Atropine methobromide

YELLOW Amprolium, atropine methobromide, hyoscine butylbromide, hyoscine methobromide, ketoprofen, pipazethate, tetrahy-drozoline, tetramisole, trimetaphan... 

Aletamine, alverine, ampicillin, atropine methobromide, atropine methonitrate, baclofen, benactyzine brown), bethanidine (-> brown), broxyquinoline, butanilicaine, chloroquine (100°), clidinium (-> brown), cyclandelate, cyclizine, dazomet, decoquinate (slow), diethylthiambutene (100°), dimefline, diuron, doxapram, dyclonine (100°), fenclofenac (100°— brown), fenitrothion, fenpipramide, glibenclamide (100°,... 

Indoramin Hydrochloride Atropine Methobromide Fenoterol Hydrobromide Caramiphen Edisylate Ethynodiol Diacetate Megestrol Acetate Cholecalciferol Bamifylline... 

Atropine methobromide, 365 Atropine methonitrate, 365 Atropine methylbromide, 365 Atropine oxide, 365 Atropine oxide hydrochloride, 365 Atropine sulpha.te, 364 Atropinol, 363 Atropisol, 364 Atropt, 364... 

Phenylglycollyltropeine Mandelyltropeine, homatropine), CigHjiOjN. This is largely used as a substitute for atropine. It crystallises in prisms, m.p. 95-5-98-5°. The hydrobromide, the salt usually employed in medicine, is a crystalline powder, m.p. 217-8° (dec.) the hydrochloride, m.p. 224-5°, and the salicylate are also used. All tl ee are freely soluble in water. The methobromide has m.p. 192-6°. The aurichloride, B. HAUCI4, forms prisms and is sparingly soluble in water. Homatropine, unlike atropine, does not give the Vitali colour reaction (p. 70). Its mydriatic effect is more rapid and transient than that of atropine. 

Of the proximate derivatives of atropine, the methobromide and the methonitrate are in use for much the same purposes as atropine, but the methonitrate has received special attention for the treatment of pyloric stenosis. opoAtropine has been found by Mancini to retain the same type of action as atropine but to be less potent in peripheral and more active in central nervous action. ... 

Replacement of tropic acid in atropine with the homologous mandelic acid (a-hydrox-yphenylacetic, Table 8-8) produces homatropine, whose quatemized methobromide is still in use, as is the methobromide of scopolamine. 

Synonyms 3-(3-Hydroxy-l-oxo-2-phenylpropoxy)-8-methyl-8-(l-methylethyl)-8-azoniabicyclo[3.2.1]octane bromide 8-isopropylnoratropine methobromide atropine isopropylbromide... 

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