Examples of using Binding affinity in English and their translations into Romanian
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This is possible due to its binding affinity for SHBG.
Increased binding affinity antibodies(affinity maturation).
In in vitro studies, regadenoson has been shown to have little binding affinity for the A2B and A3 adenosine receptors.
Ioflupane also binds to the serotonin transporter on 5-HT neurons but with lower(approximately 10-fold) binding affinity.
Dianabol has a similarly low binding affinity, and also produces a very good anabolic response.
Lurasidone also exhibits partial agonism at the 5HT-1A receptor with a binding affinity of 6.38 nM.
Anavar is another anabolic steroid that has less binding affinity for the androgen receptor than other compounds like Dbol.
The binding affinity of 4-hydroxymethyl ambrisentan for the human endothelin receptor is 65-fold less than ambrisentan.
Nandrolone has a relatively long half-life in the plasma and a strong binding affinity for androgen receptors.
Trenbolone has an incredibly solid binding affinity for the androgen receptor also, also exceeding that of testosterone.
It also blocks α2c-adrenergic receptors and α2a-adrenergic receptors with a binding affinity of 10.8 and 40.7 nM respectively.
Trenbolone has an extremely strong binding affinity for the androgen receptor also, even exceeding that of testosterone.
Dialysis may not be effective in removing tolvaptan because of its high binding affinity for human plasma protein(> 98%).
Trenbolone has an incredibly solid binding affinity for the androgen receptor also, also exceeding that of testosterone.
Although progesterone is a c-19 steroid, removal of this group as in 19-norprogesterone creates a hormone with greater binding affinity for its corresponding receptor.
Trenbolone has an exceptionally solid binding affinity for the androgen receptor too, also exceeding that of testosterone.
It is a humanized monoclonal antibody fragment(Fab) that binds to dabigatran with very high affinity, approximately 300-fold more potent than the binding affinity of dabigatran for thrombin.
Trenbolone has an incredibly solid binding affinity for the androgen receptor also, even exceeding that of testosterone.
The end result of the aforementioned modifications is that IGF-1 LR3 produces the same activities at the IGF-1 receptor in the tissues of the body that IGF-1 does, butalso enjoys a significantly lower binding affinity for the IGF binding proteins that were discussed earlier.
Interferon beta-1b both decreases the binding affinity and enhances the internalisation and degradation of the interferon-gamma receptor.
The most abundant metabolites of tasimelteon have less than one- tenth of the binding affinity of the parent molecule for both the MT1 and MT2 receptors.
The binding affinity of 99mTc-depreotide to SSTR was shown in studies of pancreatic tumours in Lewis rats and in vitro in human tumour membranes.
In vitro, florbetaben(18F)shows nanomolar binding affinity to synthetic β-amyloid fibrils and to AD brain homogenate.
The binding affinity(Ki) of eluxadoline for human κOR has not been determined; however, the Ki for guinea pig cerebellum κOR is 55 nM.
Palonosetron is a 5-HT3 receptor antagonist with a strong binding affinity for this receptor and little or no affinity for other receptors.
For toremifene, which has a relatively high binding affinity for sugammadex and for which relatively high plasma concentrations might be present, some displacement of vecuronium or rocuronium from the complex with sugammadex could occur.
Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for muscarinic receptors.
Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for cholinergic muscarinic receptors.
Even though oxymetholone possesses very low binding affinity when it comes to the androgen receptor, this steroid is still a very effective option for promoting significant gains in body mass.
The information in this section is based on binding affinity between sugammadex and other medicinal products, non-clinical experiments and simulations using a model taking into account the pharmacodynamic effect of neuromuscular blocking agents and the pharmacokinetic interaction between neuromuscular blocking agents and sugammadex.