METHYL-6-DEOXY-6-[3-(5-TRIFLUOROMETHYL-2(1H)-PYRIDONE-1-YL-METHYLENE)-ANILINO]-ALPHA-D-MANNOPYRANOSIDE
Compound with spectra: 1 NMR
![METHYL-6-DEOXY-6-[3-(5-TRIFLUOROMETHYL-2(1H)-PYRIDONE-1-YL-METHYLENE)-ANILINO]-ALPHA-D-MANNOPYRANOSIDE](/api/compound/C0e5zLVN2dm.png?ph=true&h=300&w=458 "METHYL-6-DEOXY-6-[3-(5-TRIFLUOROMETHYL-2(1H)-PYRIDONE-1-YL-METHYLENE)-ANILINO]-ALPHA-D-MANNOPYRANOSIDE")
| SpectraBase Compound ID | C0e5zLVN2dm |
|---|---|
| InChI | InChI=1S/2C20H23F3N2O6/c2*1-30-19-18(29)17(28)16(27)14(31-19)8-24-13-4-2-3-11(7-13)9-25-10-12(20(21,22)23)5-6-15(25)26/h2*2-7,10,14,16-19,24,27-29H,8-9H2,1H3/t2*14-,16-,17+,18+,19+/m11/s1 |
| InChIKey | KEYMAWQOXVTAQI-QFXCHQRASA-N |
| Mol Weight | 888.81 g/mol |
| Molecular Formula | C40H46F6N4O12 |
| Exact Mass | 888.301642 g/mol |
| Enantiomer InChIKey | KEYMAWQOXVTAQI-YPDHMKHISA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
ZPMWLTJOESPRMR-GZHZPSPZSA-N
METHYL-6-(4-ACETOXYMETHYL-3-NITROBENZOYLAMINO)-6-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
#24;METHYL-6-DEOXY-6-[N'-[6-DEOXY-6-[N'-(6-AMINO-6-DEOXY-BETA-D-GLUCOPYRANOSYL)-THIOUREIDO]-6-DEOXY-BETA-D-GLUCOPYRANOSYL]-THIOUREIDO]-ALPHA-D-GLUCOPYRA
N-(METHYL-6-DEOXY-ALPHA-D-GLUCOPYRANOSID-6-YL)-N-(ETHYL-4-DEOXY-ALPHA-D-MANNOPYRANOSID-4-YL)-AMINE
N-(METHYL-6-DEOXY-ALPHA-D-MANNOPYRANOSID-6-YL)-N-(ETHYL-4-DEOXY-ALPHA-D-MANNOPYRANOSID-4-YL)-AMINE
PER-6-[(2-METHOXYETHYL)-AMINO]-6-DEOXY-BETA-CYClODEXTRIN
PER-6-[(2-HYDROXYETHYL)-AMINO]-6-DEOXY-GAMMA-CYClODEXTRIN
PER-6-[(2-HYDROXYETHYL)-AMINO]-6-DEOXY-ALPHA-CYClODEXTRIN
6-[(S)-2,3-DICAPROYL-PROPYLAMIDO-SUCCINYLAMIDO]-6-DEOXY-1,2,3,4-TETRA-O-METHYL-ALPHA-D-GLUCOPYRANOSIDE
| Title | Journal or Book | Year |
|---|---|---|
| Design, Synthesis and Antifibrotic Activities of Carbohydrate- Modified 1-(Substituted aryl)-5-trifluoromethyl-2(1H) Pyridones | Molecules | 2012 |