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CAS 6383-70-6

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5-(Phenylmethoxy)tryptophan

Description:
5-(Phenylmethoxy)tryptophan, with the CAS number 6383-70-6, is an amino acid derivative that features a tryptophan backbone modified with a phenylmethoxy group at the 5-position of the indole ring. This compound exhibits characteristics typical of tryptophan derivatives, including the ability to participate in hydrogen bonding due to the presence of the amino and carboxyl functional groups. The phenylmethoxy substituent enhances its lipophilicity, potentially influencing its solubility and interaction with biological membranes. As a tryptophan analog, it may play a role in biochemical pathways, particularly in the synthesis of neurotransmitters and other biologically active compounds. The compound is of interest in medicinal chemistry and pharmacology for its potential therapeutic applications, including effects on mood regulation and neuroprotection. Its structural features may also allow for interactions with various receptors and enzymes, making it a subject of study in drug design and development. Overall, 5-(Phenylmethoxy)tryptophan represents a unique chemical entity with potential implications in both research and therapeutic contexts.
Formula:C18H18N2O3
InChI:InChI=1S/C18H18N2O3/c19-16(18(21)22)8-13-10-20-17-7-6-14(9-15(13)17)23-11-12-4-2-1-3-5-12/h1-7,9-10,16,20H,8,11,19H2,(H,21,22)
InChI key:InChIKey=DFGNDJBYANKHIO-UHFFFAOYSA-N
SMILES:C(C(C(O)=O)N)C=1C=2C(NC1)=CC=C(OCC3=CC=CC=C3)C2
Synonyms:
  • (2S)-2-ammonio-3-[5-(benzyloxy)-1H-indol-3-yl]propanoate
  • 2-Amino-3-(5-(benzyloxy)-1H-indol-3-yl)propanoic acid
  • 2-Amino-3-(5-benzyloxy-1H-indol-3-yl)-propionic acid
  • 2-Amino-3-(5-phenylmethoxy-1H-indol-3-yl)propanoic acid
  • 2-Azaniumyl-3-(5-phenylmethoxy-1H-indol-3-yl)propanoate
  • 5-(Phenylmethoxy)-<span class="text-smallcaps">DL</span>-tryptophan
  • 5-(Phenylmethoxy)tryptophan
  • 5-Benzyloxy-<span class="text-smallcaps">DL</span>-tryptophan
  • 5-Benzyloxy-DL-tryptophane
  • 5-Benzyloxytryptophan
  • See more synonyms
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