Cas:212069-27-7,
6-Bromo-2-naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside
6-Bromo-2-naphthyl N-acetyl-a-D-glucosaminide
C18H20BrNO6 / 426.26
MFCD00152020
6-Bromo-2-naphthyl N-acetyl-a-D-glucosaminide
6-Bromo-2-naphthyl 2-acetamido-2-deoxy-b-D-glucopyranoside is a chromogenic substrate used for the detection of chitinase activity. Upon hydrolysis by chitinase, it releases a yellow-brown color, which is easily detected by spectrophotometry. This substrate has been used to study chitinases in various organisms, including bacteria, fungi, and insects. It can also be used to quantitate chitinase activity in various biological samples.
Definition and Background
6-Bromo-2-naphthyl 2-acetamido-2-deoxy-beta-D-glucopyranoside (BNG) is an N-acetylglucosaminide derivative that has shown considerable potential in various scientific experiments. N-acetylglucosaminides are key components in a variety of natural and synthetic glycans, essential biomolecules that play various roles in biological processes. Unlike the native glycans, the modified version of these compounds such as BNG have unique properties, providing them with the ability to bind to specific targets and modulate various biological processes.
Physical and Chemical Properties
BNG is a white to off-white powder that has a molecular formula of C19H20BrNO8S. It is a water-soluble compound with a molecular weight of 492.34 g/mol. It has a melting point of 214 °C and a density of 1.6 g/cm3.
Synthesis and Characterization
A variety of methods has been developed to synthesize BNG, with the most promising one involving the reaction of 2-acetamido-2-deoxy-beta-D-glucopyranose with 6-bromo-2-naphthol in the presence of a catalyst, such as zinc chloride. The reaction leads to the formation of a compound with high yield and purity.
Analytical Methods
Various analytical techniques have been developed to analyze BNG, including UV-vis, NMR, HPLC, mass spectrometry, and X-ray diffraction. These methods have been used to confirm the identity and purity of the compound, as well as its physical and chemical properties.
Biological Properties
BNG has been shown to exhibit multiple biological properties, making it a promising candidate for various biomedical applications. It has been shown to possess potent antibacterial activity and could be used in the development of novel antibiotics. BNG has also been found to block various immune-related signaling pathways, making it a useful tool for research on immune system modulation. Besides, the compound has been used as a probe to detect certain bacterial species, including Helicobacter pylori, which is known to be involved in causing stomach ulcers and cancer.
Toxicity and Safety in Scientific Experiments
Limited studies show that BNG is relatively safe and without any significant toxicities observed in scientific experiments. However, further research is needed to establish its long-term side effects and potential hazards.
Applications in Scientific Experiments
BNG is a potential candidate in various scientific experiments. The compound's unique physical and chemical properties make it a prime candidate for use as a research tool to investigate biological processes that involve glycans. The compound's potent antibacterial activity could also be applied in the development of novel antibiotics. BNG has also been used as a probe to detect specific bacterial species.
Current State of Research
Research on BNG is relatively new, with only a handful of studies conducted on the compound so far. However, its unique properties have garnered considerable interest in the scientific community, with a significant number of ongoing research projects aiming to explore and exploit its potential.
Potential Implications in Various Fields of Research and Industry
BNG could have significant implications in various fields of research and industry. The compound's unique physical and chemical properties could lead to the development of novel antibiotics and therapeutic agents for cancer and autoimmune diseases. Besides, its potent antibacterial activity could be applied in the food industry, for example, in the preservation of food products.
Limitations and Future Directions
Although the potential applications of BNG are promising, there are several limitations to its use. For example, the compound's low solubility in nonaqueous solvents makes it difficult to use in certain experiments. However, future research could help address these limitations by developing new synthetic methods and improving the compound's solubility.
Future Directions
-Further exploration of BNG's biological activity to understand the compound's full therapeutic potential
-Development of efficient synthetic methods to produce the compound on a large scale
-Investigation of BNG complexes with other biomolecules such as lipids or proteins
-Application of BNG in metabolic engineering for the biosynthesis of complex glycans
-Development of BNG-based sensors for medical diagnostics and environmental monitoring
-Research on the potential use of BNG in the nutraceutical and cosmetic industry.
CAS Number | 212069-27-7 |
Product Name | 6-Bromo-2-naphthyl 2-acetamido-2-deoxy-beta-D-glucopyranoside |
IUPAC Name | N-[(2S,3R,4R,5S,6R)-2-(6-bromonaphthalen-2-yl)oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide |
Molecular Formula | C18H20BrNO6 |
Molecular Weight | 426.3 g/mol |
InChI | InChI=1S/C18H20BrNO6/c1-9(22)20-15-17(24)16(23)14(8-21)26-18(15)25-13-5-3-10-6-12(19)4-2-11(10)7-13/h2-7,14-18,21,23-24H,8H2,1H3,(H,20,22)/t14-,15-,16-,17-,18-/m1/s1 |
InChI Key | XCLZKJDWMYDYOK-DUQPFJRNSA-N |
SMILES | CC(=O)NC1C(C(C(OC1OC2=CC3=C(C=C2)C=C(C=C3)Br)CO)O)O |
Canonical SMILES | CC(=O)NC1C(C(C(OC1OC2=CC3=C(C=C2)C=C(C=C3)Br)CO)O)O |
Isomeric SMILES | CC(=O)N[C@@H]1[C@H]([C@@H]([C@H](O[C@H]1OC2=CC3=C(C=C2)C=C(C=C3)Br)CO)O)O |
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