{"Abbreviation":"4-HO-T","Aliases":["3-(2-aminoethyl)-indol-4-ol","836-014-6","Pdsp1_000531","Pdsp2_000529","3-(2-Amino-ethyl)-1H-indol-4-ol","3-(2-Amino-ethyl)-1H-indol-4-ol(4-HT)","C21762","En300-372905"],"CAS":"570-14-9","ChEBI":"CHEBI:139217","ChEMBL":"CHEMBL18855","ChemicalClasses":["tryptamine"],"Chirality":"achiral","Classes":null,"Dosing Info":[],"DrugClasses":[],"DurationOfAction":"","EliminationHalfLife":"","European Community (EC) Number":"836-014-6","HeavyAtomCount":13,"IUPACName":"3-(2-aminoethyl)-1H-indol-4-ol","InChI":"InChI=1S/C10H12N2O/c11-5-4-7-6-12-8-2-1-3-9(13)10(7)8/h1-3,6,12-13H,4-5,11H2","InChIKey":"FKIRTWDHOWAQGX-UHFFFAOYSA-N","MolecularFormula":"C\u003csub\u003e10\u003c/sub\u003eH\u003csub\u003e12\u003c/sub\u003eN\u003csub\u003e2\u003c/sub\u003eO","MolecularWeight":"176.21 g/mol","PD":"PD094269","PrevSalts":[],"PubChemId":11297,"Record Description":["4-hydroxytryptamine is a member of the class of tryptamines that is tryptamine in which the the indole ring has been substituted by a hydroxy group at position 4. It is a member of tryptamines, a member of hydroxyindoles and a primary amino compound. It is a conjugate base of a 4-hydroxytryptamine(1+).","4-hydroxytryptamine is a member of the class of tryptamines that is tryptamine in which the the indole ring has been substituted by a hydroxy group at position 4. It is a member of tryptamines, a member of hydroxyindoles and a primary amino compound. It is a conjugate base of a 4-hydroxytryptamine(1+)."],"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/4-Hydroxytryptamine","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q27276515","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/11297","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL18855","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:139217","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"Probes \u0026 Drugs","Urls":[{"Link":"https://www.probes-drugs.org/compound/PD094269","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=570-14-9","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C21762","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/DP0D1701D1","Name":"4-Hydroxytryptamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID30205607","Name":"4-Hydroxytryptamine","Sub":false}]}],"SMILES":"C1=CC2=C(C(=C1)O)C(=CN2)CCN","Scheduling":[],"StoreUNII":["DP0D1701D1"],"StructureBase64":"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