欢迎光临~北京凯森莱科技有限公司
语言选择: 中文版 ∷  英文版
  • 80154-34-3, 豆腐果苷, Helicid, CAS:80154-34-3
  • 80154-34-3, 豆腐果苷, Helicid, CAS:80154-34-3
80154-34-3, 豆腐果苷, Helicid, CAS:80154-34-380154-34-3, 豆腐果苷, Helicid, CAS:80154-34-3

80154-34-3, 豆腐果苷, Helicid, CAS:80154-34-3

80154-34-3, 豆腐果苷,
Helicid,
CAS:80154-34-3
C13H16O7 / 284.262
MFCD00210992

豆腐果苷, Helicid

4-Formylphenyl b-D-allopyranoside

4-Formylphenyl b-D-allopyranoside is a natural drug that has been shown to have biological properties. It has shown to inhibit the transcriptional regulation of genes via the matrix effect and p-hydroxybenzoic acid, which may be due to its ability to form stable complexes with DNA. The stability of these complexes may be due in part to their interaction with the surface methodology. 4-Formylphenyl b-D-allopyranoside has also been shown to increase locomotor activity in mice, as well as inducing secretion from gland cells in human serum.

Helicid, also known as helicobacter pylori urease inhibitor (HPUreI), is a compound that has attracted the attention of scientists due to its potential applications in various scientific and industrial fields. This paper provides an overview of the definition and background of helicid, its physical and chemical properties, synthesis and characterization, analytical methods, biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, and limitations and future directions.

Definition and Background:

Helicid is a urease inhibitor that was originally isolated from the leaves of cashew nut trees. It was identified as a potent inhibitor of the urease activity of Helicobacter pylori, a bacterium that causes gastric ulcers and stomach cancers. Helicid is a novel compound that has the potential to offer new insights into the mechanisms of bacterial pathogenesis and drug discovery.

Synthesis and Characterization:

Helicid can be synthesized from natural sources, such as cashew nut tree leaves, or chemically synthesized using various synthetic routes. The synthesis of helicid involves the formation of the compound's imidazole ring, which is critical for its urease inhibitory activity. Characterization of helicid can be done using various spectroscopic techniques, such as nuclear magnetic resonance (NMR), infrared (IR), and mass spectrometry (MS).

Analytical Methods:

Analytical methods, such as high-performance liquid chromatography (HPLC), gas chromatography (GC), and capillary electrophoresis (CE), are used to analyze the purity, stability, and degradation of helicid. These methods are also used to determine the pharmacokinetics and pharmacodynamics of helicid in vivo.

Biological Properties:

Helicid has been shown to be a potent inhibitor of Helicobacter pylori urease activity, which is critical for the survival and pathogenesis of this bacterium. Helicid has also been shown to have antibacterial activity against other pathogenic bacteria, such as Escherichia coli, Klebsiella pneumoniae, and Staphylococcus aureus. Helicid's antibacterial activity is due to its ability to disrupt bacterial cell walls and membranes.

Toxicity and Safety in Scientific Experiments:

Helicid has been shown to be safe in scientific experiments, with no adverse effects observed in animal studies. However, further studies are needed to determine the long-term effects of helicid on human health.

Applications in Scientific Experiments:

Helicid has potential applications in various scientific experiments, such as drug discovery and biotechnology. Helicid's inhibitory activity against Helicobacter pylori's urease activity makes it a promising target for the development of new antibiotics. Helicid can also be used as a tool in biotechnology to study the mechanisms of bacterial pathogenesis and disease.

Current State of Research:

Research on helicid is ongoing, with studies focusing on its antibacterial activity, mechanisms of action, and potential applications in drug discovery and biotechnology. Various synthetic routes for helicid synthesis are also being explored to improve its yield and purity.

Potential Implications in Various Fields of Research and Industry:

Helicid has potential implications in various fields of research and industry. In the medical field, helicid can be used in the development of new antibiotics to treat bacterial infections, especially those caused by Helicobacter pylori. In the biotechnology field, helicid can be used as a tool to study bacterial pathogenesis and disease. Helicid can also have applications in the food industry, as a preservative or antimicrobial agent in food packaging.

Limitations and Future Directions:

Despite its potential applications, the use of helicid is limited by its low solubility and stability in physiological conditions. Future research should focus on improving helicid's solubility and stability, as well as exploring new synthetic routes to improve its yield and purity. Other future directions include the development of new derivatives of helicid with improved antibacterial activity and the exploration of helicid's potential as a therapeutic agent for diseases such as cancer and Alzheimer's disease.

CAS Number80154-34-3
Product NameHelicid
IUPAC Name4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzaldehyde
Molecular FormulaC₁₃H₁₆O₇
Molecular Weight284.26 g/mol
InChIInChI=1S/C13H16O7/c14-5-7-1-3-8(4-2-7)19-13-12(18)11(17)10(16)9(6-15)20-13/h1-5,9-13,15-18H,6H2/t9-,10-,11-,12-,13-/m1/s1
InChI KeyBGOFCVIGEYGEOF-WJTVCTBASA-N
SMILESC1=CC(=CC=C1C=O)OC2C(C(C(C(O2)CO)O)O)O
SynonymsHelicide; Helicidum
Canonical SMILESC1=CC=C(C(=C1)C=O)OC2C(C(C(C(O2)CO)O)O)O
Isomeric SMILESC1=CC=C(C(=C1)C=O)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)CO)O)O)O


CAS No: 80154-34-3 Synonyms: 4-b-D-Allopyranosyloxy)benzaldehyde MDL No: MFCD00210992 Chemical Formula: C13H16O7 Molecular Weight: 284.26
References: 1. J. Proc. R.Soc. NSW., 1936, 70, p440

在线询价

用手机扫描二维码关闭
二维码