Flopropione: Difference between revisions
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{{Short description|Spasmolytic or antispasmodic agent}} |
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{{Drugbox |
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<!--Clinical data--> |
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| Drugs.com = {{drugs.com|international|flopropione}} |
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<!--Pharmacokinetic data--> |
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<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 05V5NVB5Y1 |
| UNII = 05V5NVB5Y1 |
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| ChEMBL_Ref = {{ebicite|changed|EBI}} |
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| ChEMBL = 1605835 |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = D01259 |
| KEGG = D01259 |
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| ChemSpiderID = 3245 |
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| molecular_weight = 182.17 g/mol |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChI = 1S/C9H10O4/c1-2-6(11)9-7(12)3-5(10)4-8(9)13/h3-4,10,12-13H,2H2,1H3 |
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| StdInChIKey = PTHLEKANMPKYDB-UHFFFAOYSA-N |
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<!--Chemical data--> |
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| C=9 | H=10 | O=4 |
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'''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 |
'''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> |
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It is synthesized from [[phloroglucinol]] in a [[Hoesch reaction]]. |
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==See also== |
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*[[2,4,6-Trihydroxyacetophenone]] (THAP) |
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== References == |
== References == |
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{{Reflist |
{{Reflist}} |
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{{Muscle relaxants}} |
{{Muscle relaxants}} |
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{{Serotonergics}} |
{{Serotonergics}} |
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[[Category:Phloroglucinols]] |
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[[Category:Synthetic phloroglucinols]] |
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[[Category:Aromatic ketones]] |
[[Category:Aromatic ketones]] |
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[[Category:Serotonin receptor antagonists]] |
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[[Category:3-Hydroxypropenals]] |
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{{musculoskeletal-drug-stub}} |
{{musculoskeletal-drug-stub}} |