Examples of using Binding affinity in English and their translations into Bulgarian
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Oxymetholone does not have much binding affinity for the androgen receptor.
It is this binding affinity of THC for this receptor that leads to the psychoactive effects of the THC.
The most notable characteristic of this steroid is its binding affinity to SHBG.
Ciclesonide exhibits low binding affinity to the glucocorticoid-receptor.
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.
Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis.
In in vitro studies, regadenoson has been shown to have little binding affinity for the A2B and A3 adenosine receptors.
Despite very low binding affinity with the androgen receptor, oxymetholone is highly effective in promoting extensive gains in body mass, mostly by greatly improving protein synthesis.
It also blocks α2c-adrenergic receptors andα2a-adrenergic receptors with a binding affinity of 10.8 and 40.7 nM respectively.
Dianabol has a similarly low binding affinity, and also produces a very good anabolic response.
RuBisCO, the enzyme that captures carbon dioxide in the light-independent reactions,has a binding affinity for both carbon dioxide and oxygen.
Interferon beta-1b both decreases the binding affinity and enhances the internalisation and degradation of the interferon-gamma receptor.
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.
In vitro, florbetaben(18F)shows nanomolar binding affinity to synthetic β-amyloid fibrils and to AD brain homogenate.
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 acts similarly to testosterone,although it has a binding affinity for the androgen receptor five times higher to the latter.
Aripiprazole exhibits high binding affinity in vitro for dopamine D2 and D3, serotonin 5-HT1A and 5-HT2A receptors and has moderate affinity for dopamine D4, serotonin 5-HT2C and 5-HT7, alpha-1 adrenergic, and histamine H1 receptors.
Studies have shown that 19-nor anabolic steroids tend to exhibit a binding affinity for the progesterone receptors in the body.
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.
All anabolic steroids can help improve the metabolic rate, butthose with a strong androgen binding affinity can have an impact on direct lipolysis.
Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for muscarinic receptors.
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.
This psychoactivity occurs because of THC's binding affinity with the CB1 receptors, found mostly in the brain and central nervous system.
Relative binding affinity of anabolic-androgenic steroids: comparison of the binding to the androgen receptors in skeletal muscle and in prostate, as well as to sex hormone-binding globulin”. Endocrinology. 114(6): 2100- 6.
It is of note, however,that this steroid displays significant binding affinity for the progesterone receptor(slightly stronger than progesterone itself).
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.
The avidity of the antibody depends on the affinities of theindividual antibody binding sites, but is greater than the binding affinity as all the antibody-antigen interactions must be broken simultaneously for the antibody to dissociate completely.
This steroid displays significant binding affinity for the progesterone receptor(slightly stronger than progesterone itself).
Dimethyl fumarate does not show any binding affinity to serum proteins which may further contribute to its rapid elimination from the circulation.