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byakangelicol
9-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4-methoxyfuro[3,2-g]chromen-7-one

Supplier Sponsors

Name:9-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4-methoxyfuro[3,2-g]chromen-7-one
CAS Number: 26091-79-2Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J16.924B
MDL:MFCD06796689
XlogP3-AA:2.60 (est)
Molecular Weight:316.30972000
Formula:C17 H16 O6
BioActivity Summary:listing
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
Boiling Point: 503.00 to 504.00 °C. @ 760.00 mm Hg (est)
Flash Point: 497.00 °F. TCC ( 258.30 °C. ) (est)
logP (o/w): 1.564 (est)
Soluble in:
 alcohol
 water, 55.77 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
Biacangelicol; Byakangelicol 98%
BOC Sciences
For experimental / research use only.
7H-Furo[3,2-g][1]benzopyran-7-one,9-[[(2R)-3,3-dimethyl-2-oxiranyl]methoxy]-4-methoxy-
Carbosynth
For experimental / research use only.
Byakangelicol
 
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 byakangelicol usage levels up to:
 not for fragrance use.
 
Recommendation for byakangelicol 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 :3055167
National Institute of Allergy and Infectious Diseases:Data
9-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4-methoxyfuro[3,2-g]chromen-7-one
Chemidplus:0026091792
 
References:
 9-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4-methoxyfuro[3,2-g]chromen-7-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):3055167
Pubchem (sid):135151725
 
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):C16925
HMDB (The Human Metabolome Database):Search
FooDB:FDB005024
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
 lemon fruit oil
Search Trop Picture
 lemon oil
Search Trop Picture
 
Synonyms:
(R)-9-((3,3-dimethyl-2-oxiranyl)methoxy)-4-methoxyfuro(3,2-g)chromen-7-one
9-[[(2R)-3,3-dimethyloxiran-2-yl]methoxy]-4-methoxyfuro[3,2-g]chromen-7-one
7H-furo(3,2-g)(1)benzopyran-7-one, 9-((3,3-dimethyloxiranyl)methoxy)-4-methoxy-, (R)-
 

Articles:

PubMed:Biotransformation products of phellopterin by rat liver microsomes and the inhibition on NO production in LPS-activated RAW264.7 cells.
PubMed:Multidimensional liquid chromatography for the determination of chiral coumarins and furocoumarins in Citrus essential oils.
PubMed:Chemometric classification of morphologically similar Umbelliferae medicinal herbs by DART-TOF-MS fingerprint.
PubMed:Inhibitory effects of furanocoumarin derivatives in Kampo extract medicines on P-glycoprotein at the blood-brain barrier.
PubMed:Antigenotoxic activity of naturally occurring furanocoumarins.
PubMed:Simultaneous quantification of 17 constituents from Yuanhu Zhitong tablet using rapid resolution liquid chromatography coupled with a triple quadrupole electrospray tandem mass spectrometry.
PubMed:Rapid identification of furanocoumarins in Angelica dahurica using the online LC-MMR-MS and their nitric oxide inhibitory activity in RAW 264.7 cells.
PubMed:Furanocoumarin derivatives in Kampo extract medicines inhibit cytochrome P450 3A4 and P-glycoprotein.
PubMed:beta-secretase inhibitory effects of furanocoumarins from the root of Angelica dahurica.
PubMed:Simultaneous determination of five coumarins in Angelicae dahuricae Radix by HPLC/UV and LC-ESI-MS/MS.
PubMed:Antiproliferative effect of furanocoumarins from the root of Angelica dahurica on cultured human tumor cell lines.
PubMed:Antioxidative activity of furanocoumarins isolated from Angelicae dahuricae.
PubMed:HPLC-NMR/HPLC-MS analysis of the bark extract of Stauranthus perforatus.
PubMed:Byakangelicol, isolated from Angelica dahurica, inhibits both the activity and induction of cyclooxygenase-2 in human pulmonary epithelial cells.
PubMed:Furocoumarins from Angelica dahurica with hepatoprotective activity on tacrine-induced cytotoxicity in Hep G2 cells.
PubMed:Inducible nitric oxide synthase inhibitors of Chinese herbs. Part 2: naturally occurring furanocoumarins.
PubMed:Minor furocoumarins of Murraya koenigii.
PubMed:Characterisation of the furanocoumarin phellopterin as a rat brain benzodiazepine receptor partial agonist in vitro.
 
Notes:
None found
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