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hinokiflavone
6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-phenoxy]-5,7-dihydroxy-2-(4-hydroxy-phenyl)-chromen-4-one

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Name:6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
CAS Number: 19202-36-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:242-877-4
FDA UNII: Search
Nikkaji Web:J13.600J
MDL:MFCD00017455
XlogP3:4.40 (est)
Molecular Weight:538.46546000
Formula:C30 H18 O10
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: 841.00 to 842.00 °C. @ 760.00 mm Hg (est)
Flash Point: 545.00 °F. TCC ( 284.80 °C. ) (est)
logP (o/w): 5.528 (est)
Soluble in:
 water, 0.03816 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.
Hinokiflavone 98%
BOC Sciences
For experimental / research use only.
Hinokiflavone 0.97
Odor: characteristic
Use: Hinokiflavone isolated from the leaves of Platycladus orientalis. It has inhibition of MMP-9. significant cytotoxicity
Carbosynth
For experimental / research use only.
Hinokiflavone
Coompo
For experimental / research use only.
Hinokiflavone from Plants ≥97%
ExtraSynthese
For experimental / research use only.
Hinokiflavone (HPLC) ≥90%
 
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 hinokiflavone usage levels up to:
 not for fragrance use.
 
Recommendation for hinokiflavone 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 :5281627
National Institute of Allergy and Infectious Diseases:Data
6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
Chemidplus:0019202369
 
References:
 6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5281627
Pubchem (sid):135259754
 
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):C10057
HMDB (The Human Metabolome Database):Search
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cupressus torulosa cone
Search Trop Picture
 juniper
Search Trop Picture
 rhus retinorrhoea leaf
Search Trop Picture
 rhus succedanea
Search Trop Picture
 sugi
Search Trop Picture
 
Synonyms:
4H-1-benzopyran-4-one, 6-[4-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-
4',6''-biapigenin
4',6''-O-biapigenin
6-(4-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-phenoxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone
6-(4-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone
6-[4-(5,7-dihydroxy-4-oxo-4H-1-benzopyran-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone
6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-phenoxy]-5,7-dihydroxy-2-(4-hydroxy-phenyl)-chromen-4-one
6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one
 

Articles:

PubMed:Study of the hepatoprotective effect of Juniperus phoenicea constituents.
PubMed:[Simultaneous determination of selaginellins and biflavones in Selaginella tamariscina and S. pulvinata by HPLC].
PubMed:Isolation and cytotoxic activity of selaginellin derivatives and biflavonoids from Selaginella tamariscina.
PubMed:Selaginellin A and B, two novel natural pigments isolated from Selaginella tamariscina.
PubMed:Structurally unique biflavonoids from Selaginella chrysocaulos and Selaginella bryopteris.
PubMed:A new glucoside from Selaginella sinensis.
PubMed:Biflavones from Chamaecyparis obtusa.
PubMed:Antifungal biflavones from Cupressocyparis leylandii.
PubMed:In vitro anti-HIV activity of biflavonoids isolated from Rhus succedanea and Garcinia multiflora.
PubMed:[Chemical constitutents of Podocarpus imbricatus BI. (II)].
PubMed:Hinokiflavone, a cytotoxic principle from Rhus succedanea and the cytotoxicity of the related biflavonoids.
PubMed:Flavonoids in the leaves of Juniperus drupacea.
PubMed:Cryptomerin A and B, hinokiflavone methyl ethers from the leaves of Cryptomeria japonica.
PubMed:Discovery of potent inhibitor for matrix metalloproteinase-9 by pharmacophore based modeling and dynamics simulation studies.
PubMed:Study of the hepatoprotective effect of Juniperus phoenicea constituents.
PubMed:[Simultaneous determination of selaginellins and biflavones in Selaginella tamariscina and S. pulvinata by HPLC].
PubMed:Isolation and cytotoxic activity of selaginellin derivatives and biflavonoids from Selaginella tamariscina.
PubMed:Structural characterization and identification of biflavones in Selaginella tamariscina by liquid chromatography-diode-array detection/electrospray ionization tandem mass spectrometry.
PubMed:Selaginellin A and B, two novel natural pigments isolated from Selaginella tamariscina.
PubMed:Biflavones from Chamaecyparis obtusa.
PubMed:Biflavonoids from Cycas beddomei.
PubMed:Antifungal biflavones from Cupressocyparis leylandii.
PubMed:Antiviral activities of biflavonoids.
PubMed:[Chemical constitutents of Podocarpus imbricatus BI. (II)].
 
Notes:
from rhus succedanea.
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