Examples of using Binding affinity in English and their translations into Portuguese
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Increasing binding affinity to the GHRH receptors.
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.
Description: A 60 kDa tetrameric protein that exhibits high binding affinity for biotin.
CJC 1295 increasing binding affinity to the ghrh receptors.
Trenbolone substances posses 5 times the androgen receptor binding affinity of testosterone.
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.
The binding affinity of 4-hydroxymethyl ambrisentan for the human endothelin receptor is 65-fold less than ambrisentan.
Lurasidone also exhibits partial agonism at the 5HT-1A receptor with a binding affinity of 6.38 nM.
Clostebol has a slightly lower binding affinity for the AR than testosterone and no binding to the PR or GR.
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 exceptionally solid binding affinity for the androgen receptor also, even surpassing that of testosterone.
Separation steps usually exploit differences in protein size,physico-chemical properties, binding affinity and biological activity.
Trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.
Ioflupane also binds to the serotonin transporter on 5-HT neurons but with lower(approximately 10-fold) binding affinity.
ITC is particularly useful as it gives not only the binding affinity, but also the thermodynamics of the binding. .
The binding affinity of neuropilin-2 varies for different class 3 semaphorin isoforms and is dependent on the composition of the dimer.
Trenbolone in particular possesses very strong binding affinity(much stronger than Nandrolone) for the Progesterone receptor 1.
For example, it is possible to calculate digitally what changes could improve the drug candidate's binding affinity, i.e.
Trenbolone has a very strong binding affinity for the androgen receptor also, also exceeding that of testosterone.
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.
Interferon beta-1b both decreases the binding affinity and enhances the internalisation and degradation of the interferon-gamma receptor.
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.
All these actions are mediated by FGF23 binding to FGF receptors FGFR and its co-receptor Klotho,which greatly increases the binding affinity of FGF23 for FGFR.
Methyltrienolone has an extremely strong binding affinity for the androgen receptor as well, even surpassing that of testosterone.
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.