Sentence examples for moiety when compared from inspiring English sources

Unexpectedly, the two Kunitz domains of boophilin not only diverge largely in three-dimensional structure from ornithodorin, but also occupy significantly different positions relative to the proteinase moiety, when compared to the thrombin·ornithodorin complex (Figure 7A).

Agents from this subclass possess a more flexible dihedral angle between the aniline ring and cyanovinyl moiety when compared with first-generation agents.

The high lipophilicity of this aldehydic moiety when compared to AHC compounds with a less lipophilic pyridoxal or salicylaldehyde group is correlated to increased anti-proliferative effects [ 34] and likely contributes to the effectiveness of the novel HNTMB studied here.

The perturbed chemical shifts along the B helix induced by levosimendan may result from a larger displacement of cTnI144−163 by the voluminous mesoxalonitrile hydrazone moiety when compared with CMDP.

TRAP staining and immunohistochemistry staining of COL I demonstrated lower numbers of osteoclasts and significantly increased numbers of osteoblasts in the bone-targeting moiety delivering pcDNA3.1-Sema3a-GFP group, when compared to the control group (p < 0.01, p < 0.001,respectively).

These differences in quaternary arrangement of Kunitz modules relative to the serine proteinase moiety result in large differences when compared to the thrombin·ornithodorin complex, as we discuss below.

Immunocytokines provide increased half-life to cytokines, but the antibody moiety has a decreased half-life when compared with the non-fused protein.

An additional product containing the oxazoline ring in daunosamine moiety was obtained during the synthesis of formamidinodoxorubicin from DOX. Formamidine derivatives demonstrate better anticancer properties when compared with parental DOX, such as lower cardiotoxicity and comparable or higher antiproliferative activity.

The greater flexibility of the cyclohexylmethyl-piperazine moiety of PBTZ169, making it more adaptable to the active site when compared to BTZ043, might account in part for its higher affinity and faster inactivation of DprE1.

It is also worth noting that the presence of two BP moieties in [Cu dtcbp 2] increases the binding capabilities to these materials when compared to mono-BP compounds, which seem to be selective for HA among the calcium salts.[ 14] [Cu(dtcbp)2], however, binds well to HA, CC, calcium phosphate (CP), and β-tricalcium phosphate (b-CP).

Since the primary structure around the Trp15 (Trp18 in PsTRXh1) changes the most in both proteins (Fig. 1), we suggest that the differences in the chemical-denaturation observed in PsTRXh2, when compared to PsTRXh1, are due to the presence of residual structure around this indole moiety.