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{{Short description|Chemical compound}} |
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{{drugbox |
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{{Drugbox |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| Verifiedfields = changed |
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| UNII = 5ML58O200F |
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| Watchedfields = changed |
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| verifiedrevid = 437147957 |
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| verifiedrevid = 451225156 |
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| IUPAC_name = (E)-3-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylprop-2-en-1-one |
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| IUPAC_name = (2''E'')-3-(2''H''-1,3-Benzodioxol-5-yl)-1-(piperidin-1-yl)prop-2-en-1-one |
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| image = Ilepcimide.png |
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| image = Ilepcimide.png |
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| width = 200px |
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| width = 200px |
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| CAS_number = 23434-86-8 |
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<!--Clinical data--> |
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<!--Pharmacokinetic data--> |
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<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|correct|??}} |
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| CAS_number = 82857-82-7 |
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| ATC_prefix = none |
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| ATC_prefix = none |
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| ATC_suffix = |
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| PubChem = 641115 |
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| PubChem = 641115 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| C = 15 | H = 17 | N = 1 | O = 3 |
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| UNII = 5ML58O200F |
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| molecular_weight = 259.300 g/mol |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = 556435 |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChI = 1S/C15H17NO3/c17-15(16-8-2-1-3-9-16)7-5-12-4-6-13-14(10-12)19-11-18-13/h4-7,10H,1-3,8-9,11H2/b7-5+ |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = BLPUOQGPBJPXRL-FNORWQNLSA-N |
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<!--Chemical data--> |
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| C=15 | H=17 | N=1 | O=3 |
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| smiles = C1CCN(CC1)C(=O)/C=C/C2=CC3=C(C=C2)OCO3 |
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| smiles = C1CCN(CC1)C(=O)/C=C/C2=CC3=C(C=C2)OCO3 |
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}} |
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}} |
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'''Ilepcimide''', also known as '''antiepilepserine''', is an ].<ref name="GanellinTriggle1996">{{cite book | vauthors = Ganellin CR, Triggle DJ | title = Dictionary of Pharmacological Agents | url = https://books.google.com/books?id=A0THacd46ZsC&pg=PA1116 | accessdate = 30 November 2012 | date = 21 November 1996 | publisher = CRC Press | isbn = 978-0-412-46630-4 | page = 1116}}</ref> It is a ] ] that was first synthesized by Chinese researchers as an ] of ], the main pungent compound and ] of ] (and of other plants in the family ]). |
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'''Ilepcimide''' ('''Antiepilepserine''') is a ] ] used in ]. |
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Ilepcimide has ] activity.<ref name="GanellinTriggle1996" /><ref>{{cite journal | vauthors = Liu GQ, Algeri S, Ceci A, Garattini S, Gobbi M, Murai S | title = Stimulation of serotonin synthesis in rat brain after antiepilepsirine, an antiepileptic piperine derivative | journal = Biochemical Pharmacology | volume = 33 | issue = 23 | pages = 3883–6 | date = December 1984 | pmid = 6210090 | doi = 10.1016/0006-2952(84)90055-8 | doi-access = free }}</ref><ref>{{cite journal | vauthors = Yan QS, Mishra PK, Burger RL, Bettendorf AF, Jobe PC, Dailey JW | title = Evidence that carbamazepine and antiepilepsirine may produce a component of their anticonvulsant effects by activating serotonergic neurons in genetically epilepsy-prone rats | journal = The Journal of Pharmacology and Experimental Therapeutics | volume = 261 | issue = 2 | pages = 652–9 | date = May 1992 | pmid = 1374472 }}</ref> |
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==See also== |
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* ] |
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== References == |
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== References == |
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{{Anticonvulsants}} |
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{{Anticonvulsants}} |
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