L-Citrulline 7-amido-4-methylcoumarin hydrobromide
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L-Citrulline 7-amido-4-methylcoumarin hydrobromide

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Category
L-Amino Acids
Catalog number
BAT-002219
CAS number
201851-45-8
Molecular Formula
C16H21BrN4O4
Molecular Weight
413.27
IUPAC Name
(2S)-2-amino-5-(carbamoylamino)-N-(4-methyl-2-oxochromen-7-yl)pentanamide;hydrobromide
Synonyms
H-Cit-AMC HBr; H-Orn(Carbamoyl)-AMC HBr; N-δ-Carbamoyl-L-ornithine 7-amido-4-methylcoumarin hydrobromide
Storage
Store at 2-8 °C
InChI
InChI=1S/C16H20N4O4.BrH/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;/h4-5,7-8,12H,2-3,6,17H2,1H3,(H,20,22)(H3,18,19,23);1H/t12-;/m0./s1
InChI Key
XYOHUMXDURSJOW-YDALLXLXSA-N
Canonical SMILES
CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C(CCCNC(=O)N)N.Br

L-Citrulline 7-amido-4-methylcoumarin hydrobromide, a synthetic compound with diverse applications in biochemical and biomedical research, is harnessed across various scientific domains. Here are four key applications:

Enzyme Activity Assays: A cornerstone of enzyme activity assays, L-Citrulline 7-amido-4-methylcoumarin hydrobromide takes center stage in assessing the functionality of enzymes like arginase. Through enzymatic hydrolysis, it generates a fluorescent compound, enabling researchers to quantitatively evaluate enzyme activity in diverse samples. This method proves invaluable for probing enzyme kinetics and executing screenings for potential enzyme inhibitors, delving into the nuanced intricacies of enzymatic processes.

Drug Development: Integral to drug development endeavors, this compound plays a pivotal role in screening for potential arginase inhibitors. Leveraging high-throughput screening assays with L-Citrulline 7-amido-4-methylcoumarin hydrobromide, pharmaceutical researchers identify compounds capable of modulating enzyme activity effectively. This sophisticated process lays the groundwork for crafting novel therapeutic agents targeting complex conditions like cardiovascular diseases and cancer.

Biochemical Pathway Analysis: Scientists exploit the potential of L-Citrulline 7-amido-4-methylcoumarin hydrobromide to probe intricate biochemical pathways associated with arginase and nitric oxide production. By unraveling the multifaceted role of this enzyme in cellular processes, researchers shed light on the mechanisms underpinning a myriad of physiological and pathological states. This profound knowledge serves as a cornerstone for devising precise interventions in metabolic and vascular disorders.

Fluorescence Microscopy: Harnessing the fluorescent properties of L-Citrulline 7-amido-4-methylcoumarin hydrobromide, researchers delve into the dynamic realms of cellular biology through fluorescence microscopy studies. By employing this compound as a substrate in live-cell imaging, researchers achieve real-time visualization of enzymatic activities, unlocking a realm of cellular processes with unparalleled precision. This cutting-edge technique empowers researchers to map out spatial distributions of enzymatic activity and delve into intracellular dynamics.

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