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  • 99792-79-7 , Chlorophenol red b-D-galactopyranoside,CPRG
99792-79-7 , Chlorophenol red b-D-galactopyranoside,CPRG

99792-79-7 , Chlorophenol red b-D-galactopyranoside,CPRG

99792-79-7 , Chlorophenol red b-D-galactopyranoside,CPRG
C25H22Cl2O10S / 585.41
MFCD05863726

Chlorophenol red b-D-galactopyranoside,CPRG

Chlorophenol red b-D-galactopyranoside (CPRG) is an element used in biological studies as a chromogenic substrate for β-galactosidase. CPRG is a synthetic compound that can be used to measure the activity of the enzyme and to measure the activity of recombinant proteins. It has been used in polymerase chain reactions, as an enzyme substrate, and as a transistor capacitor in pixel displays. CPRG has also been shown to have genotoxic activity when exposed to radiation or other forms of protein damage.

Chlorophenol red galactopyranoside (CPRG) is a chemical compound that is extensively used as a substrate in a variety of scientific experiments. CPRG is a dye that changes color based on the presence or absence of beta-galactosidase enzyme activity. This reaction has found wide applications in molecular biology, biochemistry, and microbiology. In this paper, we will explore the definition and background of CPRG, its physical and chemical properties, synthesis and characterization methods, analytical methods, biological properties, toxicity and safety concerns, applications in scientific experiments, current research, potential implications in various fields of research and industry, and limitations and future directions.

Definition and Background:

CPRG, also known as 5-chloro-2-(2,4-dinitroanilino)-2,3,5,6-tetrahydro-6-benzothiazolyl-3-(β-D-galactopyranoside), is a chemical indicator used in a variety of scientific experiments. CPRG is an analog of X-gal, and it is a chromogenic substrate that, when acted on by beta-galactosidase, changes color from colorless to yellow. This reaction is widely used in molecular biology, biochemistry, and microbiology as a vital tool for the detection and quantification of enzyme activity in a sample.

Physical and Chemical Properties:

CPRG is a yellowish to beige crystalline powder that is soluble in water and methanol. Its melting point is 206–207 °C, and its purity can range from 97% to 99%. CPRG is highly stable under normal conditions, and it has a shelf life of several years when stored in a cool and dry place.

Synthesis and Characterization:

CPRG can be synthesized by coupling the chlorophenol red with β-D-galactopyranoside in the presence of a coupling agent like 1-ethyl-3-[3-dimethylaminopropyl] carbodiimide (EDC). The reaction produces CPRG, dicyclohexylurea, and water as by-products. The synthesized compound is characterized using analytical techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR), and infrared (IR) spectroscopy.

Analytical Methods:

CPRG is used as a substrate in various assays to determine β-galactosidase enzyme activity. The assay can be carried out in a microplate reader, spectrophotometer, or fluorometer. The CPRG substrate is added to the sample, and the reaction is allowed to proceed for a specific amount of time. The color change is then monitored at a specific wavelength.

Biological Properties:

CPRG is not metabolized by the cellular system and does not exhibit cytotoxic effects on cells or tissues. However, the yellow color of the compound can interfere with other colorimetric assays, and care should be taken when interpreting results.

Toxicity and Safety in Scientific Experiments:

CPRG is generally considered safe for use in scientific experiments when handled according to standard laboratory protocols. However, ingestion, inhalation, or skin contact of the compound can cause irritation and should be avoided. Proper personal protective equipment, such as gloves and safety goggles, should be worn while handling the compound.

Applications in Scientific Experiments:

The CPRG reaction is widely used in molecular biology, biochemistry, and microbiology to detect and quantify β-galactosidase activity. The assay is used to monitor gene expression, protein function, and enzyme kinetics. CPRG can also be used to detect bacterial contamination in food and water samples.

Current State of Research:

The use of CPRG in scientific experiments has been well established, and its applications continue to develop. Recent research has focused on the development of new substrates that can be used in conjunction with CPRG to expand its applications.

Potential Implications in Various Fields of Research and Industry:

The potential applications of CPRG are vast and varied. The compound can be used in gene expression studies, protein purification, and drug discovery. The assay can be adapted for high-throughput screening, which can accelerate drug discovery processes. CPRG can be used to detect bacterial contamination in food and water samples, which can have significant implications for the food and beverage industry.

Limitations and Future Directions:

Although CPRG is widely used in scientific experiments, there are some limitations to its use. The assay requires the presence of β-galactosidase enzyme activity, which limits its applicability in samples with low enzyme expression. Future research can focus on the development of new substrates that can detect other enzymes or metabolic processes. Moreover, researchers can explore the use of CPRG in vivo imaging applications.

Future Directions:

1. Development of new substrates that can detect other enzymes or metabolic processes.

2. Exploration of the use of CPRG in vivo imaging applications.

3. Investigation of the potential use of CPRG in clinical diagnosis.

4. Development of rapid detection methods for bacterial contamination in food and water samples.

5. Investigation of the use of CPRG as a tool for studying enzyme-substrate interactions.

6. Development of modified CPRG substrates that can be used to study signal transduction pathways.

7. Development of high-throughput screening methods using CPRG-based assays.

8. Investigation of the use of CPRG as a tool for studying protein-protein interactions.

9. Development of CPRG-prodrug conjugates for enhanced drug delivery.

10. Investigation of the use of CPRG in antibiotic discovery and drug resistance studies.

CAS Number99792-79-7
Product NameChlorophenol red galactopyranoside
IUPAC Name(2S,3R,4S,5R,6R)-2-[2-chloro-4-[3-(3-chloro-4-hydroxyphenyl)-1,1-dioxo-2,1λ6-benzoxathiol-3-yl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC25H22Cl2O10S
Molecular Weight585.4 g/mol
InChIInChI=1S/C25H22Cl2O10S/c26-15-9-12(5-7-17(15)29)25(14-3-1-2-4-20(14)38(33,34)37-25)13-6-8-18(16(27)10-13)35-24-23(32)22(31)21(30)19(11-28)36-24/h1-10,19,21-24,28-32H,11H2/t19-,21+,22+,23-,24-,25?/m1/s1
InChI KeyUYYRDZGZGNYVBA-VPXCCNNISA-N
SMILESC1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC(=C(C=C3)O)Cl)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)Cl
Synonymschlorophenol red beta-D-galactopyranoside, chlorophenol red galactopyranoside, CPRG
Canonical SMILESC1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC(=C(C=C3)O)Cl)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)Cl
Isomeric SMILESC1=CC=C2C(=C1)C(OS2(=O)=O)(C3=CC(=C(C=C3)O)Cl)C4=CC(=C(C=C4)O[C@H]5[C@@H]([C@H]([C@H]([C@H](O5)CO)O)O)O)Cl


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