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Carbachol chloride

CAPTAN SC , captan, 35 Carbachol chloride, 35 Carbagas, 156, 203 Carbamic acid ethyl ester, 35 Carbaryl, 35... [Pg.325]

Carbamylcholine chloride [51 -83-2] is also called carbachol (47). Its principal use is as a parasympathornimetic in veterinary practice for large animals. [Pg.102]

Choline theophyllinate Choline chloride Carbachol Choline salicylate Choline dihydrogen citrate Ferrocholinate Chromic acid... [Pg.1624]

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]

Salim (1992d) has performed several studies using reser-pine to produce a chronic model of peptic ulceration in rats. Administration of allopurinol, DMSO, cysteine or methionine-S-methylsulphonium chloride protected against injury. In addition allopurinol and DMSO were found to stimulate healing in this model. In an acute model of duodenal ulceration induced by pentagastrin and carbachol allopurinol, DMSO, cysteine or methionine-S-methylsulphonium chloride all protected against injury. [Pg.146]

Carbachol Carbachol, 2-carbamoyloxy-iV,iV,iV-trimethylethyl ammonium chloride (13.1.7), is made by reacting 2-chloroethanol with phosgene, which forms 2-chloroethyl chloroformate (13.1.5). Upon reaction with ammonia, it turns into the corresponding amide (13.1.6), which is further reacted with an equimolar quantity of trimethylamine, giving carbachol (13.1.7) [9-13],... [Pg.182]

Betanechol Betanechol, 2-carbamoyloxy-l-(A,A,iV-trimethyl)propyl ammonium chloride (13.1.8), is made by either the subsequent reaction of l-(iV,A,A-trimethylammonium) propan-2-ol with phosgene, followed by ammonia, or by a completely analogous synthesis of carbachol by the reaction of l-chloro-2-propanol with phosgene followed by consequent reactions with ammonia, and then with trimethylamine, giving betanechol (13.1.8) [14,15],... [Pg.182]

Alcuronium Chloride Benserazide Bethanidine Bretylium Tosylate Carbachol Debrisoquine Dibromopropamidine Dihydrostreptomycin Guanethidine Guanoxan Hexylcaine Homatropine Hydroxystilbamidine Hyoscine Kanamycin Mepenzolate Bromide Metformin Obidoxime Chloride Pancuronium Bromide Pentamidine Pentapiperide Propamidine Pyrithidium Bromide Suxamethonium Chloride Suxethonium Bromide Thiamine... [Pg.1094]

Carbachol. Choline chloride carbamate is nonspecific in its action on muscarinic receptor. subtypes. The pharmaco-... [Pg.559]

Bethanechol Chloride, USP. Bethanechol. jS-mcthyl-choline chloride carbamate. (2-hydroxypropyl)trimethylam-monium chloride carbamate, carbamylmelhylcholinc chloride (Urecholinc), is nonspecific in its action on muscarinic receptor. subtypes but appears to be more effective at eliciting pharmacological action of M> receptors. It has pharmacological properties similar to those of methacholinc. Both are esters of nicthylcholine and have feeble nicotinic activity. Bethanechol is inactivated more slowly by AChE in vivo than is mcthacholine. It is a carbamyl ester and is expected to have stability in aqueous solutions similar to that of carbachol. [Pg.560]

A few typical examples of medicinal compormds bleonging to this category are discussed below acetylcholine chloride bethanechol chloride carbachol methacholine chloride pilocarpine nitrate, etc. [Pg.399]

Carbachol may be prepared by reacting choline chloride with phosgene in chloroform solution followed by treatment of the product with ammonium hydroxide. [Pg.401]

See other pages where Carbachol chloride is mentioned: [Pg.255]    [Pg.35]    [Pg.49]    [Pg.132]    [Pg.35]    [Pg.131]    [Pg.255]    [Pg.49]    [Pg.49]    [Pg.560]    [Pg.545]    [Pg.35]    [Pg.134]    [Pg.312]    [Pg.255]    [Pg.35]    [Pg.49]    [Pg.132]    [Pg.35]    [Pg.131]    [Pg.255]    [Pg.49]    [Pg.49]    [Pg.560]    [Pg.545]    [Pg.35]    [Pg.134]    [Pg.312]    [Pg.79]    [Pg.2434]    [Pg.413]    [Pg.622]    [Pg.623]    [Pg.624]    [Pg.537]    [Pg.374]    [Pg.2434]    [Pg.1151]    [Pg.385]    [Pg.560]    [Pg.33]    [Pg.75]    [Pg.198]    [Pg.40]    [Pg.130]    [Pg.162]   
See also in sourсe #XX -- [ Pg.35 ]

See also in sourсe #XX -- [ Pg.373 ]

See also in sourсe #XX -- [ Pg.35 ]



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Choline chloride Carbachol

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