hinokiflavone
6-[4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)-phenoxy]-5,7-dihydroxy-2-(4-hydroxy-phenyl)-chromen-4-one
Identification
| Name | hinokiflavone |
| IUPAC | 6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)phenoxy]-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one |
| CAS Number | 19202-36-9 |
| EINECS | 242-877-4 |
| FDA UNII | Search |
| Molecular Formula | C30 H18 O10 |
| Molecular Weight | 538.46546000 |
| MDL Number | MFCD00017455 |
| Nikkaji Number | J13.600J |
| XlogP3 | 4.40 (est) |
Regulatory
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) |
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 hinokiflavone usage levels up to | not for fragrance use. |
| Recommendation for hinokiflavone flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
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
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)].