|
Compound Information
|
| ID |
177 |
| TrivialName |
6-acetyl ginsenoside Rg3 |
| Type |
PPT |
| MF |
C₅₀H₈₄O₂₀ |
| MolecularWeight |
1005.202 |
| IUPACName |
NT |
| m/z |
NT |
| Retention Time |
NT |
| CCS |
NT |
| Adducts |
NT |
| Isomeric SMILES |
CC1(C)[C@@H](O[H])CC[C@@]2(C)C1[C@@H](O[C@H]3[C@H](O)[C@@H](O)[C@H](O[C@H]4[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O4)[C@@H](CO)O3)C[C@]5(C)C2C[C@@H](O[H])C6[C@@]5(C)CCC6[C@@](C)(O[C@H]7[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(C)=O)O7)CC/C=C(C)/C |
| Canonical SMILES |
CC(=O)OCC1OC(OC(C)(CCC=C(C)C)C2CCC3(C)C2C(O)CC2C4(C)CCC(O)C(C)(C)C4C(OC4OC(CO)C(OC5OC(CO)C(O)C(O)C5O)C(O)C4O)CC23C)C(O)C(O)C1O |
| Source |
PG |
| Functions |
Hydroxyl radical scavenging activity, antibacterial, anticancer |
| Year |
2015 |
| References |
Lee et al. (2015)
|
| Structure |
|
