Welcome: Chemsynlab ,carbohydrate chemistry
Language: Chinese ∷  English

1022-79-3 , 5-Bromo-2-deoxyuridine, CAS:1022-79-3

1022-79-3 , 5-Bromo-2-deoxyuridine,
CAS:1022-79-3
C9H12BrN3O4 / 306.11
MFCD00047496

5-溴-2-脱氧胞苷, 5-Bromo-2-deoxyuridine

5-Bromo-2'-deoxycytidine is a synthetic nucleoside analogue that is used to treat diabetic neuropathy. It is structurally similar to cytidine, and inhibits the enzyme DNA polymerase by intramolecular catalysis. This causes deamination of the 5-bromo group, which prevents further synthesis of DNA. 5-Bromo-2'-deoxycytidine has been shown to be effective in vivo in a mouse model for inflammatory bowel diseases, including colitis and eosinophilic enteritis. The drug was also found to inhibit the production of Eosinophil peroxidase from HL-60 cells in vitro.

5-Bromo-2’-deoxycytidine (BrdC) is a nucleoside analog that is incorporated into DNA during replication. This nucleoside analog can inhibit the DNA methylation process, making it a potentially useful tool in research related to epigenetics, gene expression, and cancer.

Synthesis and Characterization

BrdC can be synthesized by extensively modifying the cytosine nucleoside using a range of techniques. The final product can be characterized using analytical methods such as nuclear magnetic resonance (NMR), ultraviolet-visible (UV-Vis) spectroscopy, or mass spectrometry (MS).

Analytical Methods

BrdC can be detected using various analytical techniques, including high-performance liquid chromatography (HPLC), NMR, and MS. HPLC can be used to separate BrdC from other compounds in a sample, while NMR and MS can be used to determine the purity of the sample.

Biological Properties

BrdC has been shown to be an inhibitor of the DNA methylation process. It can also be incorporated into DNA during replication, acting as a possible mutagen and reducing the stability of the DNA strand. However, some studies have suggested that BrdC could have a therapeutic effect on certain types of cancer.

Toxicity and Safety in Scientific Experiments

In studies using BrdC, it has been shown to be generally safe and non-toxic. However, it is important to use the appropriate safety precautions when handling this compound due to its potential mutagenic properties.

Applications in Scientific Experiments

BrdC has been used in a range of scientific experiments, including studies on epigenetics, gene expression, and cancer. It can be used to inhibit DNA methylation or as an analog for DNA replication.

Current State of Research

Research on BrdC has been ongoing for several years, with studies exploring its potential uses in cancer therapy and epigenetic modification. Additional research is needed to fully understand the potential benefits and limitations of this nucleoside analog.

Potential Implications in Various Fields of Research and Industry

BrdC has potential applications in various fields of research, including cancer therapy, epigenetic modification, and gene expression regulation. It could also have industrial applications, such as in the production of synthetic DNA or genetic engineering.

Limitations and Future Directions

One of the limitations of BrdC is that it can be mutagenic and affect the stability of the DNA strand. Additionally, it is important to use the appropriate safety precautions when handling this compound due to its potential mutagenic properties. Future directions for research include exploring the potential therapeutic uses of BrdC in cancer treatment, as well as studying its effects on epigenetic modification and gene expression regulation.

Some potential future directions for research on BrdC include:

1. Investigating the use of BrdC in combination with other drugs for cancer therapy

2. Studying the effect of BrdC on different cancer cell lines

3. Exploring the potential use of BrdC in gene therapy

4. Enhancing the synthesis methods for BrdC to improve purity and yield

5. Developing new analytical methods for detecting BrdC in complex biological samples

6. Investigating the potential industrial applications of BrdC, such as in DNA synthesis or genetic engineering.

CAS Number1022-79-3
Product Name5-Bromo-2'-deoxycytidine
IUPAC Name4-amino-5-bromo-1-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one
Molecular FormulaC9H12BrN3O4
Molecular Weight306.11 g/mol
InChIInChI=1S/C9H12BrN3O4/c10-4-2-13(9(16)12-8(4)11)7-1-5(15)6(3-14)17-7/h2,5-7,14-15H,1,3H2,(H2,11,12,16)/t5-,6+,7+/m0/s1
InChI KeyKISUPFXQEHWGAR-RRKCRQDMSA-N
SMILESC1C(C(OC1N2C=C(C(=NC2=O)N)Br)CO)O
Synonyms5 Bromo 2' Deoxycytidine, 5-Bromo-2'-Deoxycytidine, Bromodeoxycytidine
Canonical SMILESC1C(C(OC1N2C=C(C(=NC2=O)N)Br)CO)O
Isomeric SMILESC1[C@@H]([C@H](O[C@H]1N2C=C(C(=NC2=O)N)Br)CO)O


CAS No: 1022-79-3 Synonyms: 5-Bromo-2'-deoxy-D-cytidine MDL No: MFCD00047496 Chemical Formula: C9H12BrN3O4 Molecular Weight: 306.11
References: 1. Sanders PG, Wilkie NM, Davison AJ, J. Gen. Virol. 1982, Vol63, p277-295


INQUIRY

Scan the qr codeClose
the qr code