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词条 NS-2664
释义

  1. References

{{Drugbox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 424949355
| IUPAC_name = 5-furan-3-yl-1-(3-imidazol-1-yl-phenyl)-1H-benzoimidazole
| image = NS-2664.png
| tradename =
| pregnancy_AU =
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| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
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| routes_of_administration =
| bioavailability =
| protein_bound =
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| PubChem = 9840300
| DrugBank =
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 8016018
| C=20 | H=14 | N=4 | O=1
| molecular_weight = 326.351 g/mol
| smiles = c5occc5-c(cc1nc4)ccc1n4-c2cc(ccc2)-n3cncc3
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C20H14N4O/c1-2-17(23-8-7-21-13-23)11-18(3-1)24-14-22-19-10-15(4-5-20(19)24)16-6-9-25-12-16/h1-14H
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = QMKRPSVBKKEAKS-UHFFFAOYSA-N
}}NS-2664 (LS-193,048) is an anxiolytic drug with a novel chemical structure, developed by the small pharmaceutical company NeuroSearch. It has similar effects to benzodiazepine drugs, but is structurally distinct and so is classed as a nonbenzodiazepine anxiolytic. NS-2664 is a potent but non-selective partial agonist at GABAA receptors, although with little efficacy at the α1 subtype and more at α2 and α3. It has potent anticonvulsant effects in animal studies, but a relatively short duration of action, and produces little sedative effects or physical dependence.[1]

References

1. ^Mirza NR, Nielsen EØ. Do subtype-selective gamma-aminobutyric acid A receptor modulators have a reduced propensity to induce physical dependence in mice? Journal of Pharmacology and Experimental Therapeutics. 2006 Mar;316(3):1378-85. {{PMID|16352707}}
{{Anxiolytics}}{{GABAAR PAMs}}{{nervous-system-drug-stub}}

5 : Anxiolytics|Furans|Benzimidazoles|Imidazoles|GABAA receptor positive allosteric modulators

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