Sentence examples for much higher potency from inspiring English sources

The inhibitor restrained proliferation of lymphocytes with much higher potency than non-hematopoietic cells.

Also, neuropeptides are released in much lower concentrations than are transmitter substances, although the peptides have a much higher potency.

Analogs with Apa30-NH2 such as MR-326 (N-Me-Tyr1, D-Ala2, Arg29, Apa30-NH2-JI-38), and with Gab30-NH2, as MR-502 (D-Ala2, 5F-Phe6, Ser28, Arg29,Gab30-NH2-JI-38) also exhibited much higher potency than JI-38 upon i.v. administration.

SAR studies of lead GnRH receptor antagonists 2a and 2b reported earlier resulted in the discovery of compound 10b which showed much higher potency (Ki=4.6 nM, compared with 2b, Ki=230 nM) in which the 7-position of the imidazolo[1,2-a]pyrimidone core was substituted with a methyl group, and the ester at the 6-position was replaced by the 3-methoxyphenyl group.

The cost of a gram of pot hasn't changed much in 25 years, but much higher potency at the same price-per-gram means that the cost-per-hour of being stoned has fallen about a quarter of its 1992 level; a stoned hour now costs a user who hasn't built a tolerance something less than a dollar.

The muscarinic receptor agonist, carbachol, caused a similar reduction in contractility to that observed with TC but with much higher potency (Fig. 4b).

Although compounds 5 9 are simple and small molecular weight antagonists, they showed much high potency and selectivity than the corresponding compounds having α 2-6Gal linkage.

We have also demonstrated that 6S exhibits much higher antiproliferative potency than that of [6]-gingerol against human lung and colon cancer cells.

The heroin you will get from the doctor will have a much higher purity and potency than the heroin being used by street-addicts, who have to buy from criminals who adulterate it.

In our in vivo studies, T-SN38 conjugates had well targeting ability for tumor tissue and all three of them had much higher anti-ovarian cancer potency than trastuzumab.

Since other synthetic dihydroseselin derivatives with different substituents or without any substituents are inactive or are active only at much higher concentration, the antiviral potency of 16 could be associated with the camphanoyl moieties of its structure.