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
[H][C@@]4(O[C@@H]1[C@H](OC2=C(C1=O)C(O)=CC(O)=C2)C3=CC(O)=C(O)C=C3)O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O
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 |
|---|---|---|
| [Studies on the monomer flavonoides of the plants of coniferae. 3. Distribution of taxifolin-3-glucoside in the leaves of coniferae]. | 1967 Jan |
|
| PREPARATIVE SEPARATION OF AXIFOLIN-3-GLUCOSIDE, HYPEROSIDE AND AMYGDALIN FROM PLANT EXTRACTS BY HIGH-SPEED COUNTERCURRENT CHROMATOGRAPHY. | 2009 Jan 1 |
|
| Preparative purification of five bioactive components from Agrimonia pilosa Ledeb by high-speed counter-current chromatography. | 2012 Aug |
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DTXSID80181740
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SUBSTANCE RECORD
