norartocarpetin
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
Identification
| Name | norartocarpetin |
| CAS Number | 520-30-9 |
| FDA UNII | Search |
| Molecular Formula | C15 H10 O6 |
| Molecular Weight | 286.23990000 |
| Nikkaji Number | J11.597E |
| XlogP3 | 1.40 (est) |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 536.8 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 norartocarpetin usage levels up to | not for fragrance use. |
| Recommendation for norartocarpetin flavor usage levels up to | not for flavor use. |
No supplier data available
Potential Uses
Natural Occurrence
Synonyms
4H-1-
benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-
2-(2,4-
dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
2-(2,4-
dihydroxyphenyl)-5,7-dihydroxychromen-4-one
PubMed:
Investigating the inhibitory activity and mechanism differences between norartocarpetin and luteolin for tyrosinase: A combinatory kinetic study and computational simulation analysis.
PubMed:
Tyrosinase inhibitory activity of flavonoids from Artocarpus heterophyllous.
PubMed:
A phenylacetaldehyde-flavonoid adduct, 8-C-(E-phenylethenyl)-norartocarpetin, exhibits intrinsic apoptosis and MAPK pathways-related anticancer potential on HepG2, SMMC-7721 and QGY-7703.
PubMed:
Chemical constituents derived from Artocarpus xanthocarpus as inhibitors of melanin biosynthesis.
PubMed:
Preparation, characterization, and preliminary antibrowning evaluations of norartocarpetin microemulsions.
PubMed:
A new antioxidant stilbene and other constituents from the stem bark of Morus nigra L.
PubMed:
Norartocarpetin from a folk medicine Artocarpus communis plays a melanogenesis inhibitor without cytotoxicity in B16F10 cell and skin irritation in mice.
PubMed:
[Chemical constituents from cell cultures of Morus alba].
PubMed:
Prenylated flavonoids from Artocarpus altilis: antioxidant activities and inhibitory effects on melanin production.
PubMed:
Flavonoids and triterpenes from the leaves of Artocarpus fulvicortex.
PubMed:
Phosphodiesterase I-inhibiting Diels-Alder adducts from the leaves of Morus mesozygia.
PubMed:
Artocarpus plants as a potential source of skin whitening agents.
PubMed:
[Flavonoids from the leaves of Morus alba L].
PubMed:
Stilbenes and flavonoids from Artocarpus nitidus subsp. lingnanensis.
PubMed:
Three new compounds from Morus nigra L.
PubMed:
Chemical components and tyrosinase inhibitors from the twigs of Artocarpus heterophyllus.
PubMed:
Isolation of tyrosinase inhibitors from Artocarpus heterophyllus and use of its extract as antibrowning agent.
PubMed:
Inhibitory effects on mushroom tyrosinase by flavones from the stem barks of Morus lhou (S.) Koidz.
PubMed:
Anti-inflammatory effects of phenolic compounds isolated from the fruits of Artocarpus heterophyllus.
PubMed:
Antiherpetic flavones from the heartwood of Artocarpus gomezianus.
PubMed:
Cytotoxic flavonoids and new chromenes from Ficus formosana f. formosana.
PubMed:
Constituents of the bark and twigs of Artocarpus dadah with cyclooxygenase inhibitory activity.
PubMed:
Tyrosinase inhibitors from Artocarpus gomezianus.