DL-tryptophan

Summary

DL-tryptophan is a group of isomeric entities^[1].

Key Facts

• DL-tryptophan's instance of is recorded as group of isomeric entities^[2].
• DL-tryptophan's CAS Registry Number is recorded as 54-12-6^[3].
• DL-tryptophan's EC number is recorded as 200-194-9^[4].
• DL-tryptophan's canonical SMILES is recorded as C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N^[5].
• DL-tryptophan's InChI is recorded as 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)^[6].
• DL-tryptophan's InChIKey is recorded as QIVBCDIJIAJPQS-UHFFFAOYSA-N^[7].
• DL-tryptophan's chemical formula is recorded as C₁₁H₁₂N₂O₂^[8].
• DL-tryptophan's subclass of is recorded as aminoalkylindole^[9].
• DL-tryptophan's subclass of is recorded as aromatic amino acid^[10].
• DL-tryptophan's subclass of is recorded as tryptamine alkaloid^[11].
• DL-tryptophan's part of is recorded as tryptophan biosynthetic process^[12].
• DL-tryptophan's part of is recorded as tryptophan metabolic process^[13].
• DL-tryptophan's part of is recorded as tryptophan catabolic process^[14].
• DL-tryptophan's part of is recorded as serotonin biosynthetic process from tryptophan^[15].
• DL-tryptophan's part of is recorded as nicotinate nucleotide biosynthetic process from tryptophan^[16].
• DL-tryptophan's part of is recorded as tryptophan catabolic process to indole-3-acetate^[17].
• DL-tryptophan's part of is recorded as tryptophan catabolic process to kynurenine^[18].
• DL-tryptophan's part of is recorded as tryptophan catabolic process to acetyl-CoA^[19].
• DL-tryptophan's part of is recorded as tryptophan catabolic process to catechol^[20].
• DL-tryptophan's part of is recorded as tryptophan transport^[21].
• DL-tryptophan's ChEMBL ID is recorded as CHEMBL484901^[22].
• DL-tryptophan's UNII is recorded as X9U7434L7A^[23].
• DL-tryptophan's ChemSpider ID is recorded as 1116^[24].
• DL-tryptophan's PubChem CID is recorded as 1148^[25].
• DL-tryptophan's PubChem CID is recorded as 4099458^[26].