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The XPS data of the O 1 s level display the chemical bonding of carboxyl acid, and the peak position of the Cd 3d level is not shifted after annealing.
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Introduction of l-arginine, a positively charged amino acid, at the X4 position of the C-terminus resulted in an increase in binding affinity (LXY30 vs LXY4).
The line at 90° simulates a straight up and down position of the C-arm.
The ratio Δ/R determines the position of the c P maximum in terms of nanoparticle concentration.
The binding energy (BE) was calibrated with the position of the C 1 s peak at 284.8 eV.
The position of the Cs MOT is overlapped with the Rb MOT as both use the same coil system.
In addition, the IR peak position of the c-BN reststrahlen band was determined for adherent coatings and after the films completely peeled off the substrate.
The three-dimensional structure of BtGH115A reveals that BtGH115A has the same domain architecture as the other structurally characterized member of this family, BoAgu115A; however the position of the C-terminal module is altered with respect to each individual enzyme.
A group of (E -and (Z)-1,2,3-triaryl-2-propE -andne derivatives possessing a methylsulfonyl COX-2 pharmacophore at the para position of the C-1 phenyl ring were synthesiZ -1,2,3-triaryl-2-propen-1-oneCOX-2 inhibitors.
A group of 4-carboxyl quinoline derivatives possessing a methylsulfonyl COX-2 pharmacophore at the para position of the C-2 phenyl ring were designed and synthesized as selective COX-2 inhibitors.
The binding energy of the adventitious carbon (C 1 s) line at 284.6 eV was used for calibration, and the positions of other peaks were corrected according to the position of the C 1 s signal.
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