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THIELAVIN-J;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-HYDROXY-3,6-DIMETHYLBENZOIC-ACID

Compound with spectra: 1 NMR

THIELAVIN-J;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-HYDROXY-3,6-DIMETHYLBENZOIC-ACID
SpectraBase Compound ID 18PU6xXj8qX
InChI InChI=1S/C29H30O10/c1-11-9-18(30)15(5)23(31)21(11)28(35)39-25-14(4)13(3)22(26(37-8)17(25)7)29(36)38-19-10-12(2)20(27(33)34)24(32)16(19)6/h9-10,30-32H,1-8H3,(H,33,34)
InChIKey RLLCMRPOSFZYJJ-UHFFFAOYSA-N
Mol Weight 538.55 g/mol
Molecular Formula C29H30O10
Exact Mass 538.183897 g/mol

View Spectrum of THIELAVIN-J;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-METHOXYBENZOYLOXY]-2-HYDROXY-3,6-DIMETHYLBENZOIC-ACID

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C5D5N
THIELAVIN-N;4-[4'-(2'',4''-DIHYDROXY-3'',6''-DIMETHYLBENZOYLOXY)-3',5',6'-TRIMETHYL-2'-HYDROXYBENZOYLOXY]-2-METHOXY-5,6-DIMETHYLBENZOIC-ACID
Benzoic acid, 3-chloro-6-methoxy-2,5-dimethyl-4-(phenylmethoxy)-, 3-methoxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
Benzoic acid, 3-chloro-2,5-dimethyl-4,6-bis(phenylmethoxy)-, 3-methoxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
Benzoic acid, 3-chloro-4-methoxy-2,5-dimethyl-6-(phenylmethoxy)-, 3-hydroxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
Benzoic acid, 3-chloro-2,5-dimethyl-4,6-bis(phenylmethoxy)-, 3-hydroxy-4-(methoxycarbonyl)-2,5,6-trimethylphenyl ester
AGONODEPSIDE-B
Methyl 4-(4'-benzyloxy-3'-chloro-6'-hydroxy-2'-methylbenzoyloxy)-2-hydroxy-5-methoxy-3,6-dimethylbenzoate
1,3-Benzenedicarboxylic acid, 2-hydroxy-4-methoxy-6-methyl-, 1-(3-carboxy-4,6-dihydroxy-2,5-dimethylphenyl) ester
Benzoic acid, 3-formyl-5-[(3-formyl-2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-2,4-di hydroxy-6-methyl-
Methyl 4-acetoxy-5-(3'-acetoxy-2',5'-dimethylphenoxy)-2-hydroxy-3,6-dimethylbenzoate
Title Journal or Book Year
Thielavins as Glucose-6-phosphatase (G6Pase) Inhibitors: Producing Strain, Fermentation, Isolation, Structural Elucidation and Biological Activities. The Journal of Antibiotics 2002
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