Sentence examples for moieties leads to from inspiring English sources

Exchange of the coordinating solvents molecules in complex 1 to thiocyanate moieties leads to formation of complex 2 ([C40H56N14Ni(NCS)2](CHCl 3) with an extended parameter D/kB = 8.80 K.

Introduction of sulpho-group between the quinoneimine and aryl moieties leads to a considerable increase of electronacceptor properties of compounds under investigation and to decrease of their reduction products nucleophilicity.

Consequently, the reaction of AGT-fusion proteins with O 6-BGnzylguanine (BG) derivatives harboring functional moieties leads to the irreversible and covalent labeling of the fusion proteins since the functional moieties on BG are transferred along with the benzyl group of BG to the reactive Cys, creating a stable thioether covalent bond.

For instance, magnetic nanoparticles chemically modified with chemical functional groups or moieties (e.g., ligand and receptor) have been utilized for high-resolution MRI, which is useful in cancer diagnostics since the chemical modification using chemical functional groups or moieties leads to improved targetability and imaging contrasts [3, 6, 7].

The various levels of analysis indicate that indeed the hybrid linking of naphthoquinone and tryptophan moieties leads to a highly potent inhibitor of both the oligomerization and fibrillization of Aβ with a high affinity of 90 nM and an IC50 of 50 nM, which is markedly lower than that reported for other aromatic Aβ inhibitors (Table S6, Supp. references S1).

If D/G ratio was defined as the ratio of the integrated peak area of D bands divided by the integrated peak area of G bands, it could be found that the larger D/G ratio for SWCNT-PCn and SWCNT-PC (from 3.38 of SWCNT-PCn to 1.07 of SWCNT-PC and to 0.78 of SWCNT) implies that the reaction with phosphoryl choline moieties leads to a higher level of functionalization.

Introduction of a spiro group into the structure of the anthracene moieties lead to a reduction in crystallization tendency, and a high glass transition temperature was observed.

Interestingly, the potency against Escherichia coli strains was unaffected, whereas modification with hydrophobic moieties led to increased activity towards the Gram-negative Acinetobacter baumannii.

Introduction of a spiro group into the anthracene moieties lead to a reduction in crystallization tendency, and a high glass transition temperature was observed.

The appropriate exploration of the position C-6 with a combination of H-bond acceptor groups coupled with bulky/lipophilic moieties led to the discovery of a new series of mGluR1 antagonists.

Modification of the ester and amino acid moieties lead to a compound INX-08189 that exhibits 10 nM potency in the HCV genotype 1b subgenomic replicon, thus being 500 times more potent than the parent nucleoside.