{"Abbreviation":["GVS-111"],"Aliases":["Noopept","GVS-111","J759.455K","omberacetamum","RefChem:854682","1-(2-Phenylacetyl)-L-prolylglycine ethy ester","Ethyl 2-(1-(2-phenylacetyl)pyrrolidine-2-carboxamido)acetate","n-phenylacetyl-l-prolylglycine ethyl ester","Glycine, 1-(phenylacetyl)-L-prolyl-, ethyl ester","N-(1-(Phenylacetyl)-L-prolyl)glycine ethyl ester","Glycine, 1-(2-phenylacetyl)-L-prolyl-, ethyl ester","ethyl (2-phenylacetyl)-L-prolylglycinate","1-(2-phenylacetyl)-l-prolylglycine ethyl ester","GVS 111","N-[1-(Phenylacetyl)-L-prolyl]glycine Ethyl Ester","N-Phenylacetyl-L-prolylglycine ethyl ester;SGS 111","ethyl phenylacetyl-Pro-Gly","SGS-111","ethyl 2-{[(2S)-1-(2-phenylacetyl)pyrrolidin-2-yl]formamido}acetate","Glycine, N-(1-(phenylacetyl)-L-prolyl)-, ethyl ester","ethyl 1-(phenylacetyl)-L-prolylglycinate","Noopept - Bio-X trade mark","Noopept, \u003e=98%","CTK4C9275","DVD-111"],"CAS":"157115-85-0","ChEMBL":"CHEMBL4303687","ChemicalClasses":["carboxylic acid"],"Chirality":"absolute","Esters":[],"European Community (EC) Number":"839-170-3","Formating":[],"HeavyAtomCount":23,"IUPACName":"ethyl 2-[[(2S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyl]amino]acetate","InChI":"InChI=1S/C17H22N2O4/c1-2-23-16(21)12-18-17(22)14-9-6-10-19(14)15(20)11-13-7-4-3-5-8-13/h3-5,7-8,14H,2,6,9-12H2,1H3,(H,18,22)/t14-/m0/s1","InChIKey":"PJNSMUBMSNAEEN-AWEZNQCLSA-N","MeSH Pharmacological Classification":"Drugs intended to prevent damage to the brain or spinal cord from ischemia, stroke, convulsions, or trauma. Some must be administered before the event, but others may be effective for some time after. They act by a variety of mechanisms, but often directly or indirectly minimize the damage produced by endogenous excitatory amino acids.","MolecularFormula":"C\u003csub\u003e17\u003c/sub\u003eH\u003csub\u003e22\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO\u003csub\u003e4\u003c/sub\u003e","MolecularWeight":"318.4 g/mol","Opticalactivity":"UNSPECIFIED","PubChemId":180496,"RefCount":3,"RefCur":"","References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Omberacetam","Name":"Omberacetam","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q7049784","Name":"Omberacetam","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/180496","Name":"Omberacetam","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL4303687","Name":"Omberacetam","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=157115-85-0","Name":"Omberacetam","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/4QBJ98683M","Name":"Omberacetam","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID80166214","Name":"Omberacetam","Sub":false}]}],"Refs":["National Center for Biotechnology Information. PubChem Compound Summary for CID 180496, Omberacetam. Accessed October 2, 2025. \u003ca href=https://pubchem.ncbi.nlm.nih.gov/compound/180496\u003ehttps://pubchem.ncbi.nlm.nih.gov/compound/180496\u003c/a\u003e","U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Omberacetam. UNII: 4QBJ98683M. Global Substance Registration System. Accessed October 2, 2025. \u003ca href=https://gsrs.ncats.nih.gov/ginas/app/beta/substances/4QBJ98683M\u003ehttps://gsrs.ncats.nih.gov/ginas/app/beta/substances/4QBJ98683M\u003c/a\u003e"],"SMILES":"CCOC(=O)CNC(=O)[C@@H]1CCCN1C(=O)CC2=CC=CC=C2","SaltData":[],"Salts":[],"Scheduling":[{"gov":"Australia","ref":[],"schedule":"S4 substance"},{"gov":"United States","ref":[],"schedule":"Unapproved \"New Drug\" (as defined by 21 U.S. Code § 321(p)(1)). Use in dietary supplements, food, or medicine is unlawful; otherwise uncontrolled."}],"StereoisomerData":[],"Stereoisomers":[],"Structure":"\u003csvg xmlns=\"http://www.w3.org/2000/svg\" preserveAspectRatio=\"none\" style=\"display:block\" viewBox=\"0 0 118.332 97.16\"\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 0h119v98H0z\"/\u003e\u003cg class=\"mol\"\u003e\u003cpath d=\"m1.038 96.122 13.198-7.62M14.236 88.502V77.183M17.515 71.369l9.92-5.727\" class=\"bond\"/\u003e\u003cg class=\"bond\"\u003e\u003cpath d=\"M26.215 66.345V54.323M28.654 66.345V54.323\"/\u003e\u003cpath stroke=\"#ff0d0d\" d=\"M26.215 54.323v6.011M28.654 54.323v6.011\" class=\"hi\"/\u003e\u003c/g\u003e\u003cpath d=\"m27.435 65.642 13.198 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