Jump to content

Tetronal: Difference between revisions

Page 1
Page 2
Content deleted Content added
BogBot (talk | contribs)
populated new fields in {{drugbox}} and reordered per bot approval. Report errors and suggestions to User_talk:BogBot
No edit summary
 
(14 intermediate revisions by 11 users not shown)
Line 1: Line 1:
{{Short description|Chemical compound}}
{{Drugbox
{{Drugbox
| verifiedrevid = 398759566
| verifiedrevid = 451222566
| IUPAC_name = 3,3-bis(ethylsulfonyl)pentane
| IUPAC_name = 3,3-bis(ethylsulfonyl)pentane
| image = Tetronal.svg
| image = Tetronal structure.svg
| width = 250
| width = 250


Line 10: Line 11:


<!--Identifiers-->
<!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 2217-59-6
| CAS_number = 2217-59-6
| PubChem = 75197
| PubChem = 75197
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 5XG2X0OW34
| ChemSpiderID = 67743


<!--Chemical data-->
<!--Chemical data-->
| C=9 | H=20 | O=4 | S=2
| C=9 | H=20 | O=4 | S=2
| molecular_weight = 256.383 g/mol
| smiles = CCC(CC)(S(=O)(=O)CC)S(=O)(=O)CC
| smiles = CCC(CC)(S(=O)(=O)CC)S(=O)(=O)CC
| StdInChI = 1S/C9H20O4S2/c1-5-9(6-2,14(10,11)7-3)15(12,13)8-4/h5-8H2,1-4H3
| StdInChIKey = VTZYVPLHCQBWSP-UHFFFAOYSA-N
}}
}}


'''Tetronal''' is a [[sedative-hypnotic]]<ref>(1907). [http://www.archive.org/stream/cu31924003469677#page/n453/mode/2up Merck's 1907 Index]. N. Y.: Merck & Co., p. 436.</ref> and [[anesthetic]] [[drug]] with [[GABAergic]] [[drug action|action]]s{{Citation needed|date=November 2010}}. It is not as effective as trional.<ref>Coblentz, Virgil (1908). [http://books.google.com/books?id=L3PtAAAAMAAJ&pg=PA123 The Newer Remedies]. Boston: Apothecary Publishing Co., p. 123.</ref>
'''Tetronal''' is a [[sedative-hypnotic]]<ref>{{cite book | date = 1907 | chapter-url = https://archive.org/stream/cu31924003469677#page/n453/mode/2up | chapter = Tetronal | title = Merck's 1907 Index | location = New York | publisher = Merck & Co. | page = 436 }}</ref> and [[anesthetic]] [[drug]] with [[GABAergic]] [[drug action|action]]s{{Citation needed|date=November 2010}}. It is not as effective as trional.<ref>{{cite book | vauthors = Coblentz V | date = 1908 | url = https://books.google.com/books?id=L3PtAAAAMAAJ&pg=PA123 | title = The Newer Remedies | location = Boston | publisher = Apothecary Publishing Co. | page = 123 }}</ref>


==History==
==History==
Tetronal was prepared and introduced by [[Eugen Baumann]] and [[Alfred Kast]] in 1888.<ref>Drinkwater, H. (1924). [http://www.archive.org/stream/fiftyyearsofmedi00drin#page/40/mode/2up Fifty years of medical progress, 1873-1922]. New York: The Macmillan Company, p. 40.</ref>
Tetronal was introduced by [[Eugen Baumann]] and [[Alfred Kast]] in 1888.<ref>{{cite book | vauthors = Drinkwater H | date = 1924 | url = https://archive.org/stream/fiftyyearsofmedi00drin#page/40/mode/2up | title = Fifty years of medical progress, 1873-1922 | location = New York | publisher = The Macmillan Company | page = 40 }}</ref>


==See also==
==See also==
Line 29: Line 35:


==References==
==References==
{{Reflist|2}}
{{Reflist}}


{{Hypnotics}}
{{Hypnotics}}
{{General anesthetics}}
{{General anesthetics}}
{{GABAergics}}
{{GABAAR PAMs}}
{{GABAAergics}}


[[Category:Hypnotics]]
[[Category:Hypnotics]]
[[Category:Sulfones]]
[[Category:Sulfones]]
[[Category:GABAA receptor positive allosteric modulators]]




{{nervous-system-drug-stub}}
{{sedative-stub}}