121748-11-6

Basic information

• Product Name: threo-1-C-Syringylglycerol
• Synonyms: threo-1-C-Syringylglycerol
• CAS NO: 121748-11-6
• Molecular Formula: C₁₁H₁₆O₆
• Molecular Weight: 244.24
• Mol File: 121748-11-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: threo-1-C-Syringylglycerol(CAS DataBase Reference)
• NIST Chemistry Reference: threo-1-C-Syringylglycerol(121748-11-6)
• EPA Substance Registry System: threo-1-C-Syringylglycerol(121748-11-6)

Safety Data

• Hazardous Substances Data: 121748-11-6(Hazardous Substances Data)

Usage

Description

threo-1-C-Syringylglycerol is a chemical constituent derived from Kandelia candel, a mangrove plant species. It is known for its potential inhibitory effects on pro-inflammatory cytokines production, particularly in LPS-stimulated bone marrow-derived dendritic cells (BMDCs). threo-1-C-Syringylglycerol has garnered interest due to its possible applications in various industries, including pharmaceutical and healthcare.

Uses

Used in Pharmaceutical and Healthcare Industry:
threo-1-C-Syringylglycerol is used as an anti-inflammatory agent for its potential to inhibit the production of pro-inflammatory cytokines in LPS-stimulated bone marrow-derived dendritic cells (BMDCs). This application is significant as it may contribute to the development of novel treatments for inflammatory diseases and conditions.
Additionally, threo-1-C-Syringylglycerol's potential to modulate immune responses could make it a valuable compound in the development of immunomodulatory therapies, further expanding its use in the pharmaceutical and healthcare industry.

Upstream product

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Relevant articles and documents

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.