Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H18N2O3 |
| Molecular Weight | 274.315 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)[C@H](CC1=CNC2=C1C=CC=C2)NC(C)=O
InChI
InChIKey=KQGQONPKSKUHHT-AWEZNQCLSA-N
InChI=1S/C15H18N2O3/c1-3-20-15(19)14(17-10(2)18)8-11-9-16-13-7-5-4-6-12(11)13/h4-7,9,14,16H,3,8H2,1-2H3,(H,17,18)/t14-/m0/s1
| Molecular Formula | C15H18N2O3 |
| Molecular Weight | 274.315 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Hydrogen bonding and solvent polarity markers in the uv resonance raman spectrum of tryptophan: application to membrane proteins. | 2009-11-05 |
|
| Solvent effects on the fluorescence quenching of tryptophan by amides via electron transfer. Experimental and computational studies. | 2009-03-05 |
|
| Methanolysis of ethyl esters of N-acetyl amino acids catalyzed by cyclosophoraoses isolated from Rhizobium meliloti. | 2008-02-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:51:31 GMT 2025
by
admin
on
Mon Mar 31 18:51:31 GMT 2025
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| Record UNII |
3779MVZ8JX
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| Record Status |
Validated (UNII)
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| Record Version |
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2382-80-1
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