Butyl 4-aminobenzoate
CAS No. 94-25-7
Butyl 4-aminobenzoate( Butamben, Butanylcaine, Butesin, Zyljectin, Butoform, Planoform )
Catalog No. M16747 CAS No. 94-25-7
Butamben is a long-duration local anesthetic used for the treatment of chronic pain.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 500MG | 38 | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameButyl 4-aminobenzoate
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NoteResearch use only, not for human use.
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Brief DescriptionButamben is a long-duration local anesthetic used for the treatment of chronic pain.
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DescriptionButamben is a long-duration local anesthetic used for the treatment of chronic pain.(In Vitro):Butamben (500 μM) blocks 90% of the control barium current, and this level is reached within 4 min in PC12 cells.Butamben (100 μM; 2-10 min) increases the inactivation of the fast Na+ channels, but not of the slow Na+ channels.(In Vivo):Butamben (0.5-50 mM; the distal portion of the tail was immersed for 2 min) has an S-shape dose-dependent analgesic activity in the radiant heat tail-flick assay of mice.
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In VitroButamben (500 μM) blocks 90% of the control barium current, and this level is reached within 4 min in PC12 cells.Butamben (100 μM; 2-10 min) increases the inactivation of the fast Na+ channels, but not of the slow Na+ channels.
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In VivoButamben (0.5-50 mM; the distal portion of the tail was immersed for 2 min) has an S-shape dose-dependent analgesic activity in the radiant heat tail-flick assay of mice.
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SynonymsButamben, Butanylcaine, Butesin, Zyljectin, Butoform, Planoform
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PathwayMembrane Transporter/Ion Channel
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TargetSodium Channel
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RecptorSodium Channel
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number94-25-7
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Formula Weight193.24
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Molecular FormulaC11H15NO2
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESO=C(OCCCC)C1=CC=C(N)C=C1
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Chemical Namebutyl 4-aminobenzoate
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.Tzimopoulos D, et al. J Inorg Biochem. 2010 Apr;104(4):423-30.
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