ganoderone C
A tetracyclic triterpenoid that is 5α-lanosta-8-ene with an epoxy group across positions 24 and 25, a hydroxy group at position 26 and oxo groups at positions 3 and 7. Isolated from the fruiting bodies of Ganoderma pfeifferi, it exhibits antiviral activity against influenza A 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.
Classification
Chemical structure
| Molecular formula | C30H46O4 |
|---|---|
| Charge | 0 |
| Average mass | 470.694 Da |
| Monoisotopic mass | 470.33961 Da |
| Source | ChEBI |
| InChIKey | DHGMYNLRIYMOGS-ZWETUDJHSA-N |
[H][C@@]12CC(=O)C3=C(CC[C@@]4(C)[C@@]3(C)CC[C@]4([H])[C@H](C)CCC3OC3(C)CO)[C@@]1(C)CCC(=O)C2(C)C
InChI=1S/C30H46O4/c1-18(8-9-24-30(7,17-31)34-24)19-10-15-29(6)25-20(11-14-28(19,29)5)27(4)13-12-23(33)26(2,3)22(27)16-21(25)32/h18-19,22,24,31H,8-17H2,1-7H3/t18-,19-,22+,24?,27-,28-,29+,30?/m1/s1
Also called
- 26-hydroxy-24,25-epoxylanost-8-ene-3,7-dione
- 5α-lanosta-8-ene-24,25-epoxy-26-hydroxy-3,7-dione
Cross-references
- reaxys:15775258
Activity roles
- EC 3.2.1.18 (exo-α-sialidase) inhibitor
CHEBI:52425
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65946 |
ganoderone C | antibioticmech:chebi-b25f44087e |
2026-08-30 |
Mechanism summary
- Mode of action
- VIRAL_RELEASE_INHIBITION host shared target
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories