| Name |
Hebevinoside IX 6-3-O-p-D-Xylopyranoside |
| Formula |
C35H58O7 |
| Mw |
590.41825421 |
| CAS RN |
101365-11-1 |
| C_ID |
C00023924
, 
|
| InChIKey |
QQKQWCLXOKWADM-UTKYIECRNA-N |
| InChICode |
InChI=1S/C35H58O7/c1-19(2)10-9-11-20(3)27-24(37)17-35(8)30-23(36)16-22-21(33(30,6)14-15-34(27,35)7)12-13-26(32(22,4)5)42-31-29(40)28(39)25(38)18-41-31/h10,16,20-21,23-31,36-40H,9,11-15,17-18H2,1-8H3/t20-,21+,23-,24-,25+,26-,27+,28+,29+,30+,31+,33-,34-,35-/m0/s1 |
| SMILES |
CC(C)=CCCC(C)C1[C@@H](O)CC2(C)C3[C@@H](O)C=C4C(CC[C@H](O[C@H]5OC[C@@H](O)[C@@H](O)C5O)C4(C)C)[C@]3(C)CCC12C |
| Start Substs in Alk. Biosynthesis (Prediction) |
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| Organism |
| Kingdom |
Family |
Species |
Reference |
| Fungi | Hymenogastraceae | Hebeloma vinosphyllum | Ref. |
|
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zoom in
| Organism | Hebeloma vinosphyllum | | Reference | Fujimoto,Chem.Pharm.Bull.,35,(1987),2254-2269 |
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