N-trans-feruloyl-3-methoxytyramine
AlkaPlorer ID: AK021929
Synonym: '', '(2E)-3-(4-Hydroxy-3-methoxyphenyl)-N-2-(4-hydroxy-3-methoxyphenyl)ethylacrylamide', 'trans-N-feruloyl-3-O-methyldopamine'
IUPAC Name: 3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]prop-2-enamide
Structure
SMILES: COC1=CC(C=CC(O)=NCCC2=CC=C(O)C(OC)=C2)=CC=C1O
InChI: InChI=1S/C19H21NO5/c1-24-17-11-13(3-6-15(17)21)5-8-19(23)20-10-9-14-4-7-16(22)18(12-14)25-2/h3-8,11-12,21-22H,9-10H2,1-2H3,(H,20,23)
InChIKey: GRXBVKANHNUZNL-UHFFFAOYSA-N
Reference
Secondary Metabolites from the Roots of <i>Litsea hypophaea</i> and Their Antitubercular Activity
PubChem CID: 134313
CAS: 78510-19-7
LOTUS: LTS0159666
COCONUT: CNP0198232
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Neolitsea konishii | Neolitsea | Lauraceae | Laurales | Magnoliopsida | Streptophyta | Viridiplantae | Eukaryota |
Properties Information
Molecule Weight: 343.379
TPSA？: 91.51
MolLogP？: 3.327400000000002
Number of H-Donors: 3
Number of H-Acceptors: 5
RingCount: 2
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|