| Stereochemistry | ABSOLUTE |
| Molecular Formula | C27H24O18 |
| Molecular Weight | 636.4687 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O[C@@H]1[C@@H](COC(=O)C2=CC(O)=C(O)C(O)=C2)O[C@@H](OC(=O)C3=CC(O)=C(O)C(O)=C3)[C@H](O)[C@H]1OC(=O)C4=CC(O)=C(O)C(O)=C4
InChI
InChIKey=RNKMOGIPOMVCHO-SJMVAQJGSA-N
InChI=1S/C27H24O18/c28-11-1-8(2-12(29)18(11)34)24(39)42-7-17-21(37)23(44-25(40)9-3-13(30)19(35)14(31)4-9)22(38)27(43-17)45-26(41)10-5-15(32)20(36)16(33)6-10/h1-6,17,21-23,27-38H,7H2/t17-,21-,22-,23+,27+/m1/s1
1,3,6-tri-O-galloyl-β-D-glucose was isolated from Euphorbia lunulata Bge and from the leaves of Sapium insigne (ROYLE) BENTH. ex HOOK. fil. It was shown, that this compound inhibited the following processes: differentiation of 3T3-L1 preadipocytes and triglyceride accumulation in mature adipocytes, and nitric oxide production in RAW 264.7 cells.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
PubMed
SUBSTANCE RECORD
