| Name |
(10S)-8,9-Dihydro-10-(2,4-dihydroxyphenyl)-8-(3,4-dihydroxyphenyl)-9-hydroxy-10H-pyrano[2,3-h]catechin |
| Formula |
C30H26O11 |
| Mw |
562.14751167 |
| CAS RN |
102258-25-3 |
| C_ID |
C00008948
, 
|
| InChIKey |
AMVCEZYBLCNDSF-HTKBHMLYNA-N |
| InChICode |
InChI=1S/C30H26O11/c31-14-3-4-15(19(34)9-14)25-26-24(40-29(27(25)39)13-2-6-18(33)22(37)8-13)11-20(35)16-10-23(38)28(41-30(16)26)12-1-5-17(32)21(36)7-12/h1-9,11,23,25,27-29,31-39H,10H2/t23-,25-,27+,28+,29+/m0/s1 |
| SMILES |
c1(c2c(c3c(c1)O[C@@H]([C@@H]([C@H]3c1ccc(cc1O)O)O)c1ccc(c(c1)O)O)O[C@@H]([C@H](C2)O)c1cc(c(cc1)O)O)O |
| Start Substs in Alk. Biosynthesis (Prediction) |
|
| Organism |
| Kingdom |
Family |
Species |
Reference |
| Plantae | Fabaceae | Baikiaea plurijuga | Ref. |
| Plantae | Fabaceae | Guibourtia coleosperma  | Ref. |
|
|
zoom in
| Organism | Guibourtia coleosperma |
|---|
| Reference | Harborne, The Handbook of Natural Flavonoids, 2, (1999), 355,Flavans and proanthocyanidins
Steenkamp,J.Chem.Soc.Chem.Commun,(1985),1678
Steynberg,J.Chem.Soc.Perkin Trans.,1,(1988),3323 |
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