Flopropione: Difference between revisions

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Updating {{drugbox}} (no changed fields - added verified revid - updated 'ChemSpiderID_Ref', 'DrugBank_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref', 'DrugBank_Ref', 'ChEBI_Ref') per [[Wikipedia:WikiProject Chemicals/Chembox vali
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{{Short description|Spasmolytic or antispasmodic agent}}
{{drugbox
{{Drugbox
| Verifiedfields = changed
| verifiedrevid = 444212589
| IUPAC_name = 1-(2,4,6-trihydroxyphenyl)propan-1-one
| image = Flopropione.svg

<!--Clinical data-->
| tradename =
| Drugs.com = {{drugs.com|international|flopropione}}
| pregnancy_category =
| legal_status =
| routes_of_administration = Oral

<!--Pharmacokinetic data-->
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =

<!--Identifiers-->
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 2295-58-1
| ATC_prefix = none
| ATC_suffix =
| PubChem = 3362
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 05V5NVB5Y1
| UNII = 05V5NVB5Y1
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| verifiedrevid = 437131682
| ChEMBL = 1605835
| IUPAC_name = 1-(2,4,6-trihydroxyphenyl)propan-1-one
| image = Flopropione.svg
| CAS_number = 2295-58-1
| ATC_prefix = none
| ATC_suffix =
| PubChem = 3362
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D01259
| KEGG = D01259
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| C = 9 | H = 10 | O = 4
| ChemSpiderID = 3245
| molecular_weight = 182.17 g/mol
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| smiles = CCC(=O)C1=C(C=C(C=C1O)O)O
| StdInChI = 1S/C9H10O4/c1-2-6(11)9-7(12)3-5(10)4-8(9)13/h3-4,10,12-13H,2H2,1H3
| bioavailability =
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| protein_bound =
| metabolism =
| StdInChIKey = PTHLEKANMPKYDB-UHFFFAOYSA-N
| DrugBank =
| elimination_half-life =

| excretion =
<!--Chemical data-->
| pregnancy_category=
| legal_status =
| C=9 | H=10 | O=4
| smiles = CCC(=O)C1=C(C=C(C=C1O)O)O
| routes_of_administration = Oral
}}
}}


'''Flopropione''' ('''Compacsul''', '''Cospanon''', '''Ecapron''', '''Pellegal''', '''Argobyl''', '''Floveton''', '''Saritron''', '''Spamorin''', '''Labrodax''', '''Tryalon''', '''Mirulevatin''', '''Padeskin''', '''Profenon''') is a [[muscle relaxant#Spasmolytics|spasmolytic]] or [[antispasmodic]] agent.<ref name="urlDictionary of Organic Compounds ... - Google Books">{{cite web | url = http://books.google.com/books?id=kfhQgpqxiVgC&lpg=PA1&dq=flopropione&as_brr=3&pg=PA241#v=onepage&q=flopropione&f=false | title = Dictionary of Organic Compounds ... - Google Books | format = | work = | accessdate = }}</ref> It acts as a [[5-HT1A receptor|5-HT<sub>1A</sub> receptor]] [[receptor_antagonist|antagonist]].<ref name="urlDictionary of Organic Compounds ... - Google Books">{{cite web | url = http://books.google.com/books?id=kfhQgpqxiVgC&lpg=PA1&dq=flopropione&as_brr=3&pg=PA241#v=onepage&q=flopropione&f=false | title = Dictionary of Organic Compounds ... - Google Books | format = | work = | accessdate = }}</ref>
'''Flopropione''' ('''Compacsul''', '''Cospanon''', '''Ecapron''', '''Pellegal''', '''Argobyl''', '''Floveton''', '''Saritron''', '''Spamorin''', '''Labrodax''', '''Tryalon''', '''Mirulevatin''', '''Padeskin''', '''Profenon''') is a [[muscle relaxant#Spasmolytics|spasmolytic]] or [[antispasmodic]] agent.<ref name="urlDictionary of Organic Compounds ... - Google Books">{{cite book | url = https://books.google.com/books?id=kfhQgpqxiVgC&q=flopropione&pg=PA241 | title = Dictionary of Organic Compounds ... - Google Books | isbn = 978-0-412-54110-0 | vauthors = Buckingham J, MacDonald F | date = 26 September 1996 }}</ref> It acts as a [[COMT]] [[inhibitory postsynaptic potential|inhibitor]].<ref name="Cospanon">{{cite web | url = http://eisai.jp/medical/products/di/EPI/CSP_C_EPI.pdf | title = Cospanon label | access-date = 2016-03-14 | archive-date = 2016-10-07 | archive-url = https://web.archive.org/web/20161007001057/http://eisai.jp/medical/products/di/EPI/CSP_C_EPI.pdf | url-status = dead }}</ref>


It is synthesized from [[phloroglucinol]] in a [[Hoesch reaction]].

==See also==
*[[2,4,6-Trihydroxyacetophenone]] (THAP)
== References ==
== References ==
{{Reflist|2}}
{{Reflist}}



{{Muscle relaxants}}
{{Muscle relaxants}}
{{Serotonergics}}
{{Serotonergics}}


[[Category:Phloroglucinols]]


[[Category:Synthetic phloroglucinols]]
[[Category:Aromatic ketones]]
[[Category:Aromatic ketones]]
[[Category:Serotonin receptor antagonists]]

[[Category:3-Hydroxypropenals]]


{{musculoskeletal-drug-stub}}
{{musculoskeletal-drug-stub}}