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#B1;2-AMINO-4-[1-(CARBOXYMETHYL-CARBAMOYL)-2-[5-(2-CHLOROBENZYL)-1-OXO-1,2,4,5,6,7-HEXAHYDRO-1-LAMBDA*4*-THIENO-[3,2-C]-PYRIDIN-7A-YL-SULFANYL]-ETHYLCARBAMOYL-

Compound with spectra: 1 NMR

#B1;2-AMINO-4-[1-(CARBOXYMETHYL-CARBAMOYL)-2-[5-(2-CHLOROBENZYL)-1-OXO-1,2,4,5,6,7-HEXAHYDRO-1-LAMBDA*4*-THIENO-[3,2-C]-PYRIDIN-7A-YL-SULFANYL]-ETHYLCARBAMOYL-
SpectraBase Compound ID 1iCNVEInuQQ
InChI InChI=1S/C24H31ClN4O7S2/c25-17-4-2-1-3-15(17)12-29-9-8-24(16(13-29)7-10-38(24)36)37-14-19(22(33)27-11-21(31)32)28-20(30)6-5-18(26)23(34)35/h1-4,7,18-19H,5-6,8-14,26H2,(H,27,33)(H,28,30)(H,31,32)(H,34,35)/t18-,19-,24?,38?/m0/s1
InChIKey FHFPPBFFNMCOPR-IGLWLYGPSA-N
Mol Weight 587.11 g/mol
Molecular Formula C24H31ClN4O7S2
Exact Mass 586.132269 g/mol
Enantiomer InChIKey FHFPPBFFNMCOPR-QOGSKAOUSA-N

View Spectrum of #B1;2-AMINO-4-[1-(CARBOXYMETHYL-CARBAMOYL)-2-[5-(2-CHLOROBENZYL)-1-OXO-1,2,4,5,6,7-HEXAHYDRO-1-LAMBDA*4*-THIENO-[3,2-C]-PYRIDIN-7A-YL-SULFANYL]-ETHYLCARBAMOYL-

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
(2S*,5S*)-Methyl 5-(2-1H-indol-3-ylacetylamino)-1-(4-methoxybenzyl)-5-methyl-6-oxo-2-piperidinecarboxylate
(5Z)-3-(4-chlorobenzyl)-5-({1-[2-(4-morpholinyl)-2-oxoethyl]-1H-indol-3-yl}methylene)-2,4-imidazolidinedione
1H-isoindol-1-one, 2-[(2-chlorophenyl)methyl]-3-[(2,4-difluorophenyl)amino]-2,3-dihydro-
2-[3-(2-chlorobenzyl)-5-oxo-1-phenyl-2-thioxo-4-imidazolidinyl]-N-(2,4-dimethylphenyl)acetamide
ISOPROPYL-2-DIMETHOXYMETHYL-3-METHOXYCARBONYL-6-METHYL-4-(4-NITROPHENYL)-1,4-DIHYDROPYRIDINE-5-CARBOXYLATE
2-(2-chlorophenyl)-3-(cycloheptylideneamino)-2,3-dihydro-4(1H)-quinazolinone
SFBCDKRYDKUEDJ-LJWNLINESA-N
2-bromo-N-[(Z)-1-[(6-oxo-7,11-diazatricyclo[7.3.1.0~2,7~]trideca-2,4-dien-11-yl)carbonyl]-2-(2-thienyl)ethenyl]benzamide
HELIOFERINE-B
2-{[4-methyl-5-(2-phenyl-4-quinolinyl)-4H-1,2,4-triazol-3-yl]sulfanyl}acetamide
Title Journal or Book Year
Metabolism of Ticlopidine in Rats: Identification of the Main Biliary Metabolite as a Glutathione Conjugate of Ticlopidine S-Oxide Drug Metabolism and Disposition 2009
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