104077-24-9

Basic information

• Product Name: 2,4-dinitrophenylaminocaproyltyrosine
• Synonyms: 2,4-dinitrophenylaminocaproyltyrosine
• CAS NO: 104077-24-9
• Molecular Formula: C21H24N4O8
• Molecular Weight: 0
• Mol File: 104077-24-9.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 784.9°Cat760mmHg
• Flash Point: 428.5°C
• Appearance: /
• Density: 1.418g/cm³
• Vapor Pressure: 5.92E-26mmHg at 25°C
• Refractive Index: 1.643
• CAS DataBase Reference: 2,4-dinitrophenylaminocaproyltyrosine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dinitrophenylaminocaproyltyrosine(104077-24-9)
• EPA Substance Registry System: 2,4-dinitrophenylaminocaproyltyrosine(104077-24-9)

Safety Data

• Hazardous Substances Data: 104077-24-9(Hazardous Substances Data)

Usage

Description

2,4-dinitrophenylaminocaproyltyrosine is a chemical compound derived from tyrosine, an amino acid present in proteins. It features a distinctive structure comprising a 2,4-dinitrophenyl group, an aminocaproyl group, and the tyrosine residue. 2,4-dinitrophenylaminocaproyltyrosine is recognized for its utility in bioconjugation and protein labeling studies, as well as in research focused on enzyme-substrate interactions. The unique structural attributes of 2,4-dinitrophenylaminocaproyltyrosine render it an invaluable tool for investigating the intricate relationships between proteins and other molecules within biological systems. Moreover, its characteristics hold promise for applications in drug development and medical research.

Uses

Used in Bioconjugation and Protein Labeling:
2,4-dinitrophenylaminocaproyltyrosine is utilized as a labeling agent for proteins, facilitating the study of protein interactions and dynamics. Its distinctive structure allows for the attachment of proteins to other molecules, making it a valuable tool in the field of molecular biology.
Used in Enzyme-Substrate Interaction Research:
In the realm of enzymology, 2,4-dinitrophenylaminocaproyltyrosine is employed as a model substrate to investigate the mechanisms of enzyme action. Its structure enables researchers to probe the specificity and catalytic properties of enzymes, contributing to a deeper understanding of enzymatic processes.
Used in Drug Development:
The properties of 2,4-dinitrophenylaminocaproyltyrosine have potential applications in the development of new pharmaceuticals. Its interaction with proteins and other biological molecules could be harnessed to design drugs that target specific biological pathways, potentially leading to novel therapeutic strategies.
Used in Medical Research:
2,4-dinitrophenylaminocaproyltyrosine is also used as a research compound in medical studies, where its interactions with biological systems can provide insights into disease mechanisms and potential therapeutic interventions. Its versatility in binding to various molecules makes it a promising candidate for exploring new avenues in medical science.

InChI:InChI=1/C21H24N4O8/c26-16-8-5-14(6-9-16)12-18(21(28)29)23-20(27)4-2-1-3-11-22-17-10-7-15(24(30)31)13-19(17)25(32)33/h5-10,13,18,22,26H,1-4,11-12H2,(H,23,27)(H,28,29)/t18-/m0/s1