integracin C
A benzoate ester obtained by the formal condensation of the hydroxy group of 5-(8-hydroxyundecyl)benzene-1,3-diol with 4,6-dihydroxy benzoic acid which is also substituted by a undec-7-en-1-yl group at position 6. It is isolated from Cytonaema sp. and has anti-HIV-1 activity.
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 | C35H52O6 |
|---|---|
| Charge | 0 |
| Average mass | 568.795 Da |
| Monoisotopic mass | 568.37639 Da |
| Source | ChEBI |
| InChIKey | LYMWNVVWPGMTHS-VOTSOKGWSA-N |
CCC/C=C/CCCCCCc1cc(O)cc(O)c1C(=O)OC(CCC)CCCCCCCc1cc(O)cc(O)c1
InChI=1S/C35H52O6/c1-3-5-6-7-8-9-10-13-16-20-28-24-31(38)26-33(39)34(28)35(40)41-32(18-4-2)21-17-14-11-12-15-19-27-22-29(36)25-30(37)23-27/h6-7,22-26,32,36-39H,3-5,8-21H2,1-2H3/b7-6+
Also called
- 11-(3,5-dihydroxyphenyl)undecan-4-yl 2,4-dihydroxy-6-[(7E)-undec-7-en-1-yl]benzoate
Cross-references
- reaxys:9106460
Activity roles
- HIV-1 integrase inhibitor
CHEBI:67268
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:66078 |
integracin C | antibioticmech:chebi-26ea415573 |
2026-08-30 |
Mechanism summary
- Mode of action
- VIRAL_INTEGRASE_INHIBITION microbial 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