|
Compound Information
|
| ID |
85 |
| TrivialName |
ginsenoside Rs11 |
| Type |
PPD |
| MF |
C₅₅H₉₂O₂₃ |
| MolecularWeight |
1121.318 |
| IUPACName |
NT |
| m/z |
1165.6011 |
| Retention Time |
43.1 |
| CCS |
344.66 |
| Adducts |
NT |
| Isomeric SMILES |
CC1(C)[C@@H](O[C@H]2[C@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(C)=O)O3)[C@@H](O)[C@H](O)[C@@H](CO)O2)CC[C@@]4(C)C1CC[C@]5(C)C4C[C@@H](O)C6[C@@]5(C)CCC6[C@@](C)(O[C@H]7[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@H]8[C@H](O)[C@@H](O)[C@H](CO)O8)O7)CC/C=C(C)/C |
| Canonical SMILES |
CC(=O)OCC1OC(OC2C(OC3CCC4(C)C(CCC5(C)C4CC(O)C4C(C(C)(CCC=C(C)C)OC6OC(COC7OC(CO)C(O)C7O)C(O)C(O)C6O)CCC45C)C3(C)C)OC(CO)C(O)C2O)C(O)C(O)C1O |
| Source |
PG |
| Functions |
Hydroxyl radical scavenging activity, antibacterial, anticancer, antioxidant
|
| Year |
2015 |
| References |
Lee et al. (2015)
|
| Structure |
|
