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  • 1257853-32-9 , 2,2-二己基丙烷-1,3-二-b-D-吡喃葡萄糖苷, Octyl glucose neopentyl glycol;2,2-Dihexylpropane-1,3-bis b-D-glucopyranoside; Octyl MNG
1257853-32-9 , 2,2-二己基丙烷-1,3-二-b-D-吡喃葡萄糖苷, Octyl glucose neopentyl glycol;2,2-Dihexylpropane-1,3-bis b-D-glucopyranoside; Octyl MNG

1257853-32-9 , 2,2-二己基丙烷-1,3-二-b-D-吡喃葡萄糖苷, Octyl glucose neopentyl glycol;2,2-Dihexylpropane-1,3-bis b-D-glucopyranoside; Octyl MNG

1257853-32-9 , 2,2-二己基丙烷-1,3-二-BETA-D-吡喃葡萄糖苷,
Octyl glucose neopentyl glycol;2,2-Dihexylpropane-1,3-bis b-D-glucopyranoside; Octyl MNG,
Cas:1257853-32-9
C27H52O12 / 568.69
MFCD22124160

Octyl glucose neopentyl glycol

2,2-Dihexylpropane-1,3-bis b-D-glucopyranoside; Octyl MNG

2,2-二己基丙烷-1,3-二-BETA-D-吡喃葡萄糖苷,

Octyl glucose neopentyl glycol is a ubiquitin ligase inhibitor that prevents the ubiquitination and degradation of target proteins. It has been shown to inhibit protein synthesis in bacteria. Octyl glucose neopentyl glycol has been used to study the role of cytosolic proteins in emphysema. It was found that octyl glucose neopentyl glycol inhibits the production of these proteins by preventing the interaction between an ubiquitin-like protein and its substrate, thereby inhibiting protein synthesis. Octyl glucose neopentyl glycol also inhibits cancer cells by blocking fatty acid synthase, which is necessary for cell proliferation. This inhibitor can be used as a structural probe to determine enzyme-substrate interactions, such as those that occur with bacterial strain and protein synthesis. It can also be used to study the structure of proteins by exposing them to light or using inhibitors drugs.

Octyl Glucose Neopentyl Glycol (OGNG) is a nonionic surfactant that has gained significant attention in the field of research and industry. OGNG is a green alternative to traditional surfactants used in many applications, including personal care products, food additives, and pharmaceuticals. The surfactant's unique properties have led to various promising scientific investigations into its synthesis, characterization, and potential applications.

Synthesis and Characterization:

OGNG can be synthesized through the reaction of neopentyl glycol (NPG) and octyl glucoside (OG) in the presence of an acid catalyst. This reaction typically occurs at high temperature and pressure, resulting in high yields of OGNG.

Analytical Methods:

Various analytical methods have been used to study the properties and applications of OGNG. These methods include gas chromatography (GC), high-performance liquid chromatography (HPLC), and Fourier transform infrared (FT-IR) spectroscopy.

Biological Properties:

OGNG has been shown to have low toxicity in scientific experiments. It is biodegradable and poses little risk to the environment. However, further studies are necessary to fully understand the impact of OGNG in living organisms.

Toxicity and Safety in Scientific Experiments:

OGNG has been shown to have low toxicity in scientific experiments. It is biodegradable and poses little risk to the environment. However, further studies are necessary to fully understand the impact of OGNG in living organisms.

Applications in Scientific Experiments:

OGNG has shown potential applications in various fields of research and industry. These applications include the use of OGNG as a surfactant in personal care products, food additives, and pharmaceuticals. OGNG has also been studied as a potential drug delivery system due to its unique solubility properties.

Current State of Research:

Research into OGNG is ongoing, with scientists investigating its properties, synthesis methods, and potential applications. Recent research has focused on the use of OGNG in drug delivery systems and the development of novel uses of the surfactant in the field of materials science.

Potential Implications in Various Fields of Research and Industry:

OGNG has the potential to revolutionize many different fields of research and industry. Its unique properties have implications in various fields, including personal care products, food additives, and pharmaceuticals. OGNG is a green alternative to traditional surfactants, making it an attractive option for many different applications.

Limitations and Future Directions:

While OGNG has shown promising potential in various fields, there are limitations to its use. Further research is needed to fully understand the long-term effects of OGNG on living organisms and the environment. Future directions for research include investigating the use of OGNG in biodegradable plastics, as well as its potential as a catalyst in chemical reactions. Additionally, more research is needed to investigate the use of OGNG in drug delivery systems and the development of novel applications in the field of material science.

CAS Number1257853-32-9
Product NameOctyl Glucose Neopentyl Glycol
IUPAC Name(2S,3S,4R,5R,6S)-2-[2-hexyl-2-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]octoxy]-6-(hydroxymethyl)oxane-3,4,5-triol
Molecular FormulaC27H52O12
Molecular Weight568.69 g/mol
InChIInChI=1S/C27H52O12/c1-3-5-7-9-11-27(12-10-8-6-4-2,15-36-25-23(34)21(32)19(30)17(13-28)38-25)16-37-26-24(35)22(33)20(31)18(14-29)39-26/h17-26,28-35H,3-16H2,1-2H3/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26-/m0/s1
InChI KeyTYXCLOLHZMMLEK-RNDJEAJNSA-N
SMILESCCCCCCC(CCCCCC)(COC1C(C(C(C(O1)CO)O)O)O)COC2C(C(C(C(O2)CO)O)O)O
Canonical SMILESCCCCCCC(CCCCCC)(COC1C(C(C(C(O1)CO)O)O)O)COC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILESCCCCCCC(CCCCCC)(CO[C@@H]1[C@H]([C@@H]([C@H]([C@@H](O1)CO)O)O)O)CO[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)CO)O)O)O


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