Sentence examples for backbone compounds from inspiring English sources

The main-chain degrading PCWDEs participate in breakdown of highly polymeric backbone compounds, such as cutin polymer, (gluco)xylan, pectin or glucan.

In spite of the estrogen backbone compound 21 did not show estrogen receptor mediated effects in vitro or in vivo.

Neither statistically significant enhancement nor decrease of the effect was detected by the PEGylation of the phosphodiester backbone compound.

A genomic analysis led to the identification of genomic loci that suggest a versatile metabolism of terpene-backbone compounds.

At this moment, it is unclear whether all 22 genes from the 28-kb GI are actually necessary for the metabolism of the aliphatic C8-chain of β-myrcene or whether the high expression levels of the island are induced by a chemosensory signal common to a broader metabolic potential toward several terpene-backbone compounds.

For phosphorothioate backbone modified compounds, the transition temperature was about 1 °C higher when the PEG chain was attached.

Interestingly, the same hydrogen-bonding interactions between the backbone of compound 6 and the β5 site are observed, including the presence of the bridging water molecule between the P3 carbonyl group and Ala and Ala.

Chemists use a variety of expressions to create compound class terms from a specific compound name – for example "backbone", "scaffold", "derivative", "compound class" are often used suffixes or "substituted" is a common prefix that generates a class term.

In case of substituents in the meta-position (13 and 15) the compound forms additional water mediated interactions with the protein backbone, but the compounds are in two conformations in the crystal structures indicating that the binding poses would be of similar energy and the contribution of this hydrogen bond is not providing an affinity increase (Fig. 3b and d).

Moreover, the inverted peptide backbone in these compounds is predicted to render them more resistant to degradation than conventional peptidic inhibitors, and they proved useful in downstream cellular assays.

Significantly, the acyclic nature of 45 and 46 and the flexibility of the glycoluril tetramer backbone allow these compounds to flex like a hand to accommodate a wide range of guest sizes.