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#16B;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPY

Compound with spectra: 2 NMR

#16B;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPY
SpectraBase Compound ID 7kdoh1ZmZgO
InChI InChI=1S/C51H58N2O15Si/c1-29(54)62-28-42-45(64-30(2)55)47(65-31(3)56)48(66-32(4)57)50(68-42)67-35-21-22-38-34(27-63-69(51(5,6)7,36-17-13-11-14-18-36)37-19-15-12-16-20-37)26-53(40(38)25-35)49(58)39-23-33-24-41(59-8)44(60-9)46(61-10)43(33)52-39/h11-25,34,42,45,47-48,50,52H,26-28H2,1-10H3/t34?,42-,45-,47+,48-,50-/m1/s1
InChIKey IYYVYFRWWZCIEX-POTCVNKKSA-N
Mol Weight 967.1 g/mol
Molecular Formula C51H58N2O15Si
Exact Mass 966.360646 g/mol
Enantiomer InChIKey IYYVYFRWWZCIEX-LAZOCIIBSA-N

View Spectrum of #16B;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPY

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of #16B;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPY

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • #16A;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTO
#16A;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTO
#16C;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOP
Title Journal or Book Year
A strategy for tumor-selective chemotherapy by enzymatic liberation of seco-duocarmycin SA-derivatives from nontoxic prodrugs Bioorganic & Medicinal Chemistry 2001
#16A;[(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5,6,7-TRIMETHOXY-INDOL-2-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-2,3,4,6-TETRA-O-ACETYL-BETA-D-GALACTO
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