U-90042
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| Systematic (IUPAC) name | |
| 11-Chloro-5-(5-cyclopropyl-1,2,4-oxadiazol-3-yl)-2,3-dihydrodiimidazo[1,2-c:1',5'-a]quinazoline | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | ? |
| Identifiers | |
| CAS number | 134516-99-7 |
| ATC code | ? |
| PubChem | CID 9928470 |
| Chemical data | |
| Formula | C17H13ClN6O |
| Mol. mass | 352.78 g/mol |
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U-90042 is a sedative and hypnotic drug used in scientific research. It has similar effects to sedative-hypnotic benzodiazepine drugs, but is structurally distinct and so is classed as a nonbenzodiazepine hypnotic.
U-90042 is a GABAA agonist acting primarily at the α1, α3 and α6 subtypes, with a Ki of 7.8nM at α1, 9.5nM at α3 and 11.0nM at α6. It produces sedation and ataxia and prolongs sleeping time in mice, rats and monkeys, but does not produce amnesia and blocks the amnestic effect of diazepam, reflecting its different subtype affinity compared to benzodiazepine drugs.[1] It was developed by a team at Novo Nordisk in the 1980s.[2]
References [edit]
- ^ Tang, AH; Smith, MW; Carter, DB; Im, WB; Vonvoigtlander, PF (1995). "U-90042, a sedative/hypnotic compound that interacts differentially with the GABAA receptor subtypes". The Journal of Pharmacology and Experimental Therapeutics 275 (2): 761–7. PMID 7473164.
- ^ US Patent 5100895 Heterocyclic compounds and their preparation and use
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