Examples of using Binding affinity in English and their translations into Croatian
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Relative binding affinity of anabolic-androgenic steroids.
Winstrol, another DHT derived drug,also has a binding affinity that is quite low.
In fact, its Relative Binding Affinity is so low that it cannot be effectively measured.
Trenbolone substances posses 5 times the androgen receptor binding affinity of testosterone.
Trenbolone has a very solid binding affinity for the androgen receptor also, even surpassing that of testosterone.
Trenbolone compounds posses 5 times the androgen receptor binding affinity of testosterone.
Trenbolone has a very solid binding affinity for the androgen receptor as well, also exceeding that of testosterone.
Trenbolone compounds posses 5 times the androgen receptor binding affinity of testosterone.
Trenbolone has a very solid binding affinity for the androgen receptor also, even going beyond that of testosterone.
Trenbolone substances posses five times the androgen receptor binding affinity of testosterone.
Trenbolone has a very solid binding affinity for the androgen receptor as well, even surpassing that of testosterone.
The hormone has also been shown to have an extremely strong binding affinity for the androgen receptor.
Trenbolone has an extremely strong binding affinity for the androgen receptor as well, even surpassing that of testosterone.
Trenbolone compounds posses five times the androgen receptor binding affinity of testosterone.
Trenbolone has an incredibly solid binding affinity for the androgen receptor also, even exceeding that of testosterone.
Lurasidone also exhibits partial agonism at the 5HT-1A receptor with a binding affinity of 6.38 nM.
Trenbolone has an incredibly strong binding affinity for the androgen receptor also, even going beyond that of testosterone.
It also blocks α2c-adrenergic receptors andα2a-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, also exceeding that of testosterone.
Ioflupane also binds to the serotonin transporter on 5-HT neurons butwith lower(approximately 10-fold) binding affinity.
Winstrol is a heterocyclic steroid with strong binding affinity for the androgen receptors.
The binding affinity(Ki) of eluxadoline for human κOR has not been determined; however, the Ki for guinea pig cerebellum κOR is 55 nM.
In in vitro studies, regadenoson has been shown to have little binding affinity for the A2B and A3 adenosine receptors.
Trenbolone has an exceptionally solid binding affinity for the androgen receptor too, also surpassing that of testosterone.
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.
Trenbolone has an incredibly solid binding affinity for the androgen receptor as well, 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 strong binding affinity for the androgen receptor also, also going beyond that of testosterone.
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.
Trenbolone has an extremely solid binding affinity for the androgen receptor as well, also going beyond that of testosterone.