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Usage

Uses

Used in Medical Applications:
Ethylmethylglycinexylidide serves as a local anesthetic, providing pain relief during medical procedures. It is used as an anesthetic agent for [application reason], offering a temporary loss of sensation in a specific area of the body.
Used in Cardiology:
In the field of cardiology, ethylmethylglycinexylidide is used as an antiarrhythmic agent for [application reason], helping to regulate abnormal heart rhythms and prevent complications associated with arrhythmias.
Used in Predictive Medicine:
Ethylmethylglycinexylidide is utilized as a test drug for [application reason], allowing healthcare professionals to predict individual responses to other amide local anesthetics and assess liver function, which is crucial for personalized treatment plans and medication management.
Used in Research:
ethylmethylglycinexylidide is also used in research settings for [application reason], as it provides insights into the development of new treatments for ventricular arrhythmias and atrial fibrillation, contributing to advancements in cardiovascular medicine.

InChI:InChI=1/C13H20N2O/c1-5-15(4)9-12(16)14-13-10(2)7-6-8-11(13)3/h6-8H,5,9H2,1-4H3,(H,14,16)

Relevant academic research and scientific papers

SUBSTITUTED ACETANILIDES AND BENZAMIDES FOR THE TREATMENT OF ASTHMA AND PULMONARY INFLAMMATION

Substituted acetanilide or benzamide compositions or formulations for delivery by aerosolization are described. The formulation contains an efficacious amount of acetanilide or benzamide compound able to inhibit inflammation in asthmatic lungs. Compounds of the invention are formulated in 5 ml solution of a quarter normal saline having pH between 5.0 and 7.0. The method for treatment of respiratory tract inflammation by a formulation delivered as an aerosol having mass medium average diameter predominantly between 1 to 5 μ, produced by nebulization or dry powder inhaler.

Cyclizing compounds. 3. Local anesthetic action of N (ω haloalkyl) N methylaminoaceto 2,6 xylidides

A series of N (ω chloroalkyl) N methylaminoaceto 2,6 xylidides which are able to cyclize to quaternary ammonium derivates was synthesized and examined for local anesthetic action. As reference compounds the corresponding series of N alkylamine derivates were synthesized and tested. In both series of compounds the duration of anesthesia was prolonged by increasing the size of the side chain. In the N alkylamine series an optimal effect was obtained for the N hexylamine derivate. The duration of anesthesia produced by the cyclizing compounds in the sciatic nerve test in vivo was somewhat shorter than that for the noncyclizing compounds. The observation that the N 4 chlorobutyl derivate produced a longer block than the 5 chloropentylamine in this test indicates that the quaternary compounds formed may contribute to the duration of anesthesia.