COCONUT Compound

methyl 2-[(1~{S},2~{R},4~{S},7~{S},8~{S},11~{R},12~{R},13~{S},16~{S},18~{R})-7-(3-furyl)-18-hydroxy-1,8,12,15,15-pentamethyl-5,17-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate

CNP0132985.2 · C27H34O9 · View on COCONUT ↗

Identifiers

Namemethyl 2-[(1~{S},2~{R},4~{S},7~{S},8~{S},11~{R},12~{R},13~{S},16~{S},18~{R})-7-(3-furyl)-18-hydroxy-1,8,12,15,15-pentamethyl-5,17-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate
IUPAC Namemethyl 2-[(1~{S},2~{R},4~{S},7~{S},8~{S},11~{R},12~{R},13~{S},16~{S},18~{R})-7-(3-furyl)-18-hydroxy-1,8,12,15,15-pentamethyl-5,17-dioxo-3,6,14-trioxapentacyclo[9.7.0.0^{2,4}.0^{2,8}.0^{12,16}]octadecan-13-yl]acetate
COCONUT IDCNP0132985.2
InChIKeyQZEZEIDFGQZYKE-SYIIKYOPSA-N
InChIInChI=1S/C27H34O9/c1-23(2)18-17(29)19(30)26(5)14(25(18,4)15(35-23)11-16(28)32-6)7-9-24(3)20(13-8-10-33-12-13)34-22(31)21-27(24,26)36-21/h8,10,12,14-15,18-21,30H,7,9,11H2,1-6H3/t14-,15+,18-,19+,20+,21-,24+,25+,26+,27-/m1/s1
SMILESCOC(=O)C[C@@H]1OC(C)(C)[C@H]2C(=O)[C@H](O)[C@]3(C)[C@H](CC[C@@]4(C)[C@H](C5=COC=C5)OC(=O)[C@H]5O[C@@]534)[C@@]12C

Properties

Molecular FormulaC27H34O9
Molecular Weight502.56
Exact Mass502.22028
Log P (ALogP)2.74
TPSA124.80
H-Bond Donors / Acceptors1 / 9
Rotatable Bonds3
Lipinski's Rule of 5 Violations1
QED Drug-likeness0.49
NP-likeness3.02

Classification

NP PathwayTerpenoids
NP SuperclassTriterpenoids
NP ClassLimonoids
Chemical SuperclassLipids and lipid-like molecules
Chemical ClassSteroids and steroid derivatives
Chemical SubclassSteroid lactones

Reported in GR-MAPs Plants

Salvia officinalis as “Salvia officinalis” in COCONUT

Data from COCONUT (COlleCtion of Open Natural prodUcTs), released under CC0. Chandrasekhar V. et al. COCONUT 2.0: a comprehensive overhaul and curation of the collection of open natural products database. Nucleic Acids Research (2024), doi:10.1093/nar/gkae1063. COCONUT release 2026-10.