Propitocaine hydrochloride
CAS No. 1786-81-8
Propitocaine hydrochloride( —— )
Catalog No. M12692 CAS No. 1786-81-8
Prilocaine hydrochloride is a local anesthetic of the amino amide type.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 50MG | 34 | In Stock |
|
| 100MG | 45 | In Stock |
|
| 200MG | 64 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NamePropitocaine hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionPrilocaine hydrochloride is a local anesthetic of the amino amide type.
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DescriptionPrilocaine hydrochloride is a local anesthetic of the amino amide type.(In Vitro):Prilocaine is more potent in inhibiting the Na,K-ATPase of plasma membranes of LM cells (transformed fibroblasts) at 37 ℃ (43.8 mM) than at 25 ℃ (28.2 mM).
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In VitroPrilocaine hydrochloride is more potent in inhibiting the Na,K-ATPase of plasma membranes of LM cells (transformed fibroblasts) at 37 ℃ (43.8 mM) than at 25 ℃ (28.2 mM).
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In Vivo——
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Synonyms——
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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 AreaOther Indications
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Indication——
Chemical Information
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CAS Number1786-81-8
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Formula Weight256.77
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Molecular FormulaC13H21ClN2O
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESCl.CCCNC(C)C(=O)NC1=CC=CC=C1C
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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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Ranolazine dihydroch...
An anti-ischemic agent that has been shown to inhibit late I(Na) and I(Kr) and to have antiarrhythmic effects in various preclinical in vitro models.
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Trapencaine
Trapencaine is a newly synthesized carbamate type local anesthetic that induces conformational changes in sodium channels on hypertrophic cell membranes.
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Huwentoxin IV
Selective NaV1.7 channel blocker. Preferentially inhibits neuronal NaV1.7, 1.2 and 1.3 (IC50 values are 26, 150 and 338 nM respectively), compared to muscle subtypes NaV1.4 and 1.5 (IC50 = >10 μM). Inhibits the channel by binding at the neurotoxin receptor site 4 in the S3-S4 linker of domain II, trapping the voltage sensor in the inward, closed configuration.
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