[(3R/S)-3-CHLOROMETHYL-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-ALPHA-D-MANNOPYRANOSIDE
Compound with spectra: 1 NMR
![[(3R/S)-3-CHLOROMETHYL-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-ALPHA-D-MANNOPYRANOSIDE](/api/compound/DPHSIIE8wI0.png?ph=true&h=300&w=458 "[(3R/S)-3-CHLOROMETHYL-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOL-6-YL]-ALPHA-D-MANNOPYRANOSIDE")
| SpectraBase Compound ID | DPHSIIE8wI0 |
|---|---|
| InChI | InChI=1S/2C27H31ClN2O10/c2*1-36-18-7-12-6-16(29-20(12)25(38-3)24(18)37-2)26(35)30-10-13(9-28)15-5-4-14(8-17(15)30)39-27-23(34)22(33)21(32)19(11-31)40-27/h2*4-8,13,19,21-23,27,29,31-34H,9-11H2,1-3H3/t13-,19+,21+,22-,23-,27-;13-,19-,21-,22+,23+,27+/m01/s1 |
| InChIKey | KMUVYCFNQOOHKA-VBFCXEQZSA-N |
| Mol Weight | 1158.0 g/mol |
| Molecular Formula | C54H62Cl2N4O20 |
| Exact Mass | 1156.333446 g/mol |
| Enantiomer InChIKey | KMUVYCFNQOOHKA-MJAPXCHBSA-N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
(3R/S)-6-BENZYLOXY-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOLE
1H-Indole-3-methanol, 6-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2,3-dihydro-1-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-, .alpha.-methanesulfonate, (.+-.)-
(3R/S)-3-(TERT.-BUTYL-DIPHENYL-SILYL)-OXYMETHYL-6-HYDROXY-1-(5',6',7'-TRIMETHOXY-INDOL-2'-YL-CARBONYL)-2,3-DIHYDRO-1H-INDOLE
5H-Cycloprop[c]indol-5-one, 1,1a,2,3-tetrahydro-3-[(5,6,7-trimethoxy-1H-indol-2-yl)carbonyl]-, (.+-.)-
6-(Benzo[d][1,3]dioxol-5-yl)-3-formyl-2-hydroxy-2-methyl-5-nitro-4-phenylcyclohexanecarboxylic acid methyl ester
[5,5':7',7''-ter-1H-indole]-4,4',4''-triol, triacetate (ester)
3-Formyl-4-furyl-2-hydroxy-2-methyl-5-nitro-6-phenylcyclohexanecarboxylic acid methyl ester
#1;CALYSOLIN-XIV;11S-JALAPINOLIC-ACID-11-O-BETA-D-GLUCOPYRANOSYL-(1->3)-O-(2-O-2S,3S-NILOYL-4-O-TIGLOYL)-ALPHA-L-RHAMNOPYRANOSYL-(1->2)-[O-BETA-D-GLUCOPYRANOSY
| 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 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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