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Acetylcholine chloride

Acetylcholine chloride [60-31-1] M 181.7, m 148-150 , 151". It is very sol in H2O (> 10%), and is very hygroscopic. If pasty, dry in a vacuum desiccator over H2SO4 undl a solid residue is obtained. Dissolve in abs EtOH, filter and add dry Et20 and the hydrochloride separates. Collect by filtration and store under very dry conditions. [J Am Chem Soc 52 310 1930.] The chloroplatinate crystallises from hot H2O in yellow needles and can be recrystd from 50% EtOH, m 242-244° [Biochem J 23 1069 7929], other m given is 256-257°. The perchlorate crystallises from EtOH as prisms m 116-117°. [J Am Pharm Assocn 36 272 1947.]... [Pg.506]

C2H3CIO 75-36-5) see Acebutolol Acetiamine Acetylcholine chloride L-Alanine Benfurodil hemisuccinate . Chlorprothixene Flumetasone Ibuprofen lotalamic acid loxitalamic acid Levodopa Methestrol dipropionate Midecamycin acetate Naproxen Nimesulide Paclitaxel Paramethasone Phensuximide Retinol Rocuronium bromide Rofecoxib Ropinirole Tazarotene Thiopropazate Tiracizine Vecuronium bromide... [Pg.2283]

C5H15NO2 123-41-1) see Acetylcholine chloride Choline chloride Choline dihydrogen citrate Choline stearate choline naphthalene-1,5-disulfonate (C20H34N2O8S2) see Aclatonium napadisilate choline tosylate... [Pg.2337]

C2H5CIO 107-07-3) see Acetylcholine chloride Carbachol Choline chloride Etofylline Homofenazine Metronidazole Oxypendyl Tofenacin Troxerutin ethylenediamine... [Pg.2379]

C3H< N 75-50-3) see Acetylcholine chloride Betaine hydrate Bethanechol chloride Carbachol Carnitine Cetrimonium bromide Choline chloride Choline hydroxide Decamethonium bromide Hexcarbacholine bromide Miltefosine Prolonium iodide... [Pg.2451]

Potential oscillation was measured in the presence of cholinergic agents (acetylcholine chloride, carbamylcholine chloride, carbamyl- d-methylcholine chloride, and acetyl-/6-methylcholine chloride) and anticholinergic agents (tetramethylammonium chloride, tetra-ethylammonium chloride, succinylcholine chloride, hexamethonium chloride, scopolamine hydrobromide, atropine sulfate, homatropine hydrochloride, and tubocurarine chloride)... [Pg.714]

FIG. 18 Chemical structures of (a) acetylcholine chloride, (b) carbamylcholine chloride, (c) carba-myl-y8-methylcholine chloride, (d) acetyl-/i-methylcholine chloride, (e) tetramethylammonium chloride, (f) tetraethylamonium chloride, (g) succinylcholine chloride, (h) hexamethonium chloride, (i) scopolamine hydrobromide, 0 atropine sulfate, (k) homatropine hydrochloride, and (1) tubocurar-ine chloride. [Pg.716]

Males were anesthetised and mental glands (N 200) were surgically removed. Secreted components were extracted into 0.8 mM acetylcholine chloride in l/2x PBS (cf Rollmann, Houck and Feldhoff 1999). Gland extracts were centrifuged for 10 min at 14,000 g and the supernatant was removed. The supernatant was filtered (0.2 pm) and loaded as aliquots onto a Sephadex Superfine G-75 gel filtration column (1.6 cm x 15.5 cm Pharmacia, Piscataway, NJ) on a Waters HPLC system (Mil-lipore, Milford, MA). The column had previously been equilibrated with one-half strength Dulbecco s phosphate buffered saline (l/2x PBS). The column was eluted... [Pg.216]

Their specimen of cholinesterase was prepared from horse serum by the method of Stedman and Stedman,1 and the method of estimation was that of Ammon.2 The enzyme solution was placed in the right-hand flask of a Barcrofb manometer, in a total volume of 3 ml. of 0-2 per cent NaHC03 solution the gas phase was 5 per cent C02 in Na. The reaction, carried out at 20°, was started by adding a solution containing 2 mg. of acetylcholine chloride. The C02 output was usually linear until about 100 fi. had been produced. [Pg.76]

Fig. 14. Inhibition of horse-serum cholinesterase by various compounds. Incubated for 15 min. at 20° before addition of 2 mg. of acetylcholine chloride. A, di-isopropyl phosphorofluoridate B, di ec.-butyl phosphorofluoridate C, eserine D, diphenyl phosphorofluoridate E, dithioethyl phosphorofluoridate F, tetramethylphosphorodiamidic fluoride O, diethyl ALmethylphosphor-amidate. Fig. 14. Inhibition of horse-serum cholinesterase by various compounds. Incubated for 15 min. at 20° before addition of 2 mg. of acetylcholine chloride. A, di-isopropyl phosphorofluoridate B, di ec.-butyl phosphorofluoridate C, eserine D, diphenyl phosphorofluoridate E, dithioethyl phosphorofluoridate F, tetramethylphosphorodiamidic fluoride O, diethyl ALmethylphosphor-amidate.
Molitor H A comparative study of the effects of five choline compounds used in therapeutics Acetylcholine chloride, acetyl-beta-methylcholine chloride, carbaminoyl choline, ethyl ether beta-methylcholine chloride, carbaminoyl betamethylcholine chloride. J Pharmacol Exp Ther 1936 58 337. [Pg.151]

Ophthalmic preparations containing acetylcholine chloride and carbacol were found infective in patients receiving topical NSAIDs. [Pg.341]

See other pages where Acetylcholine chloride is mentioned: [Pg.549]    [Pg.20]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.2280]    [Pg.2328]    [Pg.2337]    [Pg.2380]    [Pg.419]    [Pg.78]    [Pg.420]    [Pg.1115]    [Pg.2085]    [Pg.2085]    [Pg.2086]    [Pg.270]    [Pg.132]    [Pg.238]    [Pg.1099]    [Pg.84]    [Pg.445]    [Pg.131]    [Pg.338]    [Pg.20]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.21]    [Pg.2280]    [Pg.2283]    [Pg.2328]    [Pg.2337]   
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