| Weight | 203.245 g/mol |
|---|---|
| Formula | C11H13N3O |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
L-Tryptophanamide (20696-57-5)
tryptophanamide · tryptophanamide, (+-)-isomer · tryptophanamide monohydrochloride, (S)-isomer
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- Investigations of the Chymotrypsin-catalyzed Hydrolysis of Specific Substrates I. THE pH DEPENDENCE OF THE CATALYTIC HYDROLYSIS OF N-ACETYL-l-TRYPTOPHANAMIDE BY THREE FORMS OF THE ENZYME AT ALKALINE pH (Journal of Biological Chemistry, 1967)
- Anisotropy spectra of indole and N-acetyl-L-tryptophanamide observed for two-photon excitation of fluorescence (Chemical Physics Letters, 1992)
- The fluorescence and circular dichroism of proteins in reverse micelles: application to the photophysics of human serum albumin and N-acetyl-L-tryptophanamide (Biophysical Chemistry, 1996)
- Unassisted Transport of N-acetyl-L-tryptophanamide through Membrane: Experiment and Simulation of Kinetics (Journal of Physical Chemistry B, 2012)
- PHOTOKINETIC AND PHOTOPHYSICAL MEASUREMENTS OF THE SENSITIZED PHOTOOXIDATION OF THE TRYPTOPHYL RESIDUE IN NACETYL TRYPTOPHANAMIDE AND IN HUMAN SERUM ALBUMIN (Photochemistry and Photobiology, 1987)
- FLASH PHOTOLYSIS OF TRYPTOPHAN AND NACETYLLTRYPTOPHANAMIDE; THE EFFECT OF BROMIDE ON TRANSIENT YIELDS (Photochemistry and Photobiology, 1977)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - tryptophanamide
- tryptophanamide, (+-)-isomer
- tryptophanamide monohydrochloride, (S)-isomer
- tryptophanamide, (S)-isomer
-
SMILESC1=CC=C2C(=C1)C(=CN2)CC(C(=O)N)N
-
InChIKeyJLSKPBDKNIXMBS-UHFFFAOYSA-N
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