1464-44-4
Chemical Structure
Phenyl β-D-glucopyranoside
- CAS No.: 1464-44-4
- Formula:C12H16O6
- Molecular Weight:256.25
IUPAC Name: (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-phenoxytetrahydro-2H-pyran-3,4,5-triol
InChIKey: NEZJDVYDSZTRFS-RMPHRYRLSA-N
SMILES: O[C@H]([C@H]([C@@H]([C@H](O1)CO)O)O)[C@@H]1OC2=CC=CC=C2
Biological Activity: Phenyl β-D-glucopyranoside is a component isolated from Phellodendron amurense, which has anti-inflammatory and anti-tumor activities. Phenyl β-D-glucopyranoside inhibits nitric oxide (NO) production, and the expression of iNOS and COX-2. Phenyl β-D-glucopyranoside also inhibits the nuclear translocation of NF-κB. Phenyl β-D-glucopyranoside inhibits the expression of pro-inflammatory cytokines and related genes[1][2].
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Phenyl β-D-glucopyranoside | 99.85% | Phenyl β-D-glucopyranoside is a component isolated from Phellodendron amurense, which has anti-inflammatory and anti-tumor activities. Phenyl β-D-glucopyranoside inhibits nitric oxide (NO) production, and the expression of iNOS and COX-2. Phenyl β-D-glucopyranoside also inhibits the nuclear translocation of NF-κB. Phenyl β-D-glucopyranoside inhibits the expression of pro-inflammatory cytokines and related genes. | ||||||||||||||||||||
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Phenyl β-D-glucopyranoside (Standard) | ≥98% | Phenyl β-D-glucopyranoside (Standard) is the analytical standard of Phenyl β-D-glucopyranoside (HY-W011849). This product is intended for research and analytical applications. Phenyl β-D-glucopyranoside is a component isolated from Phellodendron amurense, which has anti-inflammatory and anti-tumor activities. Phenyl β-D-glucopyranoside inhibits nitric oxide (NO) production, and the expression of iNOS and COX-2. Phenyl β-D-glucopyranoside also inhibits the nuclear translocation of NF-κB. Phenyl β-D-glucopyranoside inhibits the expression of pro-inflammatory cytokines and related genes. | ||||||||||||||||||||
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References
- [1]. Hwang SJ, et al. Phenyl-β-D-Glucopyranoside Exhibits Anti-inflammatory Activity in Lipopolysaccharide-Activated RAW 264.7 Cells. Inflammation. 2015;38(3):1071-9. [Content Brief]
- [2]. Usabiaga I, et al. Phenyl-β-D-glucopyranoside and Phenyl-β-D-galactopyranoside Dimers: Small Structural Differences but Very Different Interactions[J]. Frontiers in Physics, 2018, 6: 3.
