FR191512
A polyphenol which is the benzoate ester obtained by formal condensation of the hydroxy ester derivative produced by the successive intermolecular condensation of 3 molecules of 2,4-dihydroxy-6-(2-hydroxypropyl)benzoic acid with the carboxy OH of o-orsellinic acid. It is isolated from the Fungus strain no.17415 and exhibits activity against the infectivity of 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 | C38H38O16 |
|---|---|
| Charge | 0 |
| Average mass | 750.706 Da |
| Monoisotopic mass | 750.21599 Da |
| Source | ChEBI |
| InChIKey | HCXQIVLHUHTXGC-UHFFFAOYSA-N |
Cc1cc(O)cc(O)c1C(=O)OC(C)Cc1cc(O)cc(O)c1C(=O)OC(C)Cc1cc(O)cc(O)c1C(=O)OC(C)Cc1cc(O)cc(O)c1C(=O)O
InChI=1S/C38H38O16/c1-16-5-23(39)12-27(43)31(16)36(49)52-18(3)7-21-10-25(41)14-29(45)33(21)38(51)54-19(4)8-22-11-26(42)15-30(46)34(22)37(50)53-17(2)6-20-9-24(40)13-28(44)32(20)35(47)48/h5,9-15,17-19,39-46H,6-8H2,1-4H3,(H,47,48)
Also called
- 2-{2-[(2-{2-[(2-{2-[(2,4-dihydroxy-6-methylbenzoyl)oxy]propyl}-4,6-dihydroxybenzoyl)oxy]propyl}-4,6-dihydroxybenzoyl)oxy]propyl}-4,6-dihydroxybenzoic acid
Cross-references
- reaxys:8750768
Activity roles
- EC 3.2.1.18 (exo-α-sialidase) inhibitor
CHEBI:52425
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:65912 |
FR191512 | antibioticmech:chebi-8484ab574a |
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