Examples of 'weak inhibitor' in a sentence

Meaning of "weak inhibitor"

A weak inhibitor refers to a substance or drug that has a relatively low binding affinity to its target enzyme or receptor. It has the ability to partially inhibit the activity of the target, but not fully block or deactivate it. Weak inhibitors are often used in research and drug development to study the effects of partial inhibition on biological processes

How to use "weak inhibitor" in a sentence

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weak inhibitor
The remaining amine is still a weak inhibitor.
Lamotrigine is a weak inhibitor of dihydrofolate reductase.
The researchers previously had shown that vitamin K alone is a weak inhibitor of HCC growth.
It is a weak inhibitor of prostaglandin biosynthesis.
Etravirine is also a weak inhibitor of.
It is also only a weak inhibitor of mammalian DNA polymerases alpha and beta.
The smaller protein is a powerful inhibitor of chymotrypsin, and a weak inhibitor of trypsin.
As such, flutamide is a weak inhibitor of androgen biosynthesis.
In vitro and in vivo studies indicate that venlafaxine is a weak inhibitor of CYP2D6.
Ivacaftor is a weak inhibitor of CYP3A when given as monotherapy.
Paliperidone in high concentrations is a weak inhibitor of P-glycoprotein.
Amantadine, a weak inhibitor of the NMDA glutamate receptor, has been tested in autism.
Ivabradine is metabolised by CYP3A4 only and it is a very weak inhibitor of this cytochrome.
Amlodipine is a weak inhibitor of CYP3A and may increase exposure to CYP3A substrates.
Blood or plasma contain antithrombin III, which is a relatively weak inhibitor of thrombin.

See also

Tenofovir diphosphate is a weak inhibitor of cellular polymerases α, β, and γ.
Additionally, a clinical study with ivacaftor monotherapy showed that ivacaftor is a weak inhibitor of P-gp.
Serotonin itself is a weak inhibitor of tyrosinase with 0.11 times the potency of kojic acid.
In vitro studies indicate that lacosamide may be a weak inhibitor and inducer of CYP3A4.
Abacavir is also a weak inhibitor of cellular DNA polymerases ( alpha, beta, and gamma ).
No difference in exposure was found with concomitantly treatment with fluvastatin weak inhibitor of CYP2C9.
Febuxostat was shown to be a weak inhibitor of CYP2D6 in vitro.
A test compound with an IC50 greater than 10 µM is called a weak inhibitor.
Febuxostat was shown to be a weak inhibitor of CYP2C8 in vitro.
TEA is a weak inhibitor of KCNQ1/KvLQT1 whereas clofilium is a strong inhibitor of KCNQ1/KvLQT1.
Effects of celecoxib on other medicinal products Celecoxib is a weak inhibitor of CYP2D6.
Mirabegron is a weak inhibitor of P-gp.
It is a weak inhibitor of CYP3A and P-gp and a potential inhibitor of CYP2C9.
In vivo asenapine appears to be at most a weak inhibitor of CYP2D6.
It is also a weak inhibitor in A / Fe water, or water with dissolved iron.
Telithromycin is an inhibitor of CYP3A4 and a weak inhibitor of CYP2D6.
By contrast, TFPI-2 is a weak inhibitor of factor Xa amidolytic activity.
Medicinal products metabolised by CYP2B6, prasugrel is a weak inhibitor of CYP2B6.
That compound is a weak inhibitor of 4-nitrophenyl acetate cleavage 16 µM ; FIG.
Thus, in vivo, SAPHRIS appears to be at most a weak inhibitor of CYP2D6.
Vorapaxar is a weak inhibitor of the intestinal P-glycoprotein ( P-gp ) transporter.
Prasugrel, Prasugrel is a weak inhibitor of CYP2B6.
Celecoxib is a weak inhibitor of CYP2D6.
Binimetinib is a weak inhibitor of OAT3.
Opicapone is a weak inhibitor of CYP2C8.
Opicapone is a weak inhibitor of OATP1B1.
Asenapine is a weak inhibitor of CYP2D6.
Darunavir is an inhibitor of CYP3A, a weak inhibitor of CYP2D6 and an inhibitor of P-gp.

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Examples of using Weak
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