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Iminostilbene

Miscellaneous. The iminostilbene carbama2epiae [294-46-4] congener of the tricycHc antidepressant, imipramine. [Pg.536]

Therapeutic Function Analgesic, Anticonvulsant Chemical Name 5H-dibenz[b,f] azepine-5-carboxamide Common Name 5-carbamyl iminostilbene Structural Formula ... [Pg.232]

C,4H 3N 494-/9-9) see Carpipramine Desipramine Imipramine Quinupramine Tiracizine Trimipramine 2-imino-a-phenyl>3-thiazolidineethanol (C H,4N20S 10060-88-5) see Levamisole iminostilbene... [Pg.2401]

A -Acyl derivatives of azepine like the iminostilbene 197 (Scheme 52) react in different ways depending on the nature of the N substituent if it is acyl, aroyl, or ethoxycarbonyl, the preferred reaction is dimerization on the other hand, N-tosyl compounds give PFR [154]. [Pg.91]

Carbamazepine is a tricyclic iminostilbene derivative and structurally related to the tricyclic antidepressants. It is used as a first-line agent for the management of generalized tonic-clonic epilepsy. It is also highly effective for partial seizures but has no efficacy in patients with absence seizures or atonic seizures. In epilepsy it supposedly has the same mechanism of action as phenytoin. An other well... [Pg.357]

Carbamazepine is an iminostilbene derivative used as an anticonvulsant and for the relief of pain associated... [Pg.312]

Iminostilbenes Carbamazepine (Tegretol) Oxcarbazepine (Trileptal) Similar to hydantoins... [Pg.108]

Ju C, Uetreeht JP. Detection of-2-hydroxy iminostilbene in the urine of patients taking carbamazepine and its oxidation to a reactive iminoquinone intermediate. J Pharmacol Exp Ther 1999 288 51-56. [Pg.703]

Fourteen seven-membered ring compounds have been tritium-labelled by AcT, AdT or HTI methods165 including ( )3,3,5-trimethylhexahydroazepine—162, 2-oxohex-amethyleneimine (caprolactam)—163, l-aza-2-methoxy-l-cycloheptene—164, 1,4-dia-zacycloheptane (homopiperazine)—165, l,8-diazabicyclo-[5.4.0]undec-7-ene—166, 5H-dibenzo[6j/]azepine (iminostilbene)—167, 8-chloro-l 1-(4-methyl-l-piperazinyl)5//-... [Pg.1168]

Gas Chromatography. System GA—carbamazepine RI 2290, carbamazepine-10,11-epoxide RI 2030, iminostilbene RI 1930 system GE—carbamazepine retention time 0.83 relative to phenytoin system GF—carbamazepine RI 2610, carbamazepine-10,11-epoxide RI 2560, iminostilbene RI 2620. [Pg.428]

Chemical/Pharmaceutical/Other Class Synthetic iminostilbene derivative structurally similar to imipramine, a tricyclic antidepressant. While unrelated structurally, carbamazepine shares a similar therapeutic action with phenytoin Chemical Formula C15H12N2O Chemical Structure ... [Pg.413]

See other pages where Iminostilbene is mentioned: [Pg.232]    [Pg.233]    [Pg.233]    [Pg.1514]    [Pg.821]    [Pg.663]    [Pg.279]    [Pg.618]    [Pg.621]    [Pg.106]    [Pg.107]    [Pg.109]    [Pg.111]    [Pg.821]    [Pg.822]    [Pg.822]    [Pg.822]    [Pg.428]    [Pg.1114]    [Pg.1118]    [Pg.1502]    [Pg.268]    [Pg.523]    [Pg.821]    [Pg.413]    [Pg.263]    [Pg.263]    [Pg.270]    [Pg.272]    [Pg.275]    [Pg.305]   
See also in sourсe #XX -- [ Pg.428 ]

See also in sourсe #XX -- [ Pg.152 ]

See also in sourсe #XX -- [ Pg.393 ]

See also in sourсe #XX -- [ Pg.234 ]

See also in sourсe #XX -- [ Pg.508 , Pg.547 , Pg.694 ]



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Iminostilbene Carbamazepine

Iminostilbene anticonvulsants

Iminostilbene derivatives

Iminostilbenes

Iminostilbenes

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