L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate
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L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate

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Category
L-Amino Acids
Catalog number
BAT-002149
CAS number
201851-46-9
Molecular Formula
C16H20N4O4·C2HF3O2
Molecular Weight
446.38
L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate
IUPAC Name
(2S)-2-amino-5-(carbamoylamino)-N-(4-methyl-2-oxochromen-7-yl)pentanamide;2,2,2-trifluoroacetic acid
Synonyms
(S)-2-Amino-N-(4-methyl-2-oxo-2H-chromen-7-yl)-5-ureidopentanamide 2,2,2-trifluoroacetate; H-Cit-AMC yenTFA
Storage
Store at -20 °C
InChI
InChI=1S/C16H20N4O4.C2HF3O2/c1-9-7-14(21)24-13-8-10(4-5-11(9)13)20-15(22)12(17)3-2-6-19-16(18)23;3-2(4,5)1(6)7/h4-5,7-8,12H,2-3,6,17H2,1H3,(H,20,22)(H3,18,19,23);(H,6,7)/t12-;/m0./s1
InChI Key
SMVDPONOBWXIKK-YDALLXLXSA-N
Canonical SMILES
CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C(CCCNC(=O)N)N.C(=O)(C(F)(F)F)O

L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate, a versatile biochemical compound with diverse bioscience applications, spans across various fields. Here are four key applications of L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate:

Diagnostic Assays: Spearheading diagnostic innovation, L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate assumes a central role in assays targeting the enzymatic activity of specific enzymes like arginase and nitric oxide synthase. In these assays, the compound acts as a fluorogenic substrate that, upon enzymatic cleavage, emits a fluorescent product. This product, measurable through spectrometry, enables precise monitoring of enzyme activity, crucial for diagnosing a spectrum of diseases and medical conditions.

Drug Development: In the arena of pharmaceutical exploration, L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate emerges as a pivotal element in assessing the efficacy and selectivity of enzyme inhibitors. Operating as a substrate in studies of enzyme kinetics, it offers researchers a glimpse into how potential drugs interact with target enzymes. This understanding is essential for the development of novel therapeutic agents aimed at modulating enzyme activity effectively and with precision.

Cell Biology: Within the intricate realm of cell biology, this compound acts as a linchpin for unraveling cellular pathways associated with citrulline metabolism and its associated enzymes. Researchers leverage this compound to probe the effects of changes in enzyme activity on cellular processes, such as nitric oxide production. This exploration aids in deciphering disease mechanisms linked to shifts in citrulline metabolism, particularly those observed in cardiovascular diseases, illuminating potential avenues for therapeutic interventions.

Biochemical Studies: Delving deep into the intricacies of biochemistry, L-Citrulline 7-amido-4-methylcoumarin trifluoroacetate emerges as a cornerstone for dissecting reaction mechanisms and unraveling enzyme structure-function relationships. By providing insights into the dynamic nature of enzymes, it fortifies efforts in structural biology and assists in designing synthetic biocatalysts. This compound serves as an indispensable tool for fundamental explorations and applied bioscience endeavors, pushing the frontiers of biochemical understanding and practical applications.

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