{"ATC Code":"N - Nervous system","Abbreviation":[],"Aliases":["Sultopridum","Sultoprida","N-((1-Ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-o-anisamide","Benzamide, N-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxy-","N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxy-benzamide","N-((1-ethylpyrrolidin-2-yl)methyl)-5-ethylsulfonyl-2-methoxy-benzamide","RefChem:890031","N05AL02","N-(Ethyl-1-pyrrolidinyl-2-methyl)methoxy-2-ethylsulfonyl-5-benzamide","258-641-9","Barnetil","Topral","LIN 1418","LIN-1418","Sultroprida","N-((1-ethylpyrrolidin-2-yl)methyl)-5-(ethylsulfonyl)-2-methoxybenzamide","Ncgc00185771-01","N-((1-ethyl-2-pyrrolidinyl)methyl)-5-(ethylsulfonyl)-2-methoxybenzamide","5-22-08-00103","orb1685514","KXB00443","Pdsp1_001575","Pdsp2_001559","o-ANISAMIDE, N-((1-ETHYL-2-PYRROLIDINYL)METHYL)-5-(ETHYLSULFONYL)-","DB13273"],"CAS":"53583-79-2","ChEBI":"CHEBI:9356","ChEMBL":"CHEMBL277945","ChemicalClasses":["benzylamine"],"Chirality":"racemic","Drug Classes":"Breast Feeding; Lactation; Milk, Human; Antipsychotic Agents; Dopamine Antagonists","EINECS":"258-641-9","EliminationHalfLife":"3 – 5 hours","Esters":[],"European Community (EC) Number":"258-641-9","Formating":[],"HMDB ID":"HMDB0258623","HeavyAtomCount":24,"Human Drugs":"Breast Feeding; Lactation; Milk, Human; Antipsychotic Agents; Dopamine Antagonists","IUPACName":"N-[(1-ethylpyrrolidin-2-yl)methyl]-5-ethylsulfonyl-2-methoxybenzamide","InChI":"InChI=1S/C17H26N2O4S/c1-4-19-10-6-7-13(19)12-18-17(20)15-11-14(24(21,22)5-2)8-9-16(15)23-3/h8-9,11,13H,4-7,10,12H2,1-3H3,(H,18,20)","InChIKey":"UNRHXEPDKXPRTM-UHFFFAOYSA-N","LD50":[{"dosages":[{"amount":"665 mg/kg","route":"oral"},{"amount":"300 mg/kg","route":"intraperitoneal"}],"organism":"Mouse"}],"MeSH Pharmacological Classification":"Agents that control agitated psychotic behavior, alleviate acute psychotic states, reduce psychotic symptoms, and exert a quieting effect. They are used in SCHIZOPHRENIA; senile dementia; transient psychosis following surgery; or MYOCARDIAL INFARCTION; etc. These drugs are often referred to as neuroleptics alluding to the tendency to produce neurological side effects, but not all antipsychotics are likely to produce such effects. Many of these drugs may also be effective against nausea, emesis, and pruritus.","MolecularFormula":"C\u003csub\u003e17\u003c/sub\u003eH\u003csub\u003e26\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e4\u003c/sub\u003eS","MolecularWeight":"354.5 g/mol","Opticalactivity":"( + / - )","PubChemId":5357,"RefCount":4,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Sultopride","Name":"Sultopride","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q4445779","Name":"Sultopride","Sub":false}]},{"Name":"DrugBank","Urls":[{"Link":"https://go.drugbank.com/drugs/DB13273","Name":"Sultopride","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/5357","Name":"Sultopride","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL277945","Name":"Sultopride","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:9356","Name":"Sultopride","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=53583-79-2","Name":"Sultopride","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0258623","Name":"Sultopride","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C11708","Name":"Sultopride","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/AA0G3TW31W","Name":"Sultopride","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID9023627","Name":"Sultopride","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 5357, Sultopride. Accessed October 2, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/5357\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/5357\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Sultopride. UNII: AA0G3TW31W. Global Substance Registration System. Accessed October 2, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/AA0G3TW31W\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/AA0G3TW31W\u003c/a\u003e","Anvisa. RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. March 31, 2023. Accessed October 2, 2025. \u003ca href=https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003ehttps://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-784-de-31-de-marco-de-2023-474904992\u003c/a\u003e"],"SMILES":"CCN1CCCC1CNC(=O)C2=C(C=CC(=C2)S(=O)(=O)CC)OC","SaltData":[{"AcidCount":1,"Amine":"Sultopride","AmineCount":1,"Formula":"Cl","Name":"hydrochloride","Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 128.385 93.405\"\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=\"#ff0d0d\" stroke=\"#000\" stroke-linecap=\"round\" stroke-linejoin=\"round\" stroke-width=\".7\"\u003e\u003cpath fill=\"#fff\" stroke=\"none\" d=\"M0 0h129v94H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m73.773 71.843-3.197-14.901M70.576 56.942l8.326-7.526M85.192 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