19255 <common-name>Aniracetam</common-name> <description>Aniracetam is an organic compound with the chemical formula C12H13NO3 and an average molecular weight of 219.24 g/mol. Aniracetam belongs to the benzoic acids and derivatives, a subclass of benzene and substituted derivatives within the organic compounds. It is categorized within the superclass of benzenoids. The compound has been identified in three recorded sources. These include electrically stimulated smoking devices found in electrical and electronic equipment, as well as household cleaning and consumer products such as tobacco smoke filters, cigarettes, and cigars. In terms of biological activity, aniracetam is associated with four recorded protein targets. It acts as an inhibitor of the D(2) dopamine receptor (DRD2) and the 5-hydroxytryptamine receptor 2A (HTR2A). Additionally, it targets glutamate receptor 2 (GRIA2) and glutamate receptor 3 (GRIA3).</description> <cas>72432-10-1</cas> <pubchem-id>2196</pubchem-id> <chemical-formula>C12H13NO3</chemical-formula> <weight>219.24</weight> <appearance nil="true"/> <melting-point nil="true"/> <boiling-point nil="true"/> <density nil="true"/> <solubility nil="true"/> <specific-gravity nil="true"/> <flash-point nil="true"/> <vapour-pressure nil="true"/> <route-of-exposure nil="true"/> <target nil="true"/> <mechanism-of-toxicity nil="true"/> <metabolism nil="true"/> <toxicity nil="true"/> <lethaldose nil="true"/> <carcinogenicity nil="true"/> <use-source nil="true"/> <min-risk-level nil="true"/> <health-effects nil="true"/> <symptoms nil="true"/> <treatment nil="true"/> <created-at type="dateTime">2016-05-22T05:01:56Z</created-at> <updated-at type="dateTime">2026-08-18T17:20:01Z</updated-at> <interacting-proteins nil="true"/> <wikipedia nil="true"/> <uniprot-id nil="true"/> <kegg-compound-id nil="true"/> <omim-id nil="true"/> <chebi-id nil="true"/> <biocyc-id nil="true"/> <ctd-id nil="true"/> <stitch-id nil="true"/> <drugbank-id>DB04599</drugbank-id> <pdb-id nil="true"/> <actor-id nil="true"/> <organism nil="true"/> <export type="boolean">true</export> <metabolizing-proteins nil="true"/> <transporting-proteins nil="true"/> <moldb-smiles>COC1=CC=C(C=C1)C(=O)N1CCCC1=O</moldb-smiles> <moldb-formula>C12H13NO3</moldb-formula> <moldb-inchi>InChI=1S/C12H13NO3/c1-16-10-6-4-9(5-7-10)12(15)13-8-2-3-11(13)14/h4-7H,2-3,8H2,1H3</moldb-inchi> <moldb-inchikey>ZXNRTKGTQJPIJK-UHFFFAOYSA-N</moldb-inchikey> <moldb-average-mass type="decimal">219.2365</moldb-average-mass> <moldb-mono-mass type="decimal">219.089543287</moldb-mono-mass> <origin nil="true"/> <state nil="true"/> <logp>1.11</logp> <hmdb-id nil="true"/> <chembl-id nil="true"/> <chemspider-id>2111</chemspider-id> <structure-image-file-name nil="true"/> <structure-image-content-type nil="true"/> <structure-image-file-size type="integer" nil="true"/> <structure-image-updated-at type="dateTime" nil="true"/> <biodb-id nil="true"/> <synthesis-reference nil="true"/> <structure-image-caption nil="true"/> <chemdb-id>CHEM018150</chemdb-id> <dsstox-id>DTXSID5045128</dsstox-id> <toxcast-id>45128</toxcast-id> <stoff-ident-origin nil="true"/> <stoff-ident-id nil="true"/> <susdat-id>NS00017748</susdat-id> <iupac>1-(4-methoxybenzoyl)pyrrolidin-2-one</iupac> <moldb-polar-surface-area>46.61000000000001</moldb-polar-surface-area> <moldb-refractivity>58.9575</moldb-refractivity> <moldb-polarizability>22.59987974107648</moldb-polarizability> <moldb-rotatable-bond-count>2</moldb-rotatable-bond-count> <moldb-acceptor-count>3</moldb-acceptor-count> <moldb-donor-count>0</moldb-donor-count> <moldb-pka-strongest-acidic nil="true"/> <moldb-pka-strongest-basic>-4.791258059303984</moldb-pka-strongest-basic> <moldb-physiological-charge>0</moldb-physiological-charge> <moldb-number-of-rings>2</moldb-number-of-rings> <moldb-alogps-logp>0.55</moldb-alogps-logp> <moldb-alogps-logs>-1.95</moldb-alogps-logs> <moldb-alogps-solubility>2.47e+00 g/l</moldb-alogps-solubility> <kingdom>Organic compounds</kingdom> <superklass>Benzenoids</superklass> <klass>Benzene and substituted derivatives</klass> <subklass>Benzoic acids and derivatives</subklass> <paper-count type="integer">615</paper-count> <sync-id>CED0010308</sync-id> <structure-inchikey>ZXNRTKGTQJPIJK-UHFFFAOYSA-N</structure-inchikey> <structure-fingerprint>20200000000000000000000000000000000010000000000000000000000000000000000000000000000020000000000100000200000000000000040002010000010040000000000000000000020100000000000000000000000800000040000000000000000000200000000002000000010000000000000000000000000000000000000000085008000000000000000000008000008100000090000000000000000000000000000000000000004000000000200200000000000000000000000000000040000000000400000000000000000000000000000000</structure-fingerprint> <structure-pattern-fingerprint>400000000122060080000000010820000000040001052000003400400200000c40060050008000000000410800800000042000a1808c30010200443000a04000c4110400021006000090100000620200000001805001113240000422000009000c200406004082002000000054100001200080100121c0043118022002110002004000180c40020808000200080c0008111c0012444016820000080000400084004300001000c00000000940053c211002c00000894108401801020008400a100010000404000012018000040401028000000000020050200d0000040800000000000812000100000000000240022000001000108640000a0000008050000006</structure-pattern-fingerprint> <structure-pickle>ï¾­Þ������������������������€���`�������(������@(������@h�������@h�������@(������@h�������@h��������(�������(�������(�������`�������`�������`�������(�������(����������� ��h���h���h���h���h��� � (�� ������ � ����(���h�� B������������� � �����������</structure-pickle> <structure-indexed-at type="dateTime">2026-09-19T04:07:32Z</structure-indexed-at> </compound>