Biophen CS 01(81) presents a peptide-like scaffold designed for in vitro biochemical measurements, particularly protease or coagulation studies. Residue configuration influences substrate accessibility and charge distribution. Researchers use it to examine cleavage kinetics and interaction specificity. Applications include enzymatic profiling, method validation, and biophysical analysis.
CAT No: PI-021
CAS No:86890-95-1
Synonyms/Alias:86890-95-1;N-P-Tosyl-Gly-Pro-Arg P-nitroanilide acetate salt;N-(p-Tosyl)-GPR-pNA acetate;N-(p-Tosyl)-GPR-pNA (acetate);acetic acid;(2S)-N-[(2S)-5-(diaminomethylideneamino)-1-(4-nitroanilino)-1-oxopentan-2-yl]-1-[2-[(4-methylphenyl)sulfonylamino]acetyl]pyrrolidine-2-carboxamide;Thrombin Substrate I;Biophen CS 01(81);SCHEMBL3507728;NGXDRWVTRQRSED-VROPFNGYSA-N;AKOS024436556;AKOS032957197;AKOS040755540;FT172225;TS-08858;HY-138143;CS-0145492;NS00066176;N-p-tosyl-gly-pro-argp-nitroanilideacetatesalt;N-(p-tosyl)-gly-pro-arg-p-nitroanilide acetate salt;N-(p-Tosyl)-Gly-Pro-Arg p-nitroanilide acetate salt, thrombin substrate;(S)-N-((S)-5-guanidino-1-(4-nitrophenylamino)-1-oxopentan-2-yl)-1-(2-(4-methylphenylsulfonamido)acetyl)pyrrolidine-2-carboxamide acetate;
Biophen CS 01(81) is a specialized carbohydrate compound developed to support advanced research in the fields of biochemistry, glycobiology, and molecular biology. This product is characterized by its unique carbohydrate structure, making it an essential tool for scientists investigating glycan interactions, enzymatic processes, and cellular communication pathways. Engineered for high solubility and consistent performance, Biophen CS 01(81) offers reliable results in a variety of laboratory settings, facilitating the study of carbohydrate-related mechanisms with precision and reproducibility. Its versatility and compatibility with a wide array of experimental protocols make it a preferred choice for researchers aiming to unravel the complexities of carbohydrate functions in biological systems.
Glycobiology Research: Biophen CS 01(81) serves as a pivotal reagent in glycobiology, where it is utilized to explore the structure, function, and biosynthesis of glycans. By providing a defined carbohydrate substrate, it enables researchers to dissect glycan-mediated cellular processes, including cell adhesion, signal transduction, and immune recognition. Its application in glycosylation studies helps elucidate the roles of specific carbohydrate motifs in protein folding and stability, advancing our understanding of post-translational modifications and their implications in health and disease.
Enzyme Assays: In the context of enzymology, Biophen CS 01(81) is frequently employed as a substrate to assess the activity and specificity of glycosidases, glycosyltransferases, and other carbohydrate-processing enzymes. The compound's well-defined structure allows for precise kinetic measurements and mechanistic studies, supporting the development of enzyme inhibitors or activators. This application is critical for mapping enzymatic pathways and for the screening of potential modulators that could influence carbohydrate metabolism in various biological systems.
Cell Signaling Studies: The compound also plays a significant role in cell signaling research, particularly in investigations focused on glycan-mediated communication between cells. By incorporating Biophen CS 01(81) into cell culture experiments, scientists can monitor how specific carbohydrate structures influence receptor activation, downstream signaling cascades, and cellular responses. Such studies are invaluable for identifying novel signaling mechanisms and for understanding how alterations in glycan patterns may contribute to pathological conditions.
Lectin Binding Analysis: Biophen CS 01(81) is an important tool for lectin binding assays, which are designed to characterize the interactions between carbohydrates and lectin proteins. By serving as a target or competitor in these assays, it facilitates the identification of lectin binding preferences and affinities, thereby supporting the mapping of glycan-lectin networks in both normal and diseased tissues. This information is essential for advancing research into cell recognition, pathogen-host interactions, and immune system modulation.
Microbial Glycobiology: In the realm of microbiology, Biophen CS 01(81) is utilized to study the carbohydrate-mediated processes that underpin microbial adhesion, colonization, and biofilm formation. By mimicking natural glycan structures, it enables researchers to investigate how microbes interact with host tissues and surfaces, providing insights into infection mechanisms and potential intervention strategies. This application is particularly valuable for the development of antimicrobial agents that target carbohydrate-dependent pathways.
Biophen CS 01(81) thus stands as a multifaceted carbohydrate compound that significantly enhances research capabilities across multiple scientific disciplines. Its application in glycobiology, enzymology, cell signaling, lectin binding, and microbial studies underscores its importance as a foundational reagent for dissecting carbohydrate-related phenomena. As researchers continue to uncover the intricate roles of glycans in biology, Biophen CS 01(81) will remain an indispensable asset, enabling the pursuit of novel discoveries and the advancement of knowledge in carbohydrate science.
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