strictinin
glucopyranose, cyclic 4,6-(4,4',5,5',6,6'-hexahydroxydiphenate) 1-gallate, beta-D-
 
Notes:
None found
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CAS Number: 517-46-4Picture of molecule3D/inchi
Nikkaji Web: J393.172B
XlogP3-AA: 0.10 (est)
Molecular Weight: 634.45794000
Formula: C27 H22 O18
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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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)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Nacalai USA
For experimental / research use only.
Strictinin
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Safety Information:
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
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.
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Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 73330
National Institute of Allergy and Infectious Diseases: Data
Chemidplus: 0000517464
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References:
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 73330
Pubchem (sid): 135030793
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEMBL: View
HMDB (The Human Metabolome Database): Search
FooDB: FDB018806
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 clove leaf
Search Trop  Picture
 guava leaf
Search Trop  Picture
 pomegranate leaf
Search Trop  Picture
 tea leaf
Search Trop  Picture
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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-
Synonyms   Articles   Notes   Search   Top
Articles:
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.
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