| Weight | 204.229 g/mol |
|---|---|
| Formula | C11H12N2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
D-Tryptophan (153-94-6)
Score:
#1372 in Biochemistry
,
#3312 in Biology
,
#4132 in Chemistry
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- Novel tryptophan catabolic enzyme IDO2 is the preferred biochemical target of the antitumor indoleamine 2,3-dioxygenase inhibitory compound D-1-methyl-tryptophan. (Cancer Research, 2007)
- Synthesis of gold nanoplates by aspartate reduction of gold chlorideElectronic supplementary information (ESI) available: Fig. S1. UV/Visible-NIR extinction spectra of an aqueous dispersion of gold nanoparticles synthesized by tyrosine (a), phenylalanine (b), lysine (c), aspartate (d) and tryptophan (e). See http://www.rsc.org/suppdata/cc/b3/b315732f/ (Chemical Communications, 2004)
- Tryptophan Pyrrolase of Rabbit Intestine d- AND l-TRYPTOPHAN-CLEAVING ENZYME OR ENZYMES (Journal of Biological Chemistry, 1967)
- IDO inhibits a tryptophan sufficiency signal that stimulates mTOR: A novel IDO effector pathway targeted by D-1-methyl-tryptophan. (OncoImmunology, 2012)
- Contryphan Is a D-Tryptophan-containing Conus Peptide (Journal of Biological Chemistry, 1996)
- Characterization of the binding and chiral separation of d- and l-tryptophan on a high-performance immobilized human serum albumin column (Journal of Chromatography A, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N
-
InChIKeyQIVBCDIJIAJPQS-UHFFFAOYSA-N
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