{"Abbreviation":"OCT","Aliases":["(R)-octopamine","D-Octopamine","(R)-p-Octopamine","D-(-)-Octopamine","Octopamine, (-)-","p-Octopamine","dl-Octopamine","Benzenemethanol, α-(aminomethyl)-4-hydroxy-, (αR)-","4-(2R-amino-1-hydroxyethyl)phenol","2-Amino-1-(4-hydroxyphenyl)ethanol"],"CAS":"876-04-0","ChEBI":"CHEBI:44715","ChEMBL":"CHEMBL1160703","ChemicalClasses":["phenylethanolamine"],"Chirality":"absolute","Classes":["Neurotransmitters"],"Dosing Info":[],"DrugClasses":[],"HMDB ID":"HMDB0004825","HeavyAtomCount":11,"IUPACName":"4-[(1R)-2-amino-1-hydroxyethyl]phenol","InChI":"InChI=1S/C8H11NO2/c9-5-8(11)6-1-3-7(10)4-2-6/h1-4,8,10-11H,5,9H2/t8-/m0/s1","InChIKey":"QHGUCRYDKWKLMG-QMMMGPOBSA-N","MeSH Pharmacological Classification":"Drugs that selectively bind to and activate alpha adrenergic receptors. (See all compounds classified as Adrenergic alpha-Agonists.)","MolecularFormula":"C\u003csub\u003e8\u003c/sub\u003eH\u003csub\u003e11\u003c/sub\u003eNO\u003csub\u003e2\u003c/sub\u003e","MolecularWeight":"153.18 g/mol","Opticalactivity":"UNSPECIFIED","Physical Description":"Solid","PrevSalts":[],"PubChemId":440266,"Record Description":["(R)-octopamine is an octopamine. It is an enantiomer of a (S)-octopamine.","p-Hydroxyphenylethanolamine has been reported in Aplysia californica, Fascaplysinopsis reticulata, and other organisms with data available.","An alpha-adrenergic sympathomimetic amine, biosynthesized from tyramine in the CNS and platelets and also in invertebrate nervous systems. It is used to treat hypotension and as a cardiotonic. The natural D(-) form is more potent than the L(+) form in producing cardiovascular adrenergic responses. It is also a neurotransmitter in some invertebrates.","See also: Octopamine (annotation moved to).","(R)-octopamine is an octopamine. It is an enantiomer of a (S)-octopamine."],"References":[{"Name":"Wikipedia","Urls":[{"Link":"https://en.wikipedia.org/wiki/Octopamine","Name":"Octopamine","Sub":false}]},{"Name":"Wikidata","Urls":[{"Link":"https://www.wikidata.org/wiki/Q27104536","Name":"Octopamine","Sub":false}]},{"Name":"PubChem","Urls":[{"Link":"https://pubchem.ncbi.nlm.nih.gov/compound/440266","Name":"Octopamine","Sub":false}]},{"Name":"ChEMBL","Urls":[{"Link":"https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1160703","Name":"Octopamine","Sub":false}]},{"Name":"ChEBI","Urls":[{"Link":"https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:44715","Name":"Octopamine","Sub":false}]},{"Name":"Common Chemistry","Urls":[{"Link":"https://commonchemistry.cas.org/detail?cas_rn=876-04-0","Name":"Octopamine","Sub":false}]},{"Name":"HMDB","Urls":[{"Link":"https://hmdb.ca/metabolites/HMDB0004825","Name":"Octopamine","Sub":false}]},{"Name":"KEGG","Urls":[{"Link":"https://www.kegg.jp/entry/C04227","Name":"Octopamine","Sub":false}]},{"Name":"UNII","Urls":[{"Link":"https://gsrs.ncats.nih.gov/ginas/app/ui/substances/H1P36W1J84","Name":"Octopamine","Sub":false}]},{"Name":"EPA DSSTox","Urls":[{"Link":"https://comptox.epa.gov/dashboard/chemical/details/DTXSID901317465","Name":"Octopamine","Sub":false}]}],"SMILES":"C1=CC(=CC=C1[C@H](CN)O)O","StoreUNII":["H1P36W1J84"],"StructureBase64":"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