(5R)-5-hydroxy-7-(4''-hydroxy-3''-methoxyphenyl)-1-phenyl-3-heptanone
A β-hydroxy ketone that is (5R)-5-hydroxyheptan-3-one substituted by a phenyl group at position 1 and a 4-hydroxy-3-methoxyphenyl moiety at position 7. Isolated from Alpinia officinarum, it exhibits antiviral activity against influenza 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 | C20H24O4 |
|---|---|
| Charge | 0 |
| Average mass | 328.408 Da |
| Monoisotopic mass | 328.16746 Da |
| Source | ChEBI |
| InChIKey | JHJPDDBIHSFERA-GOSISDBHSA-N |
COc1cc(CC[C@@H](O)CC(=O)CCc2ccccc2)ccc1O
InChI=1S/C20H24O4/c1-24-20-13-16(9-12-19(20)23)8-11-18(22)14-17(21)10-7-15-5-3-2-4-6-15/h2-6,9,12-13,18,22-23H,7-8,10-11,14H2,1H3/t18-/m1/s1
Also called
- (5R)-5-hydroxy-7-(4-hydroxy-3-methoxyphenyl)-1-phenylheptan-3-one
Cross-references
- cas:68622-73-1
- reaxys:5761856
Activity roles
- EC 3.2.1.18 (exo-α-sialidase) inhibitor
CHEBI:52425
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:66027 |
(5R)-5-hydroxy-7-(4''-hydroxy-3''-methoxyphenyl)-1-phenyl-3-heptanone | antibioticmech:chebi-d457318742 |
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)
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
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RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories