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N-Acetyl-L-tryptophan-[indole-d5]

General Information
Catalog: BLP-009916
Molecular Formula: C13D5H9N2O3
Molecular Weight: 251.29
Chemical Structure
N-Acetyl-L-tryptophan-[indole-d5]
Description N-Acetyl-L-tryptophan-[indole-d5] is a labelled N-Acetyl-L-tryptophan, an NK-1R inhibitor.
IUPAC Name (2S)-2-acetamido-3-(2,4,5,6,7-pentadeuterio-1H-indol-3-yl)propanoic acid
Related CAS 1218-34-4 (unlabelled)
Canonical SMILES CC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O
InChI InChI=1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)/t12-/m0/s1/i2D,3D,4D,5D,7D
InChI Key DZTHIGRZJZPRDV-VMOXMFORSA-N
Purity 97% by HPLC; 98% atom D

N-Acetyl-L-tryptophan-[indole-d5], a stable isotope-labeled compound utilized primarily in bioscience research, possesses diverse applications in the realm of scientific inquiry. Here are key applications presented with a high degree of perplexity and burstiness:

Stable Isotope Tracing: Within the domain of metabolic research, N-Acetyl-L-tryptophan-[indole-d5] emerges as a pivotal tool for elucidating tryptophan metabolism. By integrating this labeled compound into biological systems, researchers embark on a journey to unravel intricate metabolic pathways and quantify metabolites using cutting-edge mass spectrometry techniques. This methodological approach grants researchers profound insights into metabolic fluxes, illuminating the path to comprehensive understanding of disorders linked to tryptophan metabolism.

Pharmacokinetics Studies: Delving into the realm of pharmacokinetics, N-Acetyl-L-tryptophan-[indole-d5] takes center stage in exploring the absorption, distribution, metabolism, and excretion (ADME) of tryptophan derivatives. Leveraging stable isotopes, this compound enables a clear demarcation between endogenous and exogenous compounds, furnishing precise measurements in biological samples. This nuanced information forms the cornerstone of drug development and offers a lens to comprehend the intricate processes through which tryptophan-based therapies navigate the labyrinthine pathways of the human body.

Protein Structure and Dynamics: In the intricate landscape of structural biology, N-Acetyl-L-tryptophan-[indole-d5] assumes a pivotal role, seamlessly integrating into proteins to expedite NMR spectroscopy studies. The deuterium labeling bestows enhanced spectral resolution, affording researchers an unparalleled opportunity to delve into the minutiae of protein folding and dynamics. These in-depth studies not only shed light on protein function, interactions, and stability, but also unveil the intricacies of these biological entities under a myriad of environmental conditions, paving the way for groundbreaking discoveries in the realm of molecular biology.

Analytical Chemistry: Positioned as an internal standard in the quantitative analysis of tryptophan and its metabolites, N-Acetyl-L-tryptophan-[indole-d5] boasts paramount importance in the domain of analytical chemistry. Its seamless incorporation into assays guarantees precise and accurate measurements, nullifying variations in sample preparation and instrument conditions. This meticulous attention to detail ensures the production of reliable data, thereby underpinning the foundations of both clinical diagnostics and cutting-edge research endeavors, ushering in a new era of analytical precision and scientific excellence.

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