strictinin
glucopyranose, cyclic 4,6-(4,4',5,5',6,6'-hexahydroxydiphenate) 1-gallate, beta-D-
Identification
| Name | strictinin |
| CAS Number | 517-46-4 |
| FDA UNII | Search |
| Molecular Formula | C27 H22 O18 |
| Molecular Weight | 634.45794000 |
| Nikkaji Number | J393.172B |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 1280.80 °C. @ 760.00 mm Hg (est) |
| Flash Point | 786.00 °F. TCC ( 418.80 °C. ) (est) |
| logP (o/w) | 2.670 (est) |
| Soluble in | water, 427.5 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for strictinin usage levels up to | not for fragrance use. |
| Recommendation for strictinin flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
glucopyranose, cyclic 4,6-(4,4',5,5',6,6'-hexahydroxydiphenate) 1-gallate, beta-D-
glucopyranose, cyclic 4,6-(4,4',5,5',6,6'-hexahydroxydiphenate) 1-gallate, β-D-
PubMed:
Identification of Ellagitannins and Flavonoids from Eugenia brasilienses Lam. (Grumixama) by HPLC-ESI-MS/MS.
PubMed:
In situ label-free visualization of orally dosed strictinin within mouse kidney by MALDI-MS imaging.
PubMed:
IL-4 receptor α in non-lipid rafts is the target molecule of strictinin in inhibiting STAT6 activation.
PubMed:
Tea polyphenols as novel and potent inhibitory substances against renin activity.
PubMed:
Phenolic antioxidants from Rosa soulieana flowers.
PubMed:
An overview on antidiabetic medicinal plants having insulin mimetic property.
PubMed:
High-yield total synthesis of (-)-strictinin through intramolecular coupling of gallates.
PubMed:
A non-targeted approach to chemical discrimination between green tea dietary supplements and green tea leaves by HPLC/MS.
PubMed:
Antiviral effect of strictinin on influenza virus replication.
PubMed:
Chemosystematics of tea trees based on tea leaf polyphenols as phenetic markers.
PubMed:
Identification of alpha-glucosidase inhibitors from a new fermented tea obtained by tea-rolling processing of loquat (Eriobotrya japonica) and green tea leaves.
PubMed:
Enhancement of phagocytic activity of macrophage-like cells by pyrogallol-type green tea polyphenols through caspase signaling pathways.
PubMed:
Identifications of inhibitors of IgE production by human lymphocytes isolated from 'Cha Chuukanbohon Nou 6' tea leaves.
PubMed:
Metabolomics analysis reveals the compositional differences of shade grown tea (Camellia sinensis L.).
PubMed:
Identification of a major polyphenol and polyphenolic composition in leaves of Camellia irrawadiensis.
PubMed:
Immunostimulating activity of a crude polysaccharide derived from green tea (Camellia sinensis) extract.
PubMed:
Simultaneous analysis of catechins, gallic acid, strictinin, and purine alkaloids in green tea by using catechol as an internal standard.
PubMed:
Determination of mechanism of flock sediment formation in tea beverages.
PubMed:
Strictinin as an efficient antioxidant in lipid peroxidation.
PubMed:
New cyanogenic and alkyl glycoside constituents from Phyllagathis rotundifolia.
PubMed:
Identification of an inhibitor for interleukin 4-induced epsilon germline transcription and antigen-specific IgE production in vivo.
PubMed:
Pelargoniins, new ellagitannins from Pelargonium reniforme.
PubMed:
Preparative separation of polyphenols from tea by high-speed countercurrent chromatography.
PubMed:
New hydrolyzable tannins, shephagenins A and B, from Shepherdia argentea as HIV-1 reverse transcriptase inhibitors.
PubMed:
Antitumor agents, 129. Tannins and related compounds as selective cytotoxic agents.