{"Aliases":["IP 456","Pagoclona","RP-62955","IP-456","CI-1043","RP 62955","2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)-2,3-dihydro-1H-isoindol-1-one","IP456","RP62955","38VAG2SA33","pagoclonum","Dtxcid90817740","2-(7-chloro-1.8-naphthyridin-2-yl)-2,3-dihydro-3-(5-methyl-2-oxohexyl)-1H-isoindol-1-one","133737-48-1","rac-Pagoclone","2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)isoindolin-1-one","RP-59037","2-(7-Chloro-1,8-naphthyridin-2-yl)-2,3-dihydro-3-(5-methyl-2-oxohexyl)-1H-isoindol-1-one; RP 59037; IP 456; RP 62955","Mfcd00864700","RP 59037","Mls006010289","Schembl449997","Chembl2104745","Schembl14336500","Schembl29556669","EX-A896","1H-Isoindol-1-one, 2-(7-chloro-1,8-naphthyridin-2-yl)-2,3-dihydro-3-(5-methyl-2-oxohexyl)-, (+)-","2-(7-Chloro-2-naphthyridin-1,8-yl)-3-(5-methyl-2-oxohexyl)isoindolin-1-one","Akos015960516","CI 1043","CS-6427","DB04903","SB17133","Ncgc00386587-01","AC-36822","BP177437","DA-45926","Smr004701358","HY-101665","D02616","2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)-1-isoindolinone","2-(7-Chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)phthalimidine","2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxo-hexyl)isoindolin-1-one","racemic-2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxo-hexyl)-1-isoindolinone","1H-Isoindol-1-one, 2-(7-chloro-1,8-naphthyridin-2-yl)-2,3-dihydro-3-(5-methyl-2-oxohexyl)-","2-(7-chloro-1,8-naphthyridin-2-yl)-2,3-dihydro-3-(5-methyl-2-oxohexyl)-1H-isoindol-1-one"],"CAS":"133737-32-3","ChemicalClasses":["cyclopyrrolone"],"Chirality":"racemic","DTXSID":"40869830","Drug Indication":"For the potential treatment of panic and anxiety disorders.","Druglikeness":{"Lipinski":{"Passes":true,"Violations":1}},"EliminationHalfLife":"","Erowid Experience Reports":[],"Esters":[],"Formating":[],"HeavyAtomCount":29,"IUPACName":"2-(7-chloro-1,8-naphthyridin-2-yl)-3-(5-methyl-2-oxohexyl)-3H-isoindol-1-one","InChI":"InChI=1S/C23H22ClN3O2/c1-14(2)7-10-16(28)13-19-17-5-3-4-6-18(17)23(29)27(19)21-12-9-15-8-11-20(24)25-22(15)26-21/h3-6,8-9,11-12,14,19H,7,10,13H2,1-2H3","InChIKey":"HIUPRQPBWVEQJJ-UHFFFAOYSA-N","MeSH Headers":[{"Id":"M0415264","Link":"https://id.nlm.nih.gov/mesh/M0415264.html","Name":"pagoclone","Ref":23},{"Id":"M0415266","Link":"https://id.nlm.nih.gov/mesh/M0415266.html","Name":"RP 62955","Ref":24},{"Id":"DescTree","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":"MeSH Tree","Ref":25},{"Id":"PubMed from MeSH","Link":"https://www.nlm.nih.gov/mesh/meshhome.html","Name":null,"Ref":35}],"Mechanism of Action":"Pagoclone is a subtype-selective drug which binds primarily to the alpha2/alpha3 subtypes of the GABAA receptor which are responsible for the anti-anxiety effects of these kind of drugs, but has relatively little efficacy at the alpha1 subtype which produces the sedative and memory loss effects.","MolecularFormula":"C\u003csub\u003e23\u003c/sub\u003eH\u003csub\u003e22\u003c/sub\u003eClN\u003csub\u003e3\u003c/sub\u003eO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"407.9 g/mol","Passes":true,"Pharmacodynamics":"Pagoclone was originally developed as an anti-anxiety drug, but never commercialised. It is a partial agonist acting at GABAA receptors in the brain. In contrast to zopiclone, pagoclone produces anxiolytic effects with little or no sedative or amnestic actions at low doses.","PubChemId":131664,"PubChemTitle":"Pagoclone","RefChem":"858293","RefCount":2,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Pagoclone","Name":"Pagoclone","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q7124393","Name":"Pagoclone","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/DB04903","Name":"Pagoclone","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/131664","Name":"Pagoclone","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=133737-32-3","Name":"Pagoclone","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/D02616","Name":"Pagoclone","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID40869830","Name":"Pagoclone","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 131664, Pagoclone. 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