ChemicalBook--->CAS DataBase List--->130608-11-6

130608-11-6

130608-11-6 Structure

130608-11-6 Structure
IdentificationBack Directory
[Name]

Benzo[6,7]cyclohepta[1,2,3-cd]benzofuran-4,6,8,10-tetrol,1,6,7,11b-tetrahydro-1,7-bis(4-hydroxyphenyl)-, (1S,6R,7S,11bS)-
[CAS]

130608-11-6
[Synonyms]

Benzo[6,7]cyclohepta[1,2,3-cd]benzofuran-4,6,8,10-tetrol,1,6,7,11b-tetrahydro-1,7-bis(4-hydroxyphenyl)-, (1S,6R,7S,11bS)-
[Molecular Formula]

C28H22O7
[MOL File]

130608-11-6.mol
[Molecular Weight]

470.47
Chemical PropertiesBack Directory
[InChIKey]

LHUHHURKGTUZHU-TYDIULBZNA-N
[SMILES]

O1C2=CC(O)=CC3[C@H](O)[C@@H](C4=CC=C(O)C=C4)C4=C(O)C=C(O)C=C4[C@@]([H])(C2=3)[C@H]1C1=CC=C(O)C=C1 |&1:7,9,25,28,r|
Hazard InformationBack Directory
[Description]

Ampelopsin reduces the migration and invasion of ovarian cancer cells via inhibition of epithelial-to-mesenchymal transition.
[Uses]

Ampelopsin A is a antifungal agent and can be isolated from the Vitis vinifera canes. Ampelopsin A shows neuroprotective effects[1][2].
[References]

[1] Schnee S, et al. Vitis vinifera canes, a new source of antifungal compounds against Plasmopara viticola, Erysiphe necator, and Botrytis cinerea. J Agric Food Chem. 2013;61(23):5459-5467. DOI:10.1021/jf4010252
[2] Hong Y, et al. Central Administration of Ampelopsin A Isolated from Vitis vinifera Ameliorates Cognitive and Memory Function in a Scopolamine-Induced Dementia Model. Antioxidants (Basel). 2021;10(6):835. Published 2021 May 24. DOI:10.3390/antiox10060835
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