PHARMACOLOGICAL STUDIES ON NOVEL BASIC AMINOALKYL ARYL ETHERS AS POTENTIAL LOCAL ANAESTHETICS
نویسندگان
چکیده مقاله:
Following our previous investigations on certain new aminoalkyl aryl ethers, which showed promising and outstanding local anaesthetic properties, the local anaesthetic activity and duration of action of a further selection of four novel derivatives of the above-mentioned series, used as hydrochloride salts, have been determined by the ill vivo rat sciatic nerve test. These are: N,N-dimethyl-2-(2,6-ditert- butylphenoxy)ethylamine N, N-dimethyl-2-(4-butoxyphenoxy) ethylamine N, N-dimethyl-2-(2,6-di-sec-butylphenoxy)ethylamine and N,N-diethyl-2-(4-secbutylphenoxy) ethylamine. The tests have been performed by a double blind, controlled trial (at the later stage) and in two stages. Bupivacaine hydrochloride has been employed as the standard and normal saline as the control. The complete loss of motor function of the injected limb of the animal is considered as a positive response, which is assessed by observing the animal gait and ability to climb up a sloping wire mesh. The test compounds have exhibited shorter duration of motor paralysis than that of the standard and comparable rates of both onset of action, and recovery time from full analgesia. They also have shown neither apparent systemic nor local side effects such as edema, swelling, induration, ulceration, necrosis, or irritation.
منابع مشابه
pharmacological studies on novel basic aminoalkyl aryl ethers as potential local anaesthetics
following our previous investigations on certain new aminoalkyl aryl ethers, which showed promising and outstanding local anaesthetic properties, the local anaesthetic activity and duration of action of a further selection of four novel derivatives of the above-mentioned series, used as hydrochloride salts, have been determined by the ill vivo rat sciatic nerve test. these are: n,n-dimethyl-2-(...
متن کاملTOXICOLOGICAL STUDIES ON CERTAIN AMINOALKYL ETHERS AS POTENTIAL LONG-ACTING LOCAL ANAESTHETICS
The acute intravenous toxicities of a selection of three potential long-acting local anaesthetics belonging to the series of2- phenoxyethyldialkylamine were determined in mice. Two of the compounds were tertiary amines and the third a quaternary ammonium derivative.The I.V. median lethal dose, (LDso) of one of the tertiary compounds, 21A [N, N- diethyl-2- (2,6- diisopropyl) ethyl amine hyd...
متن کاملtoxicological studies on certain aminoalkyl ethers as potential long-acting local anaesthetics
the acute intravenous toxicities of a selection of three potential long-acting local anaesthetics belonging to the series of2- phenoxyethyldialkylamine were determined in mice. two of the compounds were tertiary amines and the third a quaternary ammonium derivative.the i.v. median lethal dose, (ldso) of one of the tertiary compounds, 21a [n, n- diethyl-2- (2,6- diisopropyl) ethyl amine hydrochl...
متن کاملSynthesis of N-substituted aminoalkyl derivatives of some epoxyisoindoles as potential pharmacological agents.
Grogan and Rice reported a number of imides of epoxyisoindole sort. Some pharmacological testing was performed which revealed their bioactivity. Except of their work, only scattered examples of derivatives with oxygen-bridged ring have appeared in the literature; this approach has also been used by us in the synthesis of some new potential drugs. This paper reports the synthesis of a number of ...
متن کاملINVESTIGATIONS ON THE DRUG-PROTEIN IN TERAC TION OF CERTAIN NEW POTENTIAL LOCAL ANAESTHETICS
Generally, plasma proteins owe their binding capacity to the presence of aminoacid units which enter into intra- and intermolecular hydrophobic bonding with a diverse range of endo- and exogenous chemical substances. The intermolecular interactions between the hydrophobic areas of drug molecules and those of plasma proteins play an important role in drug-macromolecular complex formation and...
متن کاملRearrangements of Cycloalkenyl Aryl Ethers.
Rearrangement reactions of cycloalkenyl phenol and naphthyl ethers and the acid-catalyzed cyclization of the resulting product were investigated. Claisen rearrangement afforded 2-substituted phenol and naphthol derivatives. Combined Claisen and Cope rearrangement resulted in the formation of 4-substituted phenol and naphthol derivatives. In the case of cycloocthylphenyl ether the consecutive Cl...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ذخیره در منابع من قبلا به منابع من ذحیره شده{@ msg_add @}
عنوان ژورنال
دوره 7 شماره 3
صفحات 187- 191
تاریخ انتشار 1993-11
با دنبال کردن یک ژورنال هنگامی که شماره جدید این ژورنال منتشر می شود به شما از طریق ایمیل اطلاع داده می شود.
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023