Type : Indole, Derivative of Tryptophan
Chemical_Nomenclature : (S)-N-(2-(1H-indol-3-yl)ethyl)-2-((3-fluoro-4-hydroxybenzyl)amino)-3-(1H-indol-3-yl)-N-methylpropanamide
Canonical SMILES : C1(=C[N]C2=CC=CC=C12)C[C@H](C(N(CCC3=C[N]C4=C3C=CC=C4)C)=O)NCC5=CC(=C(C=C5)O)F
InChI : InChI=1S\/C29H29FN4O2\/c1-34(13-12-20-17-32-25-8-4-2-6-22(20)25)29(36)27(31-16-19-10-11-28(35)24(30)14-19)15-21-18-33-26-9-5-3-7-23(21)26\/h2-11,14,17-18,27,31-33,35H,12-13,15-16H2,1H3\/t27-\/m1\/s1
InChIKey : JPVRSCPFKPOFIM-HHHXNRCGSA-N
Other name(s) : Compound 4d-13
| Title : Design, synthesis and evaluation of novel L-tryptophan derivatives as multifunctional agents with cholinesterase inhibition, anti-beta-amyloid aggregation, anti-inflammatory, antioxidant and neuroprotection properties against Alzheimer's disease - Yu_2025_Bioorg.Chem_161_108478 |
| Author(s) : Yu H , Chen Y , Li H , Li Z , Cui Y , Han S , Zeng X , Cheng S , Feng Y |
| Ref : Bioorg Chem , 161 :108478 , 2025 |
| Abstract : |
| PubMedSearch : Yu_2025_Bioorg.Chem_161_108478 |
| PubMedID: 40318509 |