EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

gardenin B

Supplier Sponsors

CAS Number: 2798-20-1Picture of molecule3D/inchi
FDA UNII: 313E89KN5E
Nikkaji Web:J94.492K
XlogP3-AA:3.30 (est)
Molecular Weight:358.34686000
Formula:C19 H18 O7
NMR Predictor:Predict (works with chrome, Edge 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
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 11.46 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Gardenin B 98%
BOC Sciences
For experimental / research use only.
Gardenin B >98%
 
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
 
Safety in Use Information:
Category:
natural substances and extractives
Recommendation for gardenin B usage levels up to:
 not for fragrance use.
 
Recommendation for gardenin B flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :96539
National Institute of Allergy and Infectious Diseases:Data
5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one
Chemidplus:0002798201
 
References:
 5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):96539
Pubchem (cas):2798-20-1
 
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
CHEBI:View
CHEMBL:View
KEGG (GenomeNet):C15109
HMDB (The Human Metabolome Database):Search
FooDB:FDB002752
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 satureja montana
Search Trop Picture
 
Synonyms:
4H-1-benzopyran-4-one, 5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-
5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
5-hydroxy-6,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one
 

Articles:

PubMed:Characterization of bioactive constituents from the gum resin of Gardenia lucida and its pharmacological potential.
PubMed:Gardenin B-induced cell death in human leukemia cells involves multiple caspases but is independent of the generation of reactive oxygen species.
PubMed:Simultaneous Quantification of Five Bioactive Flavonoids in High Altitude Plant Actinocarya tibetica by LC-ESI-MS/MS.
PubMed:Identification of a unique 2-oxoglutarate-dependent flavone 7-O-demethylase completes the elucidation of the lipophilic flavone network in basil.
PubMed:5-demethyltangeretin inhibits human nonsmall cell lung cancer cell growth by inducing G2/M cell cycle arrest and apoptosis.
PubMed:Effect of a labile methyl donor on the transformation of 5-demethyltangeretin and the related implication on bioactivity.
PubMed:Characterization of two candidate flavone 8-O-methyltransferases suggests the existence of two potential routes to nevadensin in sweet basil.
PubMed:Biological activity of secondary metabolites from Peltostigma guatemalense.
PubMed:Distribution of 8-oxygenated leaf-surface flavones in the genus Ocimum.
PubMed:A distinctive flavonoid chemistry for the anomalous genus Biebersteinia.
 
Notes:
None found
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