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Catalog No: A10GD-4744
Cas No: 71676-30-7
Properties: Mol Formula: C19H20O5S, Mol Weight: 360.4
IUPAC Name: (4aR,6S,7R,8R,8aS)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol
Synonym: PHENYL4,6-O-BENZYLIDENE-1-THIO-BETA-D-GLUCOPYRANOSIDE, (4aR,6S,7R,8R,8aS)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol, SCHEMBL18523269
Phenyl 4,6-O-benzylidene-1-thio-beta-D-glucopyranoside is a compound that has received significant attention in the field of medicinal chemistry due to its potential therapeutic applications. This paper aims to provide an overview of the current state of research on the subject, examining its properties, synthesis and characterization, analytical methods, biological properties, toxicology and safety, applications, and future directions for research.
Definition and Background:
Phenyl 4,6-O-benzylidene-1-thio-beta-D-glucopyranoside is a chemical compound that belongs to the class of thio-glucosides. The molecule has a molecular formula of C19H20O5S and a molecular weight of 360.42g/mol. Also known as PTG, this molecule has shown promise as an antitumor and anti-inflammatory agent.
Physical and Chemical Properties:
PTG is a white powder that is insoluble in water but soluble in organic solvents such as chloroform and methanol. The compound has a crystalline structure and a density of 1.34 g/cm^3. It is relatively stable under normal conditions but can be decomposed under acidic or basic conditions.
Synthesis and Characterization:
PTG can be synthesized via several different methods. One of the most widely used methods involves the reaction of 4,6-O-benzylidene-1-thio-beta-D-glucose with phenylmagnesium bromide in dry ether. Afterward, the product is then extracted and purified. The compound can be further characterized using techniques such as nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and X-ray diffraction.
Analytical Methods:
Several analytical techniques have been used to detect and quantify PTG in scientific experiments. These include high-performance liquid chromatography (HPLC), gas chromatography-mass spectrometry (GC-MS), and liquid chromatography-mass spectrometry (LC-MS).
Biological Properties:
PTG has shown promising results as an antitumor and anti-inflammatory agent in various in vitro and in vivo studies. It has been shown to inhibit the growth of cancer cells and promote apoptosis through the activation of caspases. Additionally, it has been shown to reduce the levels of pro-inflammatory cytokines, such as TNF-? and IL-6, in animal models.
Toxicity and Safety in Scientific Experiments:
There are limited studies on the toxicity and safety of PTG in humans. However, in animal studies, no significant toxic effects have been observed at doses up to 1000mg/kg. However, further studies are required to determine its long-term effects and safety in humans.
Applications in Scientific Experiments:
PTG has potential applications in various fields of research and industry due to its unique properties. It has shown great promise as an antitumor and anti-inflammatory agent, making it a potential candidate for cancer treatment and other inflammatory diseases.
Current State of Research:
There has been some research on PTG in recent years, with several studies investigating its potential therapeutic effects. However, the majority of the research has been mainly focused on its biological properties and applications in cancer and inflammation.
Potential Implications in Various Fields of Research and Industry:
PTG has potential implications in various fields of research and industry, starting from pharmaceuticals to agriculture. Its antitumor and anti-inflammatory properties make it a potential candidate for developing new anticancer and anti-inflammatory agents. Moreover, its chemical properties could also make it a useful tool in the field of Chemical Biology, and other fields for synthesizing or manipulating related molecules.
Limitations and Future Directions:
Though PTG has demonstrated promising results in various scientific experiments, more research is needed to fully explore its potential applications. Several future directions can be considered, comprising the identification of more potential drug targets, exploration of suitable drug delivery methods, improving bioavailability of the compound, developing related analogs with even greater therapeutic potency, and research the industrial implications. Additionally, the compound’s potential toxicity and safety implications need to be evaluated more closely.
In conclusion, PTG is a chemical compound that has received attention in the biomedical field due to its antitumor and anti-inflammatory properties. The compound’s physical and chemical properties, as well as its applications, toxicity and safety, and future studies, have been analyzed. The present work highlights the potential of PTG in various fields of research and industry and provides useful information for further scientific research.
CAS Number | 71676-30-7 |
Product Name | Phenyl4,6-O-benzylidene-1-thio-beta-D-glucopyranoside |
IUPAC Name | (4aR,6S,7R,8R,8aS)-2-phenyl-6-phenylsulfanyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol |
Molecular Formula | C19H20O5S |
Molecular Weight | 360.42 g/mol |
InChI | InChI=1S/C19H20O5S/c20-15-16(21)19(25-13-9-5-2-6-10-13)23-14-11-22-18(24-17(14)15)12-7-3-1-4-8-12/h1-10,14-21H,11H2/t14-,15-,16-,17-,18?,19+/m1/s1 |
InChI Key | BDNIQCYVYFGHSI-LELVVPQVSA-N |
SMILES | C1C2C(C(C(C(O2)SC3=CC=CC=C3)O)O)OC(O1)C4=CC=CC=C4 |
Canonical SMILES | C1C2C(C(C(C(O2)SC3=CC=CC=C3)O)O)OC(O1)C4=CC=CC=C4 |
Isomeric SMILES | C1[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)SC3=CC=CC=C3)O)O)OC(O1)C4=CC=CC=C4 |
Size | 1 G, 100 MG, 5 G, Other |
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