A tetracyclic triterpenoid that is 5α-lanosta-8,24-diene substituted by a hydroxy group at position 26 and oxo groups at positions 3 and 7. Isolated from the fruiting bodies of Ganoderma pfeifferi, it exhibits against herpes simplex virus.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
CHEBI:15734CHEBI:26893CHEBI:46640| Molecular formula | C30H46O3 |
|---|---|
| Charge | 0 |
| Average mass | 454.695 Da |
| Monoisotopic mass | 454.3447 Da |
| Source | ChEBI |
| InChIKey | SDAWCNCFVWQZDP-GOUGDUPLSA-N |
[H][C@@]12CC(=O)C3=C(CC[C@@]4(C)[C@@]3(C)CC[C@]4([H])[C@H](C)CC/C=C(\C)CO)[C@@]1(C)CCC(=O)C2(C)C
InChI=1S/C30H46O3/c1-19(18-31)9-8-10-20(2)21-11-16-30(7)26-22(12-15-29(21,30)6)28(5)14-13-25(33)27(3,4)24(28)17-23(26)32/h9,20-21,24,31H,8,10-18H2,1-7H3/b19-9+/t20-,21-,24+,28-,29-,30+/m1/s1
CHEBI:64953| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65945 |
ganoderone A | antibioticmech:chebi-4034d7e2cd |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories