{"id":24780,"npaid":"NPA024780","original_name":"Muscimol","mol_formula":"C4H6N2O2","mol_weight":"114.1040","exact_mass":"114.0429","inchikey":"ZJQHPWUVQPJPQT-UHFFFAOYSA-N","smiles":"C1=C(ONC1=O)CN","cluster_id":7555,"node_id":5169,"has_exclusions":false,"synonyms":[],"inchi":"InChI=1S/C4H6N2O2/c5-2-3-1-4(7)6-8-3/h1H,2,5H2,(H,6,7)","m_plus_h":"115.0502","m_plus_na":"137.0321","origin_reference":{"doi":"10.5281/zenodo.3766313","pmid":5629522,"authors":"Eugster CH","title":"Isolation, structure, and syntheses of central-active compounds from Amanita muscaria (L. ex Fr.) hooker.","journal":"Psychopharmacology Bulletin","year":1967,"volume":"4","issue":"3","pages":"18-19"},"origin_organism":{"id":8707,"type":"Fungus","genus":"Amanita","species":"muscaria","taxon":{"id":1391,"name":"Amanita","rank":"genus","taxon_db":"mycobank","external_id":"17045","ncbi_id":41955,"ancestors":[{"id":599,"name":"Eukarya","rank":"domain","taxon_db":"mycobank","external_id":"0","ncbi_id":2759},{"id":600,"name":"Fungi","rank":"kingdom","taxon_db":"mycobank","external_id":"90157","ncbi_id":4751},{"id":1365,"name":"Basidiomycota","rank":"phylum","taxon_db":"mycobank","external_id":"90050","ncbi_id":5204},{"id":1366,"name":"Agaricomycetes","rank":"class","taxon_db":"mycobank","external_id":"501297","ncbi_id":155619},{"id":1367,"name":"Agaricales","rank":"order","taxon_db":"mycobank","external_id":"90508","ncbi_id":5338},{"id":1390,"name":"Amanitaceae","rank":"family","taxon_db":"mycobank","external_id":"817322","ncbi_id":41954}]}},"syntheses":[],"reassignments":[],"mol_structures":[{"current_structure":true,"reference_doi":"10.5281/zenodo.3766313","structure_smiles":"C1=C(ONC1=O)CN","is_reassignment":false,"version":1}],"exclusions":[],"external_ids":[{"external_db_name":"gnps","external_db_code":"CCMSLIB00000219584%Massbank:KO003527 Muscimol%3!CCMSLIB00000219587%Massbank:KO003528 Muscimol%3!CCMSLIB00000219589%Massbank:KO003529 Muscimol%3!CCMSLIB00000219591%Massbank:KO003530 Muscimol%3!CCMSLIB00000219592%Massbank:KO003531 Muscimol%3"},{"external_db_name":"npmrd","external_db_code":"NP0021691"},{"external_db_name":"cmmc","external_db_code":"https://cmmc-kb.gnps2.org/structurepage/?inchikey=ZJQHPWUVQPJPQT-UHFFFAOYSA-N"}],"classyfire":{"class":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000278","name":"Organonitrogen compounds","chemont_id":"CHEMONTID:0000278","description":"Organic compounds containing a nitrogen atom."},"smiles":"NCC1=CC(=O)NO1","kingdom":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0000000","name":"Organic compounds","chemont_id":"CHEMONTID:0000000","description":"Compounds that contain at least one carbon atom, excluding isocyanide/cyanide and their non-hydrocarbyl derivatives, thiophosgene, carbon diselenide, carbon monosulfide, carbon disulfide, carbon subsulfide, carbon monoxide, carbon dioxide, Carbon suboxide, and dicarbon monoxide."},"inchikey":"InChIKey=ZJQHPWUVQPJPQT-UHFFFAOYSA-N","subclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0002449","name":"Amines","chemont_id":"CHEMONTID:0002449","description":"Compounds formally derived from ammonia by replacing one, two or three hydrogen atoms by hydrocarbyl groups, and having the general structures RNH2 (primary amines), R2NH (secondary amines), R3N (tertiary amines)."},"ancestors":["Amines","Aralkylamines","Azacyclic compounds","Azoles","Chemical entities","Heteroaromatic compounds","Hydrocarbon derivatives","Isoxazoles","Lactams","Monoalkylamines","Organic compounds","Organic nitrogen compounds","Organic oxides","Organic oxygen compounds","Organoheterocyclic compounds","Organonitrogen compounds","Organooxygen compounds","Organopnictogen compounds","Oxacyclic compounds","Primary amines"],"superclass":{"url":"http://classyfire.wishartlab.com/tax_nodes/C0004707","name":"Organic nitrogen compounds","chemont_id":"CHEMONTID:0004707","description":"Organic compounds containing a nitrogen atom."},"description":"This compound belongs to the class of organic compounds known as aralkylamines. 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