(-)-(3AS,6Z,11S,11AS)-3A,4,5,8,9,10,11,11A-OCTAHYDRO-11-HYDROXY-6-METHYL-3,10-BIS-(METHYLENE)-CYCLODECA-[B]-FURAN-2-(3H)-ONE
Compound with spectra: 1 NMR
![(-)-(3AS,6Z,11S,11AS)-3A,4,5,8,9,10,11,11A-OCTAHYDRO-11-HYDROXY-6-METHYL-3,10-BIS-(METHYLENE)-CYCLODECA-[B]-FURAN-2-(3H)-ONE](/api/compound/92oxg0JDSjR.png?ph=true&h=300&w=458 "(-)-(3AS,6Z,11S,11AS)-3A,4,5,8,9,10,11,11A-OCTAHYDRO-11-HYDROXY-6-METHYL-3,10-BIS-(METHYLENE)-CYCLODECA-[B]-FURAN-2-(3H)-ONE")
| SpectraBase Compound ID | 92oxg0JDSjR |
|---|---|
| InChI | InChI=1S/C15H20O3/c1-9-5-4-6-10(2)13(16)14-12(8-7-9)11(3)15(17)18-14/h5,12-14,16H,2-4,6-8H2,1H3/b9-5-/t12-,13-,14+/m1/s1 |
| InChIKey | MDKQKZYVYAZGOH-KRDHWONMSA-N |
| Mol Weight | 248.32 g/mol |
| Molecular Formula | C15H20O3 |
| Exact Mass | 248.141245 g/mol |
| Enantiomer InChIKey | MDKQKZYVYAZGOH-HOVXAYOCSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(-)-(3AS,6Z,9Z,11S,11AS)-3A,4,5,8,11,11A-HEXAHYDRO-11-HYDROXY-5,10-DIMETHYL-3-METHYLENECYCLODECA-[B]-FURAN-2-(3H)-ONE
Oxireno[9,10]cyclotetradeca[1,2-b]furan-9(1aH)-one, 2,3,6,7,7a,8,10a,13,14,14a-decahydro-1a,5,12-trimethyl-8-methylene-, [1aS-(1aR*,4E,7aR*,10aR*,11E,14aR*)]-
3(R)-Hydroxy-cembra-4,7,11,15(17)-tetraen-16,14-olide
(-)-14-DEOXYCRASSIN
LOBOCRASSIN-B
1,2-Dihydroxygermacra-4,10(14),11-trien-6,7H,12,6-olide
LUCENTOLIDE
Ridentin
(1R*,7S*,14S*,3E,11E)-18-ACETOXY-7-HYDROPEROXYCEMBRA-3,8(19),11,15(17)-TETRAEN-16,14-OLIDE
acetic acid [(1R,4E,6S,8E,10S,12E,14S)-10-hydroxy-16-keto-4,8,12-trimethyl-17-methylene-15-oxabicyclo[12.3.0]heptadeca-4,8,12-trien-6-yl] ester
| Title | Journal or Book | Year |
|---|---|---|
| Parthenolide and its photochemically synthesized 1(10) Z isomer: chemical reactivity and structure–activity relationship studies in human leucocyte chemotaxis | Bioorganic & Medicinal Chemistry | 2003 |