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(+)-(7-R,7'-R,7''-R,7'''-S,8-S,8'-S,8''-S,8'''-S)-4'',4'''-DIHYDROXY-3,3',3'',3''',5,5'-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8'':4',8'''-

Compound with spectra: 1 NMR

(+)-(7-R,7'-R,7''-R,7'''-S,8-S,8'-S,8''-S,8'''-S)-4'',4'''-DIHYDROXY-3,3',3'',3''',5,5'-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8'':4',8'''-
SpectraBase Compound ID 4xu22BjCgVz
InChI InChI=1S/C42H50O16/c1-49-29-11-21(7-9-27(29)45)37(47)35(17-43)57-41-31(51-3)13-23(14-32(41)52-4)39-25-19-56-40(26(25)20-55-39)24-15-33(53-5)42(34(16-24)54-6)58-36(18-44)38(48)22-8-10-28(46)30(12-22)50-2/h7-16,25-26,35-40,43-48H,17-20H2,1-6H3/t25-,26-,35+,36+,37-,38-,39+,40+/m1/s1
InChIKey LSWNERGQFCAXLI-RBGMVGGZSA-N
Mol Weight 810.8 g/mol
Molecular Formula C42H50O16
Exact Mass 810.309886 g/mol
Enantiomer InChIKey LSWNERGQFCAXLI-YPPJHGTCSA-N

View Spectrum of (+)-(7-R,7'-R,7''-R,7'''-S,8-S,8'-S,8''-S,8'''-S)-4'',4'''-DIHYDROXY-3,3',3'',3''',5,5'-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8'':4',8'''-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
(+)-(7-R,7'-R,7''-R,7'''-R,8-S,8'-S,8''-S,8'''-S)-4'',4'''-DIHYDROXY-3,3',3'',3''',5,5'-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8'':4',8'''-
HEDYOTISOL-A
HEDYOTISOL_A
(-)-(7-R,7'-R,7''-S,8-S,8'-S,8''-S)-4',4''-DIHYDROXY-3,3',3'',5,5',5''-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8''-OXY-8,8'-SESQUINEOLIGNAN-7'',9''-DIOL
(-)-(7-R,7'-R,7''-R,8-S,8'-S,8''-S)-4',4''-DIHYDROXY-3,3',3'',5,5',5''-HEXAMETHOXY-7,9':7',9-DIEPOXY-4,8''-OXY-8,8'-SESQUINEOLIGNAN-7'',9''-DIOL
5-METHOXYSESAMIN
(+)-5'-DEMETHOXYEPIEXCELSIN
(7-S*,8-R*,7'-S*,8'-R*)-4,4'-DIMETHOXYHUAZHONGILEXIN_9-O-BETA-L-XYLOPYRANOSIDE
(7,8-trans, 8,8'-trans, 7',8'-cis)-7-(5"'-Methoxy-3''',4'''-methylenedioxyphenyl)-7'-(4"hydroxy-3",5"-dimethoxyphenyl)-8-(acetoxymethyl)-8'-(hydroxymethyl)-tetrahydroifuran
7,8-TRANS-8,8'-TRANS-7',8'-CIS-7-(5-METHOXY-3,4-METHYLENEDIOXYPHENYL)-7'-(4-HYDROXY-3,5-DIMETHOXYPHENYL)-8-ACETOXYMETHYLTETRAHYDROFURAN
Title Journal or Book Year
Lignans and Neolignans from Sinocalamus affinis and Their Absolute Configurations Journal of Natural Products 2011
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