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L-Tryptophan-[indole-2-13C]

General Information
Catalog: BLP-009354
CAS: 115709-68-7
Molecular Formula: C10[13C]H12N2O2
Molecular Weight: 205.22
Chemical Structure
L-Tryptophan-[indole-2-13C]
Description L-Tryptophan-[indole-2-13C] is a labelled L-Tryptophan. Tryptophan is an essential amino acid obtained from diet. Tryptophan is also a precursor of the neurotransmitter serotonin and the hormone melatonin.
Synonyms L-Tryptophan-(indole ring-2-13C)
Related CAS 73-22-3 (unlabelled)
Canonical SMILES C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N
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)/t9-/m0/s1/i6+1
InChI Key QIVBCDIJIAJPQS-XJBDPXLPSA-N
Melting Point 280-285°C (dec.) (lit.)
Purity 98% by HPLC; 98% atom 13C

L-Tryptophan-[indole-2-13C], a stable isotope-labeled compound, finds use in various research fields. Here are the key applications of L-Tryptophan-[indole-2-13C]:

Metabolic Tracing: Utilizing L-Tryptophan-[indole-2-13C] in metabolic studies allows researchers to delve into the intricate metabolic pathways of tryptophan within an organism. By meticulously monitoring the incorporation of the labeled carbon, scientists acquire insights into the kinetics and fluxes of tryptophan metabolism. This exploration aids in unraveling the biosynthesis of crucial metabolites such as serotonin and melatonin.

Protein Structure Analysis: In the realm of nuclear magnetic resonance (NMR) spectroscopy, this isotope-labeled tryptophan serves as a potent tool for the in-depth analysis of protein structure and dynamics. The 13C label imparts a unique signal, enabling a detailed scrutiny of tryptophan residues within protein frameworks. Such revelations are foundational in comprehending protein folding dynamics, interactions, and functional attributes.

Environmental and Ecological Research: Exploring the realms of ecology, L-Tryptophan-[indole-2-13C] can be harnessed to investigate nitrogen cycling and organic matter decomposition across diverse ecosystems. By introducing this tracer into soil or microbial communities, scientists can meticulously track the assimilation and transformation of tryptophan. This data yields invaluable insights into nutrient cycling dynamics and microbial activity in varying environmental settings.

Pharmaceutical Development: In the domain of drug research, L-Tryptophan-[indole-2-13C] plays a pivotal role in illuminating drug metabolism and pharmacokinetics. Incorporating the labeled tryptophan into experimental models enables researchers to monitor the interactions between the drug and metabolic pathways and identify any resulting metabolites. This knowledge forms the bedrock for evaluating drug efficacy and safety profiles.

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