1950
DOI: 10.1136/bmj.1.4665.1296
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Dimethyl Ether of D-Tubocurarine Iodide as a Curarizing Agent in Anaesthesia for Thoracic Surgery

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Cited by 11 publications
(2 citation statements)
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“…It may be seen from table I that dimethyltubocurarine 9.17 mg was needed per m 2 during 90 min, while tubocurarine 18.3 mg was needed under similar conditions (Stovner, Theodorsen and Bjelke, 1971a). This makes dimethyltubocurarine twice as potent as tubocurarine, a finding which is in good agreement with that of Wilson, Gordon and Raffan (1950). It is interesting that methyl substitution in tubocurarine has resulted in a compound with higher blocking activity, while in the case of toxiferine Waser (1962) showed that the compound with two free hydroxyl groups had the highest action.…”
Section: General Properties Of the Relaxantssupporting
confidence: 71%
“…It may be seen from table I that dimethyltubocurarine 9.17 mg was needed per m 2 during 90 min, while tubocurarine 18.3 mg was needed under similar conditions (Stovner, Theodorsen and Bjelke, 1971a). This makes dimethyltubocurarine twice as potent as tubocurarine, a finding which is in good agreement with that of Wilson, Gordon and Raffan (1950). It is interesting that methyl substitution in tubocurarine has resulted in a compound with higher blocking activity, while in the case of toxiferine Waser (1962) showed that the compound with two free hydroxyl groups had the highest action.…”
Section: General Properties Of the Relaxantssupporting
confidence: 71%
“…Although metocurine has been available since its synthesis by King in 1935, it has not been popular in clinical use despite early studies suggesting less histamine release (Wilson, Gordon and Raffan, 1950) and little effect on arterial pressure (Stoelting, Graf and Vieira, 1948). More recent studies have confirmed the absence of significant autonomic effects both in animals (Hughes and Chappie, 1976a;Savarese, 1979) and man (Savarese, Ali and Antonio, 1977;Zaiden et al, 1977).…”
Section: Discussionmentioning
confidence: 99%