Hexapropymate
Chemical compound
- N05CM10 (WHO)
- 1-prop-2-yn-1-ylcyclohexyl carbamate
- 358-52-1
Y
- 9661
- 9280
N
- 0J9RN2PRJ7
- ChEMBL2104292
N
- DTXSID00189329
![Edit this at Wikidata](http://upload.wikimedia.org/wikipedia/en/thumb/8/8a/OOjs_UI_icon_edit-ltr-progressive.svg/10px-OOjs_UI_icon_edit-ltr-progressive.svg.png)
- Interactive image
- O=C(OC1(CCCCC1)CC#C)N
InChI
- InChI=1S/C10H15NO2/c1-2-6-10(13-9(11)12)7-4-3-5-8-10/h1H,3-8H2,(H2,11,12)
N
- Key:MIRHIEAGDGUXKL-UHFFFAOYSA-N
N
![☒](http://upload.wikimedia.org/wikipedia/commons/thumb/a/a2/X_mark.svg/7px-X_mark.svg.png)
![check](http://upload.wikimedia.org/wikipedia/en/thumb/f/fb/Yes_check.svg/7px-Yes_check.svg.png)
Hexapropymate is a hypnotic/sedative. It has effects similar to those of barbiturates and was used in the 1970s-1980s in the treatment of insomnia before being replaced with newer drugs with improved safety profiles.[1]
References
- ^ Gustafsson LL, Berg A, Magnusson A, Malmlund HO, Sandell BM, Stig R (1989). "Hexapropymate self-poisoning causes severe and long-lasting clinical symptoms". Medical Toxicology and Adverse Drug Experience. 4 (4): 295–301. doi:10.1007/bf03259914. PMID 2770531. S2CID 24560026.
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Hypnotics/sedatives (N05C)
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