Pharmaceutical intermediates136-47-0 Tetracaine hydrochloride
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- Purity: 99%
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Keywords
136-47-0 Danger Pharmaceutical intermediates
Quick Details
- Appearance: White crystal
- Application:Tetracaine hydrochloride is an effective local anesthetic and an allosteric inhibitor of channel functionIt is mainly used in ophthalmology and antipruritic, and has been used in spinal anesthesia
- PackAge:sliver bags /boxes 1kg /bags 25kg/big boxes
- ProductionCapacity:20|Metric Ton|Day
- Storage:The refrigerator
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API Tetracaine HCl Powder Dosage Usage Effect and Benefit
Tetracaine hydrochloride is an effective local anesthetic and an allosteric inhibitor of channel function.Objective: calcium channel tetracaine hydrochloride is a calcium channel protein inhibitor that prevents the release of calcium-sensitive Ca2 + in the sarcoplasmic reticulum.Tetracaine is a strong local anesthetic of ester group.It is mainly used in ophthalmology and antipruritic, and has been used in spinal anesthesia.Tetracaine is used to change the function of the ryanodine receptor, which controls the release of calcium from intracellular stores.Tetracaine is a channel - function allosteric blocker.At low concentrations, tetracaine leads to initial inhibition of spontaneous calcium release events, whereas at high concentrations, tetracaine blockers are completely released [1, 2].
Details:
Tetracaine hydrochloride is an effective local anesthetic and an allosteric inhibitor of channel function.Objective: calcium channel tetracaine hydrochloride is a calcium channel protein inhibitor that prevents the release of calcium-sensitive Ca2 + in the sarcoplasmic reticulum.Tetracaine is a strong local anesthetic of ester group.It is mainly used in ophthalmology and antipruritic, and has been used in spinal anesthesia.Tetracaine is used to change the function of the ryanodine receptor, which controls the release of calcium from intracellular stores.Tetracaine is a channel - function allosteric blocker.At low concentrations, tetracaine leads to initial inhibition of spontaneous calcium release events, whereas at high concentrations, tetracaine blockers are completely released [1, 2].
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