(2-S)-7,8-DIHYDRO-5-HYDROXY-2-METHYL-2-(4''-METHYL-3''-PENTENYL)-8-PHENYL-2-H,6-H-BENZO-[1.2-B:5.4-B']-DIPYRAN-6-ONE
Compound with spectra: 1 NMR
![(2-S)-7,8-DIHYDRO-5-HYDROXY-2-METHYL-2-(4''-METHYL-3''-PENTENYL)-8-PHENYL-2-H,6-H-BENZO-[1.2-B:5.4-B']-DIPYRAN-6-ONE](/api/compound/IvPSyfEtqlx.png?ph=true&h=300&w=458 "(2-S)-7,8-DIHYDRO-5-HYDROXY-2-METHYL-2-(4''-METHYL-3''-PENTENYL)-8-PHENYL-2-H,6-H-BENZO-[1.2-B:5.4-B']-DIPYRAN-6-ONE")
| SpectraBase Compound ID | IvPSyfEtqlx |
|---|---|
| InChI | InChI=1S/C25H26O4/c1-16(2)8-7-12-25(3)13-11-18-21(29-25)15-22-23(24(18)27)19(26)14-20(28-22)17-9-5-4-6-10-17/h4-6,8-11,13,15,20,27H,7,12,14H2,1-3H3/t20-,25?/m0/s1 |
| InChIKey | VZUIBLOZHYYUON-JINQPTGOSA-N |
| Mol Weight | 390.48 g/mol |
| Molecular Formula | C25H26O4 |
| Exact Mass | 390.183109 g/mol |
| Enantiomer InChIKey | VZUIBLOZHYYUON-VGOKPJQXSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
VILLOSIN-A;(2S)-5,2',6'-TRIHYDROXY-2'',2''-DIMETHYLPYRANO-[5'',6'':6,7]-FLAVANONE
Obovatin methyl ether
(8S)-5-hydroxy-8-(3-hydroxy-4-methoxyphenyl)-2-(4-hydroxy-4-methylpentyl)-2-methyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-6-one
Paratocarpin J
(8S)-5-hydroxy-8-(4-hydroxy-3,5-dimethoxyphenyl)-2-(4-hydroxy-4-methylpentyl)-2-methyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-6-one
(-)-(2S)-5,3'-DIHYDROXY-4'-METHOXY-6'',6''-DIMETHYLCHROMENO-(7,8,2'',3'')-FLAVANONE
(E)-1-[7-methoxy-2-methyl-2-(4-methylpent-3-enyl)-5-trimethylsilyloxy-chromen-6-yl]-3-(4-trimethylsilyloxyphenyl)prop-2-en-1-one
LINDERATONE;EPIMER-1
5,4'-DIHYDROXY-4'',4''-DIMETHYL-5''-METHYL-5''-H-DIHYDROFURANO-[2'',3'':6,7]-FLAVANONE
(2S)-5,6,7-TRIHYDROXYFLAVANONE 7-O-beta-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Bioactive Secondary Metabolites from Boesenbergia pandurata of Myanmar and Their Preferential Cytotoxicity against Human Pancreatic Cancer PANC-1 Cell Line in Nutrient-Deprived Medium | Journal of Natural Products | 2007 |