An alkyl caffeate ester obtained by the formal condensation of trans-caffeic acid with nonan-2-ol. Isolated from the leaves of Piper sanguineispicum, it has been shown to exhibit antileishmanial 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.
CHEBI:65331| Molecular formula | C18H26O4 |
|---|---|
| Charge | 0 |
| Average mass | 306.402 Da |
| Monoisotopic mass | 306.18311 Da |
| Source | ChEBI |
| InChIKey | DEXGFPWDAXJBTA-WONIAPNHSA-N |
CCCCCCC[C@H](C)OC(=O)/C=C/c1ccc(O)c(O)c1
InChI=1S/C18H26O4/c1-3-4-5-6-7-8-14(2)22-18(21)12-10-15-9-11-16(19)17(20)13-15/h9-14,19-20H,3-8H2,1-2H3/b12-10+/t14-/m0/s1
CHEBI:70868| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:70484 |
(S)-1'-methyloctyl caffeate | antibioticmech:chebi-4fdb2f2426 |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories