymsValpromide | Depamide
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PathwayOthers
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TargetOther Targets
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Recptor2-epoxide hydrolase| Limonene-1
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Research Area——
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Indication——
Chemical Information
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CAS Number2430-27-5
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Formula Weight143.23
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Molecular FormulaC8H17NO
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESCCCC(CCC)C(N)=O
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Chemical Name2-propylpentanamide
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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24-Norursodeoxycholi...
24-norursodeoxycholic acid is a side chain-shortened C23 homolog of UDCA.It has shown potent anti-inflammatory, anti-cholestatic, and anti-fibrotic properties.It is a Ursodeoxycholic Acid derivative. It is superior to Ursodeoxycholic acid in the treatment of sclerosing cholangitis in Mdr2 (Abcb4) knockout mice24-norUrsodeoxycholic acid markedly improved liver tests and liver histology and significantly reduced hydroxyproline content and the number of infiltrating neutrophils and proliferating hepatocytes and cholangiocytes.?
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Dcimc chloride
3-(2, 6-Dichlorophenyl)-5-methylisoxazole-4-carbonyl chloride has antibiotics activity.
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2-Hydroxy atorvastat...
2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt which is a potent HMG-CoA reductase inhibitor (IC50 = 8 nM).
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