<p>Direct comparison of the C1 inhibitor potentiation by test compounds with differing glycan structure.</p
SIGLEAvailable from British Library Document Supply Centre-DSC:D199916 / BLDSC - British Library Doc...
<p>Single-point inhibition data for rhodesain (Y-axis, % inhibition at 0.1 µM test compound) as comp...
<p>Comparison of biochemical parameters according to components of Med-DQI in healthy control group....
<p>The C1s activity was measured in the presence of C1-INH and test compounds (final concentration: ...
<p>The C1s activity was measured in the presence of C1-INH and test compound by a chromogenic substr...
<p>The C1s activity was measured in the absence and presence of C1-INH and test compounds (final con...
Title Potentiation of C1 inhibitor by glycosaminoglycans: dextran sulfate species are effective inhi...
<p>The examined test compounds for TS inhibition, their reference numbers, structures, and manufactu...
<div><p>The serpin C1 inhibitor (C1-INH) is the only regulator of classical complement activation as...
<p>Specificity of various purine inhibitors for different glycosylase-substrate combinations as dete...
In cell culture systems with aqueous buffers, concentration-re-sponse curves to lipophilic inhibitor...
<p>Inhibition of tested proteases by compounds Camostat, “Novartis166” and “Novartis848”.</p
<p>Each row represents the comparison of the 2D chemical structure between a molecule predicted as a...
<p>Compounds tested for their ability to overcome the anti-myogenic effect of TGF-β1 in C2C12 cells....
<p>Chemical structures of cyclic polyarginine peptides tested as furin inhibitors.</p
SIGLEAvailable from British Library Document Supply Centre-DSC:D199916 / BLDSC - British Library Doc...
<p>Single-point inhibition data for rhodesain (Y-axis, % inhibition at 0.1 µM test compound) as comp...
<p>Comparison of biochemical parameters according to components of Med-DQI in healthy control group....
<p>The C1s activity was measured in the presence of C1-INH and test compounds (final concentration: ...
<p>The C1s activity was measured in the presence of C1-INH and test compound by a chromogenic substr...
<p>The C1s activity was measured in the absence and presence of C1-INH and test compounds (final con...
Title Potentiation of C1 inhibitor by glycosaminoglycans: dextran sulfate species are effective inhi...
<p>The examined test compounds for TS inhibition, their reference numbers, structures, and manufactu...
<div><p>The serpin C1 inhibitor (C1-INH) is the only regulator of classical complement activation as...
<p>Specificity of various purine inhibitors for different glycosylase-substrate combinations as dete...
In cell culture systems with aqueous buffers, concentration-re-sponse curves to lipophilic inhibitor...
<p>Inhibition of tested proteases by compounds Camostat, “Novartis166” and “Novartis848”.</p
<p>Each row represents the comparison of the 2D chemical structure between a molecule predicted as a...
<p>Compounds tested for their ability to overcome the anti-myogenic effect of TGF-β1 in C2C12 cells....
<p>Chemical structures of cyclic polyarginine peptides tested as furin inhibitors.</p
SIGLEAvailable from British Library Document Supply Centre-DSC:D199916 / BLDSC - British Library Doc...
<p>Single-point inhibition data for rhodesain (Y-axis, % inhibition at 0.1 µM test compound) as comp...
<p>Comparison of biochemical parameters according to components of Med-DQI in healthy control group....
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