SAPOPYROSIDE

Structure

2D structure of SAPOPYROSIDE
2D structure
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3D model

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

Names and identifiers

Name

SAPOPYROSIDE

IUPAC name

(3R,4S,5R,6R)-2-(((2S,3S,4S)-3-acetoxy-2-methyl-3,4-dihydro-2H-pyran-4-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

SMILES

[C@@H]1(C=CO[C@H]([C@@H]1OC(C)=O)C)OC2[C@@H]([C@H]([C@@H]([C@@H](COC(C)=O)O2)OC(C)=O)OC(C)=O)OC(C)=O

General information

Molecular formula

C22H30O13

Molecular weight

502.47 g/mol

Monoisotopic mass

502.1686 Da

Classification

Pathway:
Superclass:
Class:
-
Glycoside:
Yes

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

Plants with the compound

Plant Plant part Amount Reference
Saponaria officinalis L. flower -
Plouvier, V., Martin, M.T., Brouard, J.P. (1986). Two pyran type glycosides from Saponaria and Dianthus. Phytochemistry, 25(2), 546-548 doi:10.1016/s0031-9422(00)85525-9
Saponaria officinalis L. leaf -
Plouvier, V., Martin, M.T., Brouard, J.P. (1986). Two pyran type glycosides from Saponaria and Dianthus. Phytochemistry, 25(2), 546-548 doi:10.1016/s0031-9422(00)85525-9
Saponaria officinalis L. root -
Plouvier, V., Martin, M.T., Brouard, J.P. (1986). Two pyran type glycosides from Saponaria and Dianthus. Phytochemistry, 25(2), 546-548 doi:10.1016/s0031-9422(00)85525-9
Saponaria officinalis L. stem -
Plouvier, V., Martin, M.T., Brouard, J.P. (1986). Two pyran type glycosides from Saponaria and Dianthus. Phytochemistry, 25(2), 546-548 doi:10.1016/s0031-9422(00)85525-9