In a study by Marsaioli et al. the tranport of the antibiotic fosfomycin was shown to be facilitated by a an active proteic transport system, rather than via passive diffusion through the phospohlipidic membranes. The did this by employing STD-NMR, which showed a prefered interaction between specific parts of the fosfomycin molecule (otherwise known as an epitope) and Human serum albumin (HSA). H Hạc H3C PO3NA2 fosfomycin The below spectra are the A off- resonance (set at 30ppm) and B the on-resonance spectrum (set at -0.5ppm). The signal at 3.2ppm is a multiplet. The signal at 2.7ppm is a doublet of doublets and signal at 1.4ppm is a poorly resolved doublet. Th 3 S.5 5.0 4.5 4.0 3.5 3.D 2.5 2.0 1.5 1.0 0.5 Ppm
In a study by Marsaioli et al. the tranport of the antibiotic fosfomycin was shown to be facilitated by a an active proteic transport system, rather than via passive diffusion through the phospohlipidic membranes. The did this by employing STD-NMR, which showed a prefered interaction between specific parts of the fosfomycin molecule (otherwise known as an epitope) and Human serum albumin (HSA). H Hạc H3C PO3NA2 fosfomycin The below spectra are the A off- resonance (set at 30ppm) and B the on-resonance spectrum (set at -0.5ppm). The signal at 3.2ppm is a multiplet. The signal at 2.7ppm is a doublet of doublets and signal at 1.4ppm is a poorly resolved doublet. Th 3 S.5 5.0 4.5 4.0 3.5 3.D 2.5 2.0 1.5 1.0 0.5 Ppm
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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3
![in a study by Marsaioli et al. the tranport of the antibiotic fosfomycin was shown to be facilitatec
by a an active proteic transport system, rather than via passive diffusion through the
phospohlipidic membranes. The did this by employing STD-NMR, which showed a prefered
interaction between specific parts of the fosfomycin molecule (otherwise known as an epitope)
and Human serum albumin (HSA).
H
H)
Hạc
H3C
fosfomycin
The below spectra are the A off- resonance (set at 30ppm) and B the on-resonance spectrum
(set at -0.5ppm). The signal at 3.2ppm is a multiplet. The signal at 2.7ppm is a doublet of
doublets and signal at 1.4ppm is a poorly resolved doublet.
Th
3
S.5
5.0
4.5
4.0
3.5
3.0
2.5
2.0
1.5
1.0
0.5
Figure 1](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F83ae3fb9-1c11-4f71-8a0d-474834ecd625%2Fa78cd3e2-d0f7-4705-9318-83057f6f21ce%2Fzyodhvm_processed.jpeg&w=3840&q=75)
Transcribed Image Text:in a study by Marsaioli et al. the tranport of the antibiotic fosfomycin was shown to be facilitatec
by a an active proteic transport system, rather than via passive diffusion through the
phospohlipidic membranes. The did this by employing STD-NMR, which showed a prefered
interaction between specific parts of the fosfomycin molecule (otherwise known as an epitope)
and Human serum albumin (HSA).
H
H)
Hạc
H3C
fosfomycin
The below spectra are the A off- resonance (set at 30ppm) and B the on-resonance spectrum
(set at -0.5ppm). The signal at 3.2ppm is a multiplet. The signal at 2.7ppm is a doublet of
doublets and signal at 1.4ppm is a poorly resolved doublet.
Th
3
S.5
5.0
4.5
4.0
3.5
3.0
2.5
2.0
1.5
1.0
0.5
Figure 1
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