Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H22O12 |
| Molecular Weight | 466.3922 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 7 / 7 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@@H](O[C@@H]2[C@H](OC3=CC(O)=CC(O)=C3C2=O)C4=CC=C(O)C(O)=C4)[C@H](O)[C@@H](O)[C@@H]1O
InChI
InChIKey=FVQOMEDMFUMIMO-UTZHSPHRSA-N
InChI=1S/C21H22O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-27,29-30H,6H2/t13-,15-,17+,18-,19-,20+,21+/m1/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Preparative purification of five bioactive components from Agrimonia pilosa Ledeb by high-speed counter-current chromatography. | 2012-08 |
|
| PREPARATIVE SEPARATION OF AXIFOLIN-3-GLUCOSIDE, HYPEROSIDE AND AMYGDALIN FROM PLANT EXTRACTS BY HIGH-SPEED COUNTERCURRENT CHROMATOGRAPHY. | 2009-01-01 |
|
| [Studies on the monomer flavonoides of the plants of coniferae. 3. Distribution of taxifolin-3-glucoside in the leaves of coniferae]. | 1967-01 |
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SUBSTANCE RECORD
