A p-menthane monoterpenoid that is p-menth-2-ene substituted by a hydroperoxy group at position 1 and an acetyloxy group at position 8 (the 1R,4S stereoisomer). Isolated from the leaves of Laurus nobilis, it exhibits trypanocidal 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:25186CHEBI:35924CHEBI:47622| Molecular formula | C12H20O4 |
|---|---|
| Charge | 0 |
| Average mass | 228.288 Da |
| Monoisotopic mass | 228.13616 Da |
| Source | ChEBI |
| InChIKey | VIUQTXYGNHOJBD-PWSUYJOCSA-N |
CC(=O)OC(C)(C)[C@@H]1C=C[C@](C)(OO)CC1
InChI=1S/C12H20O4/c1-9(13)15-11(2,3)10-5-7-12(4,16-14)8-6-10/h5,7,10,14H,6,8H2,1-4H3/t10-,12+/m1/s1
CHEBI:36335| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:66035 |
(1R,4S)-1-hydroperoxy-p-menth-2-en-8-ol acetate | antibioticmech:chebi-119523e84a |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories