Examples of using Binding affinity in English and their translations into Russian
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Increasing binding affinity to the GHRH receptors.
The Mesterolone hormone will also carry a strong binding affinity to the androgen receptor.
This steroid has a binding affinity for androgen receptor that's 5 times the testosterone.
The hormone has also been shown to have an extremely strong binding affinity for the androgen receptor.
Trenbolone has a binding affinity to the androgen receptor five times greater than that of testosterone.
This reflects a 6-10 fold reduction in binding affinity compared to estradiol.
It has a very strong binding affinity to the androgen receptor(A. R), binding much more strongly than testosterone as well as nandrolone.
Each of these receptor types has different binding affinity to certain types of neurotrophins.
They reported that acetylation of Lys5 nearthe N-terminal region and Lys29 in the beta-turn region led to substantial decreases in DTX-I binding affinity.
CJC 1295 increasing binding affinity to the ghrh receptors.
The SP form(the(-) optical isomer) is the more active enantiomer due to its greater binding affinity to acetylcholinesterase.
Trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.
Eph receptors in turn are classified as either EphAs orEphBs based on their binding affinity for either the ephrin-A or ephrin-B ligands.
Clostebol has a slightly lower binding affinity for the AR than testosterone and no binding to the PR or GR. The chlorine atom blocks the action of aromatase on this molecule.
Finally, mutations at key sites in DNA gyrase ortopoisomerase IV can decrease their binding affinity to quinolones, decreasing the drugs' effectiveness.
However, due to its binding affinity to progesterone, Metribolone can still produce undesirable side effects(detailed below), especially when stacked with other estrogen promoting steroids.
This greatly increases the hormones androgen binding affinity and inhibits the hormone from aromatizing.
It's important to remember DHT, the basis of Masteron,is five times more androgenic than testosterone with a much stronger binding affinity to the androgen receptor.
Each type of neurotrophin has different binding affinity toward its corresponding Trk receptor.
Knowledge of the preferred orientation in turn may be used to predict the strength of association or binding affinity between two molecules using, for example.
Methyltrienolone has an extremely strong binding affinity for the androgen receptor as well, even surpassing that of testosterone.
The axons of these proprioceptive sensory neurons are much thicker than those of nociceptive sensory neurons, which express trkA. p75NTR(p75 neurotrophin receptor)affects the binding affinity and specificity of Trk receptor activation by neurotrophins.
This is the direct reason for the increased binding affinity making Trenbolone five times more potent than testosterone.
The end result gives us an anabolic steroid with an androgenic rating of 40-60 with a much lower binding affinity to the androgen receptor compared to testosterone.
Trenbolone also has a very strong binding affinity to the androgen receptor(A. R), binding much more strongly than testosterone(4).
The Trenbolone hormone carries a double bond at carbons 9 and 11, which in turn slows its metabolism,greatly increases its binding affinity to the androgen receptor, and inhibits it from aromatizing.
Depending on this modified state, FOXO4 binding affinity for DNA is altered, allowing for FOXO4 to regulate many cellular pathways including oxidative stress signaling, longevity, insulin signaling, cell cycle progression, and apoptosis.
Data about mutations that decrease protein stability and binding affinity and, respectively, decrease and increase fitness.
Trenbolone acetate can be injected once a week, also trenbolone acetate is often refined to as"Fina" by user,trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.
This method allows the determination of the binding affinity without any limitation to the ligand's molecular weight.