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(1-R*,2-R*,3-E,11-R*,12-S*)-2,18-O-DIACETYL-16-O-(3-HYDROXY-3-METHYLGLUTARYL)-2,16,18-TRIHYDROXYDOLABELLA-3,8-(17)-DIEN-7-ONE

Compound with spectra: 1 NMR

(1-R*,2-R*,3-E,11-R*,12-S*)-2,18-O-DIACETYL-16-O-(3-HYDROXY-3-METHYLGLUTARYL)-2,16,18-TRIHYDROXYDOLABELLA-3,8-(17)-DIEN-7-ONE
SpectraBase Compound ID H8m5J3B7sn8
InChI InChI=1S/C30H44O10/c1-18-8-10-23-22(28(4,5)40-20(3)32)12-13-30(23,7)25(39-19(2)31)14-21(9-11-24(18)33)17-38-27(36)16-29(6,37)15-26(34)35/h14,22-23,25,37H,1,8-13,15-17H2,2-7H3,(H,34,35)/b21-14-/t22-,23+,25+,29?,30+/m1/s1
InChIKey FGKMIBOWYZLVPV-NXEAFCESSA-N
Mol Weight 564.7 g/mol
Molecular Formula C30H44O10
Exact Mass 564.293448 g/mol
Enantiomer InChIKey FGKMIBOWYZLVPV-GHXZYHPVSA-N

View Spectrum of (1-R*,2-R*,3-E,11-R*,12-S*)-2,18-O-DIACETYL-16-O-(3-HYDROXY-3-METHYLGLUTARYL)-2,16,18-TRIHYDROXYDOLABELLA-3,8-(17)-DIEN-7-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
(1-R*,2-R*,3-E,7-E11-R*,12-S*)-2,18-O-DIACETYL-16-O-(3-HYDROXY-3-METHYLGLUTARYL)-DOLABELLA-3,7-DIEN-2,16,18-TRIOL
(1-R*,2-R*,3-E,7-R*,8-S*,9-R*11-R*,12-S*)-16-O-(3-HYDROXY-3-METHYLGLUTARYL)-8,9-EPOXYDOLABELL-3-EN-2,7,16,18-TETROL
CHROZOPHOROSIDE-A1;(1R*,2R*,3E,7R*,11R*,12S*)-3,8(17)-DOLABELLADIENE-2,7,16,18-TETROL-7-O-BETA-D-GLUCOPYRANOSIDE
(1S,2S,4aR,6S,8aS)-1-(acetoxymethyl)-6-benzoyloxy-5,5,8a-trimethyl-decalin-2-carboxylic acid
LASIDIOL-PARA-METHOXYBENZOATE
Coladine
[1aR-[1aR*,4E,7R*(E),7aR*,8S*,10aS*,10bR*]]-1a,2,3,6,7,7a,8,10a,10b-decahydro-1a,5,8-trimethyl-9-oxooxireno[9,10]cyclodeca[1,2-b]furan-7-yl ester of 4-hydroxy-2-methyl-2-butenoic acid
JATAMANIN-B
10-DEANGELOYLPALLININ
CHROZOPHOROSIDE-B;(1R*,2R*,3E,7R*,8E,11R*,12S*)-3,8-DOLABELLADIENE-2,7,16,18-TETROL-7-O-BETA-D-GLUCOPYRANOSIDE
Title Journal or Book Year
3-hydroxy-3-methylglutaryl dolabellane diterpenes from Chrozophora obliqua Phytochemistry 1995

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