Examples of using Binding affinity in English and their translations into Portuguese
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ITC is particularly useful as it gives not only the binding affinity, but also the thermodynamics of the binding. .
Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site
In fact, its Relative Binding Affinity is so low that it cannot be effectively measured.
Trenbolone has an exceptionally solid binding affinity for the androgen receptor also,
Trenbolone has a very strong binding affinity for the androgen receptor also,
For example, it is possible to calculate digitally what changes could improve the drug candidate's binding affinity, i.e.
Abstract The prediction of the binding affinity has been a computational challenge,
The prediction of the binding affinity has been a computational challenge,
The binding affinity(Ki) of eluxadoline for human κOR has not been determined;
Lurasidone binds strongly to dopaminergic D2- and to serotonergic 5-HT2A and 5-HT7- receptors with high binding affinity of 0.994, 0.47 and 0.495 nM, respectively.
Dialysis may not be effective in removing tolvaptan because of its high binding affinity for human plasma protein> 98.
In in vitro studies, regadenoson has been shown to have little binding affinity for the A2B and A3 adenosine receptors.
CXCL8 is a member of the CXC chemokine family that shows high binding affinity to CXCR1 IL-8 receptor type 1 and CXCR2 IL-8 receptor type 2.
This protein has binding affinity for c3b and c4b factors by inhibiting the formation of c3 convertase via both the classical
One typical problem in cheminformatics is to predict the binding affinity of drug molecules to a given target.
ITC is one of the latest techniques to be used in characterizing binding affinity of ligands for proteins.
Despite very low binding affinity with the androgen receptor,
is the more active enantiomer due to its greater binding affinity to acetylcholinesterase.
RNA with specific binding affinity for a target molecule.
SARS-CoV in the S1 unit of the S protein implicates that the binding affinity of its S protein with human ACE2 might have altered.