Elfazepam
Chemical compound
- none
- 7-Chloro-1-(2-ethylsulfonylethyl)-5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2-one
- 52042-01-0 Y
- 65445
- 58907 Y
- RM53R5R2BL
- DTXSID00200008
- Interactive image
- O=S(CC)(CCN1C(CN=C(C2=CC=CC=C2F)C3=C1C=CC(Cl)=C3)=O)=O
InChI
- InChI=1S/C19H18ClFN2O3S/c1-2-27(25,26)10-9-23-17-8-7-13(20)11-15(17)19(22-12-18(23)24)14-5-3-4-6-16(14)21/h3-8,11H,2,9-10,12H2,1H3 Y
- Key:BSPSXMXQKZZNFP-UHFFFAOYSA-N Y
Elfazepam[1] is a drug which is a benzodiazepine derivative.[2] Presumably it has sedative and anxiolytic actions like those of other benzodiazepines.
Orexigenic properties in animals.[3][4] The mechanism for increasing feed intake is not clear and has been subject of investigation.[5] It has been found that elfazepam suppresses gastric acid secretion.[6]
References
- ^ U.S. patent 4,010,154
- ^ Psychotropics.dk
- ^ Baile CA, McLaughlin CL (November 1979). "A review of the behavioral and physiological responses to elfazepam, a chemical feed intake stimulant". Journal of Animal Science. 49 (5): 1371–95. doi:10.2527/jas1979.4951371x. PMID 396294.
- ^ Baile CA, Naylor J, McLaughlin CL, Catanzaro CA (August 1981). "Endotoxin-elicited fever and anorexia and elfazepam-stimulated feeding in sheep". Physiology & Behavior. 27 (2): 271–7. doi:10.1016/0031-9384(81)90269-9. PMID 7029576. S2CID 12408796.
- ^ Keim DA, Baile CA, Bolton JR, Wangsness PJ, Della Fera MA (January 1979). "Abomasal function following injections of elfazepam and 9-aza-cannabinol". Pharmacology, Biochemistry, and Behavior. 10 (1): 63–70. doi:10.1016/0091-3057(79)90170-9. PMID 35793. S2CID 915512.
- ^ Van Den Broek GW, Robertson J, Keim DA, Baile CA (July 1979). "Feeding and depression of abomasal secretion in sheep elicited by elfazepam and 9-aza-cannabinol". Pharmacology, Biochemistry, and Behavior. 11 (1): 51–6. doi:10.1016/0091-3057(79)90296-x. PMID 493298. S2CID 33152825.
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Benzodiazepines
- 2-Oxoquazepam
- 3-Hydroxyphenazepam
- Bromazepam
- BMS-906024*
- Camazepam
- Carburazepam
- Chlordiazepoxide
- Cinazepam
- Cinolazepam
- Clonazepam
- Cloniprazepam
- Clorazepate
- Cyprazepam
- Delorazepam
- Demoxepam
- Desmethylflunitrazepam
- Devazepide*
- Diazepam
- Diclazepam
- Difludiazepam
- Doxefazepam
- Elfazepam
- Ethyl carfluzepate
- Ethyl dirazepate
- Ethyl loflazepate
- Flubromazepam
- Fletazepam
- Fludiazepam
- Flunitrazepam
- Flurazepam
- Flutemazepam
- Flutoprazepam
- Fosazepam
- Gidazepam
- Halazepam
- Iclazepam
- Irazepine*
- Kenazepine
- Ketazolam
- Lorazepam
- Lormetazepam
- Lufuradom*
- Meclonazepam
- Medazepam
- Menitrazepam
- Metaclazepam
- Motrazepam
- N-Desalkylflurazepam
- Nifoxipam
- Nimetazepam
- Nitemazepam
- Nitrazepam
- Nitrazepate
- Nordazepam
- Nortetrazepam
- Oxazepam
- Phenazepam
- Pinazepam
- Pivoxazepam
- Prazepam
- Proflazepam
- Quazepam
- QH-II-66
- Reclazepam
- RO4491533*
- Ro05-4082
- Ro5-4864*
- Ro07-5220
- Ro07-9749
- Ro20-8065
- Ro20-8552
- SH-I-048A
- Sulazepam
- Temazepam
- Tetrazepam
- Tifluadom*
- Timelotem*
- Tolufazepam
- Triflunordazepam
- Tuclazepam
- Uldazepam
* atypical activity profile (not GABAA receptor ligands)
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