AMIKACIN
Compound with spectra: 2 NMR
| SpectraBase Compound ID | 7syEsNo9Wvm |
|---|---|
| InChI | InChI=1S/C22H43N5O13/c23-2-1-8(29)20(36)27-7-3-6(25)18(39-22-16(34)15(33)13(31)9(4-24)37-22)17(35)19(7)40-21-14(32)11(26)12(30)10(5-28)38-21/h6-19,21-22,28-35H,1-5,23-26H2,(H,27,36)/t6-,7+,8-,9+,10+,11-,12+,13+,14+,15-,16+,17-,18+,19-,21+,22+/m0/s1 |
| InChIKey | LKCWBDHBTVXHDL-RMDFUYIESA-N |
| Mol Weight | 585.6 g/mol |
| Molecular Formula | C22H43N5O13 |
| Exact Mass | 585.285736 g/mol |
| Enantiomer InChIKey | LKCWBDHBTVXHDL-DNKKMLDDSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | D2O;PH=2 |
(S)-2'''-DEOXY-2'''-FLUORO-AMIKACIN;1-N-[(S)-4-AMINO-2-FLUORO-BUTYRYL]-KANAXYCIN-A
3'-DEOXY-AMIKACIN
2',3'-DIDEOXY-AMIKACIN
6''-CHLORO-3',6''-DIDEOXY-AMIKACIN
6''-CHLORO-2',3',6''-TRIDEOXY-AMIKACIN
1-N-[(S)-4-AMINO-2-FLUOROBUTYRYL]-DIBEKACIN
4'-DEOXYBUTIROSIN-A
5''-DEOXY-4',5''-DIDEOXYBUTIROSIN-A
#18;3-AMINOPROPYL_BETA-D-GALACTOPYRANOSYL-(1-3)-2-ACETAMIDO-2-DEOXY-BETA-D-GALACTOPYRANOSYL-(1-3)-ALPHA-D-GALACTOPYRANOSYL-(1-4)-BETA-D-GALACTOPYRANOSYL-(1-4)-
| Title | Journal or Book | Year |
|---|---|---|
| The Novel Enzymatic 3"-N-Acetylation of Arbekacin by an Aminoglycoside 3-N-Acetyltransferase of Streptomyces Origin and the Resulting Activity. | The Journal of Antibiotics | 1998 |
| Synthesis and biological activity of 1-N-(4-(substituted)amidino and guanidino-2-hydroxybutyryl)kanamycins A and B. | The Journal of Antibiotics | 1991 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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KnowItAll IR, Raman, and UV-Vis Spectral Libraries
Author: Wiley
The KnowItAll IR, Raman, and UV-Vis spectral libraries offer access to the world's largest collection of IR, Raman, and UV-Vis spectra, including the renowned Sadtler spectra. The libraries include a wide range of compounds from pure organics to industrial compounds. Learn more.