| Name |
Cytisoside
Trematin
8-beta-D-Glucopyranosyl-5,7-dihydroxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one |
| Formula |
C22H22O10 |
| Mw |
446.12129692 |
| CAS RN |
2326-34-3 |
| C_ID |
C00006130
, 
|
| InChIKey |
ADCCDGCXRFALSQ-PLAKOYNZNA-N |
| InChICode |
InChI=1S/C22H22O10/c1-30-10-4-2-9(3-5-10)14-7-13(26)16-11(24)6-12(25)17(21(16)31-14)22-20(29)19(28)18(27)15(8-23)32-22/h2-7,15,18-20,22-25,27-29H,8H2,1H3/t15-,18-,19+,20+,22+/m1/s1 |
| SMILES |
COc1ccc(-c2cc(=O)c3c(O)cc(O)c([C@@H]4OC(CO)[C@@H](O)[C@H](O)C4O)c3o2)cc1 |
| Start Substs in Alk. Biosynthesis (Prediction) |
|
| Organism |
| Kingdom |
Family |
Species |
Reference |
| Plantae | Aytoniaceae | Reboulia hemisphaerica | Ref. |
| Plantae | Cannabaceae | Cannabis sativa  | Ref. |
| Plantae | Fabaceae | Cytisus laburnum | Ref. |
| Plantae | Fabaceae | Lupinus arboreus | Ref. |
|
|
zoom in
| Organism | Reboulia hemisphaerica |
|---|
| Reference | Harborne, The Handbook of Natural Flavonoids, 1, (1999), 549,C-glycosylflavones
Paris,C.R.Acad.Sci.Paris,245,(1957),443
Paris,C.R.Acad.Sci.Paris,252,(1957),1653 |
|---|
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