Beclamide (original) (raw)

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Chemical compound

Pharmaceutical compound

Beclamide

Clinical data
Routes of administration By mouth
ATC code N03AX30 (WHO)
Legal status
Legal status BR: Class C1 (Other controlled substances)[1]
Identifiers
IUPAC name _N_-Benzyl-3-chloropropanamide
CAS Number 501-68-8 checkY
PubChem CID 10391
ChemSpider 9962 checkY
UNII F5N0ALI65V
KEGG D07300 checkY
ChEMBL ChEMBL64195 checkY
CompTox Dashboard (EPA) DTXSID5057755 Edit this at Wikidata
ECHA InfoCard 100.007.207 Edit this at Wikidata
Chemical and physical data
Formula C10H12ClNO
Molar mass 197.66 g·mol−1
3D model (JSmol) Interactive image
Melting point 94 °C (201 °F)
SMILES ClCCC(=O)NCc1ccccc1
InChI InChI=1S/C10H12ClNO/c11-7-6-10(13)12-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,12,13) checkYKey:JPYQFYIEOUVJDU-UHFFFAOYSA-N checkY
(verify)

Beclamide (marketed as Chloracon, Hibicon, Posedrine, Nydrane, Seclar, and other names) is a drug that possesses anticonvulsant activity.[2] It is no longer used.

It has been used as a sedative and as an anticonvulsant.

It was studied in the 1950s for its anticonvulsant properties, as a treatment for generalised tonic-clonic seizures. It was not effective for absence seizures.

Interest in the drug resumed in the 1990s for its psychiatric properties as an adjunct in the treatment of schizophrenia.[3]

Side effects are uncommon but include stomach pain, nervousness, giddiness, skin rash and leukopenia. It is counter-indicated in breast feeding as it is passed in the milk.

  1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  2. ^ Ahmadi M, Nicholls PJ, Smith HJ, Spencer PS, Preet-Ryatt MS, Spragg BP (October 1995). "Metabolism of beclamide after a single oral dose in man: quantitative studies". The Journal of Pharmacy and Pharmacology. 47 (10): 876–8. doi:10.1111/j.2042-7158.1995.tb05757.x. PMID 8583359. S2CID 19556266.
  3. ^ Raptis C, Garcia-Borreguero D, Weber MM, Dose M, Bremer D, Emrich HM (February 1990). "Anticonvulsants as adjuncts for the neuroleptic treatment of schizophrenic psychoses: a clinical study with beclamide". Acta Psychiatrica Scandinavica. 81 (2): 162–7. doi:10.1111/j.1600-0447.1990.tb06472.x. PMID 2183543. S2CID 26772370.