Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Cyclarbamate

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Cyclarbamate
Clinical data
Other namesBSM-906M
ATC code
  • None
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Identifiers
  • Cyclopentane-1,1-diyldimethanediyl bis(phenylcarbamate)
CAS Number
PubChemCID
ChemSpider
UNII
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.024.821Edit this at Wikidata
Chemical and physical data
FormulaC21H24N2O4
Molar mass368.433 g·mol−1
3D model (JSmol)
  • O=C(OCC1(CCCC1)COC(=O)Nc2ccccc2)Nc3ccccc3
  • InChI=1S/C21H24N2O4/c24-19(22-17-9-3-1-4-10-17)26-15-21(13-7-8-14-21)16-27-20(25)23-18-11-5-2-6-12-18/h1-6,9-12H,7-8,13-16H2,(H,22,24)(H,23,25)
  • Key:IRZVVDMCEZNNCW-UHFFFAOYSA-N

Cyclarbamate (INN;Casmalon), also known ascyclopentaphene, is amuscle relaxant andtranquilizer of thecarbamate family which has been marketed byCassenne inFrance since 1961.[2][3][4]

References

[edit]
  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. Retrieved2023-08-16.
  2. ^William Andrew Publishing (2007).Pharmaceutical manufacturing encyclopedia. Elsevier. p. 1155.ISBN 978-0-8155-1526-5. Retrieved26 November 2011.
  3. ^World Health Organization (2004)."The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substance"(PDF).
  4. ^Gaultier M, Leperchey F (April 1962). "[Preliminary data on the use in clinical practice of cyclarbamate (N,N-diphenyl dicarbamate of 1,1-cyclopentanedimethanol]".La Presse Médicale (in French).70:863–4.PMID 13897295.


Peripherally acting
(primarilyantinicotinic,
NMJ block)
Non-depolarizing
Curarealkaloids
4° ammonium agents
Depolarizing
ACh release inhibitors
Centrally acting
Carbamic acid esters
Benzodiazepines
Nonbenzodiazepines
Thienodiazepines
Quinazolines
Anticholinergics
(Antimuscarinics)
Other
Directly acting
GABAA
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Imidazoles
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Quinazolinones
Others
GABAB
H1
Antihistamines
Antidepressants
Antipsychotics
α2-Adrenergic
5-HT2A
Antidepressants
Antipsychotics
Others
Melatonin
Orexin
α2δVDCC
Others
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
Retrieved from "https://en.wikipedia.org/w/index.php?title=Cyclarbamate&oldid=1268907279"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp