[((2'R,3'S,4'S)-3'-ACETAMIDO-4'-HYDROXY-2'-[(1''S,2''R)-1'',2'',3''-TRIHYDROXYPROPYL]-PYRROLIDIN-1'-YL)-METHYL]-PHOSPHONIC-ACID
Compound with spectra: 1 NMR
![[((2'R,3'S,4'S)-3'-ACETAMIDO-4'-HYDROXY-2'-[(1''S,2''R)-1'',2'',3''-TRIHYDROXYPROPYL]-PYRROLIDIN-1'-YL)-METHYL]-PHOSPHONIC-ACID](/api/compound/EHAhYugaLWy.png?ph=true&h=300&w=458 "[((2'R,3'S,4'S)-3'-ACETAMIDO-4'-HYDROXY-2'-[(1''S,2''R)-1'',2'',3''-TRIHYDROXYPROPYL]-PYRROLIDIN-1'-YL)-METHYL]-PHOSPHONIC-ACID")
| SpectraBase Compound ID | EHAhYugaLWy |
|---|---|
| InChI | InChI=1S/C10H21N2O8P/c1-5(14)11-8-6(15)2-12(4-21(18,19)20)9(8)10(17)7(16)3-13/h6-10,13,15-17H,2-4H2,1H3,(H,11,14)(H2,18,19,20)/t6-,7?,8+,9+,10?/m0/s1 |
| InChIKey | LVEHCZXRPYGQGU-KRVLYJGESA-N |
| Mol Weight | 328.26 g/mol |
| Molecular Formula | C10H21N2O8P |
| Exact Mass | 328.103553 g/mol |
| Enantiomer InChIKey | LVEHCZXRPYGQGU-RAWPOXPZSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O |
(4-ACETAMIDO-2,4-DIDEOXY-D-GLYCERO-BETA-D-GALACTOOCTOPYRANOSYL)-PHOSPHONIC-ACID
(4-ACETAMIDO-2,4-DIDEOXY-D-GLYCERO-ALPHA-D-GALACTOOCTOPYRANOSYL)-PHOSPHONIC-ACID
TERT.-BUTYL-5-ACETAMIDO-2,6-ANHYDRO-3,5-DIDEOXY-D-ERYTHRO-L-MANNO-NONONAT
(2R,4S,5R,6R)-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]tetrahydropyran-2-carboxylic acid tert-butyl ester
1-(2-Fluoroethyl)-1,5,6,7,8,8a-hexahydro-6,7,8-trihydroxy-3H-oxazolo[3,4-a]pyridin-3-one
(1S,6S,7R,8R,8aR)-1-(2'-Chloroethyl)-1,5,6,7,8,8a-hexahydro-6,7,8-trihydroxy-3H-oxazolo[3,4-a]pyridin-3-one
1-(2-Hydroxyethyl)-1,5,6,7,8,8a-hexahydro-6,7,8-trihydroxy-3H-oxazolo[3,4-a]pyridin-3-one
Benzyl 2,3-bis(acetylamino)-2,3-dideoxyhexopyranoside
BENZYL 2,3-DIACETAMIDO-2,3-DEOXY-ALPHA-D-GLUCOPYRANOSIDE
METHYL-N-ACETYL-ALPHA-D-NEURAMINIC-ACID
| Title | Journal or Book | Year |
|---|---|---|
| Synthesis of Pyrrolidine Analogues ofN-Acetylneuraminic Acid as Potential Sialidase Inhibitors | Helvetica Chimica Acta | 1990 |