N-acetylserotonin
General
Type : Derivative of Tryptamine || Indole || Not A\/B H target || Natural
Chemical_Nomenclature : N-[2-(5-hydroxy-1H-indol-3-yl)ethyl]acetamide
Canonical SMILES : CC(=O)NCCC1=CNC2=C1C=C(C=C2)O
InChI : InChI=1S\/C12H14N2O2\/c1-8(15)13-5-4-9-7-14-12-3-2-10(16)6-11(9)12\/h2-3,6-7,14,16H,4-5H2,1H3,(H,13,15)
InChIKey : MVAWJSIDNICKHF-UHFFFAOYSA-N
Other name(s) : N-Acetyl-5-hydroxytryptamine, N-[2-(5-Hydroxy-1H-indol-3-yl)ethyl]acetamide, Normelatonin, CHEMBL33103, CHEBI:17697, ZINC66104, DB04275, N-acetylserotonine, Desmethylmelatonin
Target
Families : Arylacetamide_deacetylase
References (1)
| Title : In vitro deacetylation of N-acetylserotonin by arylacetamide deacetylase - Huang_2023_J.Pineal.Res_75_e12870 |
| Author(s) : Huang Z , Li Y , Konishi K , Sakai Y , Tashiro K , Fukami T , Borjigin J |
| Ref : J Pineal Res , 75 :e12870 , 2023 |
| Abstract : Huang_2023_J.Pineal.Res_75_e12870 |
| ESTHER : Huang_2023_J.Pineal.Res_75_e12870 |
| PubMedSearch : Huang_2023_J.Pineal.Res_75_e12870 |
| PubMedID: 37002641 |