{"Abbreviation":"","Aliases":["Clorgiline","Chlorgyline","Clorgilina","Clorgilinum","M and B 9302","M \u0026 B 9302","N-(3-(2,4-Dichlorophenoxy)propyl)-N-methyl-2-propynylamine","M\u0026B 9302","N-(3-(2,4-dichlorophenoxy)propyl)-N-methylprop-2-yn-1-amine","2-Propyn-1-amine, N-(3-(2,4-dichlorophenoxy)propyl)-N-methyl-","Clorgilin","N-[3-(2,4-dichlorophenoxy)propyl]-N-methylprop-2-yn-1-amine","M\u0026B-9302","n-methyl-n-propargyl-3-(2,4-dichlorophenoxy)propylamine","2-Propynylamine, N-(3-(2,4-dichlorophenoxy)propyl)-N-methyl-","Cas-17780-75-5","Prestwick0_000344","Prestwick1_000344","Prestwick2_000344","Prestwick3_000344","Lopac-M-3778","Lopac0_000746","BSPBio_000407","US8633208, Clorgyline","SPBio_002328"],"CAS":"17780-72-2","ChEBI":"CHEBI:3763","ChEMBL":"CHEMBL8706","ChemicalClasses":["phenol"],"Chirality":"achiral","Classes":["Monoamine oxidase inhibitor"],"Erowid Experience Reports":null,"Esters":[],"Formating":[],"HMDB ID":"HMDB0250365","HeavyAtomCount":17,"IUPACName":"3-(2,4-dichlorophenoxy)-N-methyl-N-prop-2-ynylpropan-1-amine","InChI":"InChI=1S/C13H15Cl2NO/c1-3-7-16(2)8-4-9-17-13-6-5-11(14)10-12(13)15/h1,5-6,10H,4,7-9H2,2H3","InChIKey":"BTFHLQRNAMSNLC-UHFFFAOYSA-N","MeSH Pharmacological Classification":"Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems. (See all compounds classified as Antidepressive Agents.)","MolecularFormula":"C\u003csub\u003e13\u003c/sub\u003eH\u003csub\u003e15\u003c/sub\u003eCl\u003csub\u003e2\u003c/sub\u003eNO","MolecularWeight":"272.17 g/mol","PubChemId":4380,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Mirex","Name":"Clorgyline","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB04017","Name":"Clorgyline","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/4380","Name":"Clorgyline","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL8706","Name":"Clorgyline","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:3763","Name":"Clorgyline","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=17780-72-2","Name":"Clorgyline","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0250365","Name":"Clorgyline","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C11685","Name":"Clorgyline","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/LYJ16FZU9Q","Name":"Clorgyline","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID3048445","Name":"Clorgyline","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 4380, Clorgyline. Accessed July 20, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/4380\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/4380\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Clorgyline. UNII: LYJ16FZU9Q. Global Substance Registration System. Accessed July 20, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/LYJ16FZU9Q\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/LYJ16FZU9Q\u003c/a\u003e"],"SMILES":"CN(CCCOC1=C(C=C(C=C1)Cl)Cl)CC#C","SaltData":[{"AcidCount":1,"AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 97.601 148.792\"\u003e\u003crect width=\"100%\" height=\"100%\" fill=\"#fff\"/\u003e\u003cdesc\u003eGenerated by the Chemistry Development Kit (http://github.com/cdk)\u003c/desc\u003e\u003cg fill=\"#1ff01f\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h98v149H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m44.95 31.395 10.046 5.798M58.15 42.862l.002 11.391M58.152 54.253l-13.197 7.622M44.955 61.875l.002 15.24M44.957 77.115l-9.919 5.729M31.761 88.658l.002 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Effects":null,"Title":"Clorgyline","UNII":"LYJ16FZU9Q","Wikipedia":"Mirex","XLogP":4.2}