Compound Information
|
ID |
112 |
TrivialName |
Gypenoside CXIV |
Type |
PPD |
MF |
C₄₈H₈₂O₂₀ |
MolecularWeight |
979.164 |
IUPACName |
NT |
m/z |
NT |
Retention Time |
NT |
CCS |
NT |
Adducts |
NT |
Isomeric SMILES |
C[C@@]12C(CC[C@]3(C)C2C[C@@H](O)C4[C@@]3(C)CC[C@@H]4[C@@](CCC(O)C(C)=C)(C)O[C@H]5[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O5)C(C)(C)[C@@H](O[C@H]6[C@H](O[C@H]7[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O7)[C@@H](O)[C@H](O)[C@@H](CO)O6)[C@@H](O)C1 |
Canonical SMILES |
C=C(C)C(O)CCC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC2(C)C1C(O)CC1C3(C)CC(O)C(OC4OC(CO)C(O)C(O)C4OC4OC(CO)C(O)C(O)C4O)C(C)(C)C3CCC12C |
Source |
Other |
Functions |
alleviates neuroinflammation and blood brain barrier |
Year |
2021 |
References |
Lou et al. (2021)
|
Structure |
|