Examples of using Binding affinity in English and their translations into German
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Political
Increasing binding affinity to the GHRH receptors.
Lurasidone also exhibits partial agonism at the 5HT-1A receptor with a binding affinity of 6.38 nM.
Binding affinity for fucose in all binding positions α1-2, α1-3, α1-4 and α1-6.
The detection techniqueis based on the interaction of molecules with high binding affinity to the haptens e.
This steroid has a binding affinity for androgen receptor that's 5 times the 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 a binding affinity to the androgen receptor five times greater than that of testosterone.
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.
Trenbolone compounds have a binding affinity for the androgen receptor five times as high as that of testosterone.
Trenbolone acetate can be injected once a week, also trenbolone acetate is often refined to as"Fina" by user,tren compounds have a binding affinity for the androgen receptor five times as high as that of test.
Being able to assess this binding affinity reliably is the basis for a drug's effectiveness and is enormously important for biotechnology and pharmacology.
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.
Aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for cholinergic muscarinic 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.
Trenbolone in particular possesses very strong binding affinity(much stronger than Nandrolone) for the Progesterone receptor 1.
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.
Trenbolone's strong binding affinity to the androgen has been directly linked to strong lipolysis, enhancing the body's metabolism more than testosterone and burning fat at a higher rate.
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.
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.
Despite quite low binding affinity with the androgen receptor, oxymetholone is extremely reliable in ensuring substantial gains in body mass, mostly by considerably improving healthy protein synthesis.
Despite very low binding affinity with the androgen receptor, oxymetholone is extremely reliable in ensuring considerable gains in body mass, mostly by considerably improving protein synthesis.
Despite extremely reduced binding affinity with the androgen receptor, oxymetholone is very effective in advertising extensive gains in body mass, primarily by substantially improving healthy protein synthesis.
In spite of quite reduced binding affinity with the androgen receptor, oxymetholone is extremely reliable in promoting extensive gains in body mass, mostly by greatly enhancing healthy protein synthesis.
In spite of really reduced binding affinity with the androgen receptor, oxymetholone is very efficient in advertising considerable gains in body mass, mainly by significantly boosting healthy protein synthesis.
In spite of extremely reduced binding affinity with the androgen receptor, oxymetholone is very effective in advertising extensive gains in body mass, mostly by significantly enhancing healthy protein synthesis.
Regardless of extremely reduced binding affinity with the androgen receptor, oxymetholone is very efficient in ensuring extensive gains in body mass, mainly by greatly improving healthy protein synthesis.
Regardless of extremely reduced binding affinity with the androgen receptor, oxymetholone is extremely effective in advertising considerable gains in body mass, mainly by greatly boosting protein synthesis.
Regardless of really reduced binding affinity with the androgen receptor, oxymetholone is highly efficient in promoting substantial gains in body mass, mainly by significantly improving protein synthesis.
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.
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.