Trp | |
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Esters [] | |
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Tryptophan benzoate | |
Molecular structure via molpic based on CDK |
Physical properties [] | |
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Molecular mass | 204.22 g/mol [1] |
Melting point | 293 °C [1] |
Boiling point | 289.00 to 291.00 °C. @ 760.00 mm Hg [1] |
Predicted LogP | -1.1 [1] |
Structural Identifiers [] | |
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Molecular formula | C11H12N2O2 [1] |
IUPAC name | 2-amino-3-(1H-indol-3-yl)propanoic acid [1] |
SMILES | C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N [1] |
InChI | InChI=1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15) [1] |
InChIKey | QIVBCDIJIAJPQS-UHFFFAOYSA-N [1] |
Tryptophan
Tryptophan (also known as -Tryptophan, Tryptophan, dl-, CCRIS 719, AI3-24395, DLTrytophane, DL3βIndolylalanine, DLαAmino3indolepropionic acid, 200-194-9, Trytophan or Racemic Tryptophan) is a
Chemistry
Esters []
Tryptophan is typically found in the form of its ester.
Stereochemistry []
(RS)-Tryptophan is a racemic mixture of the optical stereoisomers
Anodyne Usernotes [] | |
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0xea / Tryptophan via | Uncertain Activity |
Experience reports []
There are currently 2 experience reports involving tryptophan on OpenErowid:
See also []
External links []
- Tryptophan (Wikipedia)
- Tryptophan / (+)-Tryptophan (Wikidata)
- Tryptophan / (+)-Tryptophan (PubChem)
- Tryptophan / (+)-Tryptophan (ChEMBL)
- Tryptophan / (+)-Tryptophan (ChEBI)
- Tryptophan / (+)-Tryptophan (Common Chemistry)
- Tryptophan / (+)-Tryptophan (HMDB)
- Tryptophan / (+)-Tryptophan (KEGG)
- Tryptophan / (+)-Tryptophan (UNII)
- Tryptophan / (+)-Tryptophan (EPA DSSTox)
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 1148, Tryptophan. Accessed June 28, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/1148
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Tryptophan. UNII: X9U7434L7A. Global Substance Registration System. Accessed June 28, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/X9U7434L7A