An abietane diterpenoid found in the medicinal plant Isodon rubescens that is 7α,8β-dihydroxyabiet-13-ene in which the 20-methyl group has undergone formal oxidation to the corresponding carboxy group and condensed with the 8-hydroxy group to give the corresponding γ-lactone. It has shown inhibitory activity against biofilm formation of the dental bacterium Streptococcus mutans.
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:35681CHEBI:36762CHEBI:37581CHEBI:52557CHEBI:78840| Molecular formula | C20H30O3 |
|---|---|
| Charge | 0 |
| Average mass | 318.457 Da |
| Monoisotopic mass | 318.21949 Da |
| Source | ChEBI |
| InChIKey | XAPXKNWMZURWMY-VQEGESQYSA-N |
[H][C@]12CCC(C(C)C)=C[C@@]13OC(=O)[C@@]21CCCC(C)(C)[C@]1([H])C[C@H]3O
InChI=1S/C20H30O3/c1-12(2)13-6-7-14-19-9-5-8-18(3,4)15(19)10-16(21)20(14,11-13)23-17(19)22/h11-12,14-16,21H,5-10H2,1-4H3/t14-,15+,16-,19+,20-/m1/s1
CHEBI:33282| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:138243 |
rubesanolide D | antibioticmech:chebi-486652d228 |
2026-08-30 |
Seeded from data/raw/ inventories (CHEBI)
Re-seeded from updated data/raw/ inventories
Re-seeded from updated data/raw/ inventories