BRYOAMARIDE

Structure

2D structure of BRYOAMARIDE
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 44584115

Names and identifiers

Name

BRYOAMARIDE

IUPAC name

(8S,9R,10R,13R,14S,16R,17R)-17-((S)-2,6-dihydroxy-6-methyl-3-oxoheptan-2-yl)-16-hydroxy-4,4,9,13,14-pentamethyl-2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-7,8,9,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthrene-3,11(4H)-dione

SMILES

C[C@@]12C[C@H]([C@@H]([C@]1(CC(=O)[C@@]3([C@H]2CC=C4[C@H]3C=C(C(=O)C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)C)[C@@](C)(C(=O)CCC(C)(C)O)O)O

General information

Molecular formula

C36H54O12

Molecular weight

678.82 g/mol

Monoisotopic mass

678.3615 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
Yes

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Bryonia dioica Jacq. root -
Ripperger, H. (1976). Isolation and structure of cucurbitacins from Bryonia dioica. Tetrahedron, 32, 1567 doi:10.1002/chin.197646317
Bryonia dioica Jacq. root -
Ukiya, M., Akihisa, T., Yasukawa, K., Tokuda, H., Toriumi, M., Koike, K., Kimura, Y., Nikaido, T., Aoi, W., Nishino, H., Takido, M. (2002). Anti-inflammatory and anti-tumor-promoting effects of cucurbitane glycosides from the roots of Bryonia dioica. J Nat Prod, 65(2), 179-183 doi:10.1021/np010423u