Acetylglycinamide chloral hydrate: Difference between revisions
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{{Short description|Chemical compound}} |
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{{drugbox |
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{{Drugbox |
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| IUPAC_name = |
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| image = Acetylglycinamide chloral hydrate.PNG |
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| verifiedrevid = 447909838 |
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| type = combo |
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| component1 = N-Acetylglycinamide |
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| PubChem = |
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| class1 = [[glycine]] derivative |
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| class2 = [[sedative]]/[[hypnotic]] |
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| tradename = |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 6WZ3595RLZ |
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| PubChem = 71587019 |
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'''Acetylglycinamide chloral hydrate''' is a [[hypnotic]]/[[sedative]]. |
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'''Acetylglycinamide chloral hydrate''' is a [[hypnotic]]/[[sedative]]. It is a combination of [[N-Acetylglycinamide|acetylglycinamide]] and [[chloral hydrate]].<ref>{{cite journal | vauthors = Degerholm E, Harison A, Leideman T, Sterner N | title = Acetylglycinamide chloral hydrate, a new compound | journal = Farmacevtisk Revy | year = 1963 | volume = 62 | issue = 29 | pages = 601–611}}</ref> |
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==Systematic Names:== |
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* N-(2-amino-2-oxoethyl)acetamide, compd. with 2,2,2-trichloroethanol ([Chloral hydrate]] |
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==References== |
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{{reflist}} |
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* AGAK |
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==See also== |
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{{GABAAR PAMs}} |
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* [[N-acetylglycinamide]] |
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[[Category:Sedatives]] |
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[[Category:Combination drugs]] |
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[[Category:GABAA receptor positive allosteric modulators]] |
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==External links== |
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* http://bioinformatics.charite.de/superligands/drug_similarity.php?hetero=MSE |
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* PubChem: [http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?sid=11456731 2-amino-2-ethoxyacetamide] |
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{{sedative-stub}} |
{{sedative-stub}} |
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Latest revision as of 14:08, 14 February 2021
Combination of | |
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N-Acetylglycinamide | glycine derivative |
Chloral hydrate | sedative/hypnotic |
Clinical data | |
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PubChem CID | |
UNII | |
CompTox Dashboard (EPA) | |
(verify) |
Acetylglycinamide chloral hydrate is a hypnotic/sedative. It is a combination of acetylglycinamide and chloral hydrate.[1]
References
[edit]- ^ Degerholm E, Harison A, Leideman T, Sterner N (1963). "Acetylglycinamide chloral hydrate, a new compound". Farmacevtisk Revy. 62 (29): 601–611.