U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C18H19NO4
Molecular Weight 313.3478
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of N-TRANS-FERULOYLTRAMINE

SMILES

COC1=C(O)C=CC(\C=C\C(=O)NCCC2=CC=C(O)C=C2)=C1

InChI

InChIKey=NPNNKDMSXVRADT-WEVVVXLNSA-N
InChI=1S/C18H19NO4/c1-23-17-12-14(4-8-16(17)21)5-9-18(22)19-11-10-13-2-6-15(20)7-3-13/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)/b9-5+

HIDE SMILES / InChI

Molecular Formula C18H19NO4
Molecular Weight 313.3478
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
[Studies on the chemical constituents of Annona squamosa].
1992
Antioxidant and lipophilic constituents of Tinospora crispa.
1998 Jun
Nature is the best source of anti-inflammatory drugs: indexing natural products for their anti-inflammatory bioactivity.
2018 Jan
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:52:45 GMT 2023
Edited
by admin
on Sat Dec 16 08:52:45 GMT 2023
Record UNII
WC99S6JM5Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-TRANS-FERULOYLTRAMINE
Common Name English
N-E-FERULOYL TYRAMINE
Common Name English
N-FERYROYLTYRAMINE
Common Name English
MOUPINAMIDE
Common Name English
2-PROPENAMIDE, 3-(4-HYDROXY-3-METHOXYPHENYL)-N-(2-(4-HYDROXYPHENYL)ETHYL)-, (2E)-
Systematic Name English
N-P-TRANS-HYDROXYPHENETHYL FERULAMINE
Common Name English
FERULOYL TYRAMINE
Common Name English
(E)-N-FERULOYLTYRAMINE
Common Name English
2-PROPENAMIDE, 3-(4-HYDROXY-3-METHOXYPHENYL)-N-(2-(4-HYDROXYPHENYL)ETHYL)-
Systematic Name English
ALFRUTAMIDE
Common Name English
(E)-3-(4-HYDROXY-3-METHOXYPHENYL)-N-(4-HYDROXYPHENETHYL)ACRYLAMIDE
Systematic Name English
Code System Code Type Description
PUBCHEM
5280537
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
PRIMARY
FDA UNII
WC99S6JM5Y
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID30904143
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
PRIMARY
CHEBI
17818
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
PRIMARY
CAS
66648-43-9
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
PRIMARY
CAS
65646-26-6
Created by admin on Sat Dec 16 08:52:45 GMT 2023 , Edited by admin on Sat Dec 16 08:52:45 GMT 2023
NON-SPECIFIC STEREOCHEMISTRY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
A 70% aq. acetone extract prepared from the leaves of N. tabacum was partitioned between EtOAc and H2O. TMV infection inhibition activity of compound 18.2 ? 2.5%.
PARENT -> CONSTITUENT ALWAYS PRESENT
270 uM IC50 vs in vitro prostaglandin synthesis
PARENT -> CONSTITUENT ALWAYS PRESENT
Amide