• Verification code
  • Optimal Prices
    Buying products on this site guarantees the best price
  • Flexible Batches
    Flexible batch size to meet different needs of global customers
  • Prompt Delivery
    Warehouses in multiple cities to ensure timely delivery
  • Quality Assurance
    Strict process parameter control to ensure product quality
  • One-to-one Customization
    One-to-one custom synthesis for special structural needs

L-Tryptophan (Ring-[13C6])

General Information
Catalog: BLP-004301
Molecular Formula: C5[13C]6H12N2O2
Molecular Weight: 210.18
Chemical Structure
L-Tryptophan (Ring-[13C6])
Description L-Tryptophan (Ring-[13C6]) is the labelled form of L-Tryptophan, which is an essential amino acid.
Synonyms L-Tryptophan (Ring-13C6); L-Tryptophan-13C6; (2S)-2-amino-3-(1H-indol-3-yl)propanoic acid-13C6
IUPAC Name (2S)-3-[(3a,4,5,6,7,7a-13C6)-1H-indol-3-yl]-2-aminopropanoic acid
Related CAS 73-22-3 (unlabelled)
Purity 98% by CP

L-Tryptophan (Ring-[13C6]), an isotopically labeled amino acid widely utilized in biochemical research and analysis, finds versatile applications in various fields. Here are key applications of L-Tryptophan (Ring-[13C6]) presented with high perplexity and burstiness:

Metabolic Tracing: Delving into metabolic tracing studies, researchers employ L-Tryptophan (Ring-[13C6]) to investigate the intricate pathways of tryptophan metabolism. By meticulously tracking the 13C-labeled carbon atoms, they unravel the complex metabolic destiny of tryptophan in cells and tissues. This exploration sheds light on disorders like tryptophan malabsorption and unveils the pivotal role of tryptophan in neurotransmitter synthesis.

Structural Biology: Within the realm of structural biology, L-Tryptophan (Ring-[13C6]) serves as a cornerstone for NMR (nuclear magnetic resonance) spectroscopy studies. The isotopic enrichment offers a window into the detailed examination of tryptophan residues within proteins, aiding in unraveling the intricacies of protein structure and dynamics. By leveraging this tool, researchers glean insights into protein folding, conformational changes, and interactions with other biomolecules.

Protein-Protein Interaction Studies: In the realm of protein-protein interactions, L-Tryptophan (Ring-[13C6]) plays a pivotal role by integrating the labeled amino acid into target proteins. This labeled tryptophan serves as a discerning reporter, pinpointing interaction sites and binding interfaces through techniques such as fluorescence spectroscopy and mass spectrometry. These studies are instrumental in unraveling cellular pathways and laying the groundwork for designing targeted therapeutic interventions.

Nutritional Research: In the domain of nutritional research, L-Tryptophan (Ring-[13C6]) emerges as a valuable tool for assessing the bioavailability and digestion of dietary tryptophan. Researchers delve into understanding how the body metabolizes and utilizes tryptophan from diverse dietary sources by quantifying the 13C isotopic enrichment in biological samples. This knowledge plays a pivotal role in shaping dietary recommendations and deepening our understanding of the nutritional implications of tryptophan intake.

Interested in our Service & Products?
Need detailed information?

USA
  • International: 1-631-504-6093
  • US & Canada (Toll free): 1-844-BOC(262)-0123
  • 45-16 Ramsey Road, Shirley, NY 11967, USA
  • Email: info@bocsci.com
  • Fax: 1-631-614-7828
UK
  • 44-20-3286-1088
  • 85 Great Portland Street, London, W1W 7LT
  • Email: info@bocsci.com
Copyright © 2025 BOC Sciences. All Rights Reserved.
0
Inquiry Basket

No data available, please add!

Delete selectedGo to checkout

We use cookies to understand how you use our site and to improve the overall user experience. This includes personalizing content and advertising. Read our Privacy Policy

Accept Cookies
x