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1 References  














Amiphenazole






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Amiphenazole

Clinical data

ATC code

  • none

Legal status

Legal status

  • AU: S4 (Prescription only)

Identifiers

  • 5-phenyl-1,3-thiazole-2,4-diamine

CAS Number

PubChem CID

ChemSpider

UNII

ChEMBL

CompTox Dashboard (EPA)

ECHA InfoCard

100.007.013 Edit this at Wikidata

Chemical and physical data

Formula

C9H9N3S

Molar mass

191.25 g·mol−1

3D model (JSmol)

  • C1=CC=C(C=C1)C2=C(N=C(S2)N)N

  • InChI=1S/C9H9N3S/c10-8-7(13-9(11)12-8)6-4-2-1-3-5-6/h1-5H,10H2,(H2,11,12) checkY

  • Key:UPOYFZYFGWBUKL-UHFFFAOYSA-N checkY

  •   (verify)

    Amiphenazole (Daptazile) is a respiratory stimulant traditionally used as an antidote for barbiturateoropiate overdose, usually in combination with bemegride,[1][2] as well as poisoning from other sedative drugs[3][4] and treatment of respiratory failure from other causes.[5] It was considered particularly useful as it could counteract the sedation and respiratory depression produced by morphine but with less effect on analgesia.[6][7] It is still rarely used in medicine in some countries, although it has largely been replaced by more effective respiratory stimulants such as doxapram and specific opioid antagonists such as naloxone.[8][9]

    References[edit]

    1. ^ Worlock A (November 1956). "Barbiturate poisoning treated with amiphenazole and bemegride". British Medical Journal. 2 (5001): 1099–101. doi:10.1136/bmj.2.5001.1099. PMC 2035840. PMID 13364395.
  • ^ Mears GW (March 1958). "Massive doses of bemegride and amiphenazole in treatment of barbiturate poisoning". British Medical Journal. 1 (5073): 757–8. doi:10.1136/bmj.1.5073.757. PMC 2028148. PMID 13510792.
  • ^ Dotevall G, Herner B (August 1957). "Treatment of acute primidone poisoning with bemegride and amiphenazole". British Medical Journal. 2 (5042): 451–2. doi:10.1136/bmj.2.5042.451. PMC 1961943. PMID 13446511.
  • ^ Rowell NR (February 1957). "Treatment of glutethimide poisoning with bemegride and amiphenazole". Lancet. 272 (6965): 407–9. doi:10.1016/s0140-6736(57)90466-x. PMID 13407028.
  • ^ Little GM (January 1962). "Use of amiphenazole in respiratory failure". British Medical Journal. 1 (5273): 223–6. doi:10.1136/bmj.1.5273.223. PMC 1957266. PMID 14465883.
  • ^ Mckeogh J, Shaw FH (January 1956). "Further experience with amiphenazole and morphine in intractable pain". British Medical Journal. 1 (4959): 142–4. doi:10.1136/bmj.1.4959.142. PMC 1978927. PMID 13276651.
  • ^ Gershon S, Bruce DW, Orchard N, Shaw FH (August 1958). "Amiphenazole and morphine in production of analgesia". British Medical Journal. 2 (5092): 366–8. doi:10.1136/bmj.2.5092.366. PMC 2025982. PMID 13560868.
  • ^ Gairola RL, Gupta PK, Pandley K (January 1980). "Antagonists of morphine-induced respiratory depression. A study in postoperative patients". Anaesthesia. 35 (1): 17–21. doi:10.1111/j.1365-2044.1980.tb03714.x. PMID 6994518. S2CID 40955560.
  • ^ O'Neill WM (1994). "The cognitive and psychomotor effects of opioid drugs in cancer pain management". Cancer Surveys. 21: 67–84. PMID 8565000.
  • Other respiratory system products (R07)

    Lung surfactants

  • Dipalmitoylphosphatidylcholine
  • Respiratory stimulants

  • Amiphenazole
  • Bemegride
  • Dimefline
  • Doxapram
  • Etamivan
  • GAL-021
  • Mepixanox
  • Nikethamide
  • Pentetrazol
  • Prethcamide
  • 5-HT4 receptor agonists

  • Zacopride
  • Other agents for treating respiratory depression

  • Nitric oxide
  • BW373U86
  • CX-546
  • CX-717
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Amiphenazole&oldid=1194712076"

    Categories: 
    Drugs not assigned an ATC code
    Antidotes
    Stimulants
    Respiratory agents
    Thiazoles
    World Anti-Doping Agency prohibited substances
    Respiratory system drug stubs
    Hidden categories: 
    Articles with short description
    Short description matches Wikidata
    ECHA InfoCard ID from Wikidata
    Chemical pages without DrugBank identifier
    Articles without KEGG source
    All stub articles
     



    This page was last edited on 10 January 2024, at 10:24 (UTC).

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