Sentence examples for between these two compounds from inspiring English sources

The peak shifts at 1092 and 1744 cm−1 confirmed the presence of molecular interactions between these two compounds.

Moreover, we analysed the possible reactions which may occur between these two compounds and their by-products outside and inside our body.

However, a major difference between these two compounds was observed as the oxidation of a methyl and a methylene in 3α-deacetyl-amoorastatin core to an oxymethylene (δC 71.92, δH 3.60, 3.89 (each 1H, d, J = 10.7 Hz) and an oxymethine [δC 68.60, δH 4.54 (dd, J = 4.4, 3.4 Hz] in 1, respectively.

The only difference between these two compounds was that the oxygenated methine (C-12) at δC 72.3 in (3β,12α -3,12-dihydroxyisopimara-7,15-dien-2-one [8] shifted downfield to δC 74.6 in 4, and concurrent chemical shift changes of those carbons surrounding C-12 also occurred.

The structural difference between these two compounds is the phenolic group in thymol as compared to menthol that only has the hydroxyl group; p-Cymene has the benzene group without hydroxyl group with an activity of 24.0 μg/mL; this demonstrate the importance of the phenolic group in the larvicidal activity.

Objectives: Neopterin and homocysteine promote vascular smooth muscle cell proliferation through the activation of nuclear factorκ B. The aim of this study was to investigate the relation between these two compounds in healthy subjects by a rapid HPLC-fluorometric method which simplifies sample pretreatment for the measurement of neopterin in serum.

For each type of cancer, we divided this compound list into two parts: FDA approved and routinely used drugs (the Successful drug list) and the remainder (the Candidate list), and tested whether we could statistically discriminate between these two compound lists using the perturbation index.

The direction of some of these associations was surprisingly different between these two compound classes.

No correlation between the sensitivity to these two compounds was observed.

Although the dispersion of experimental data yields non-significant differences between values obtained for these two compounds, the mean values point to a slightly more potent inhibitory effect of octahydrohyperforin.

In spite of the similarities, ivermectin is regarded as the least lipophilic of the macrocyclic lactone antiparasitics [ 17], which probably causes differences between the pharmacokinetics of these two compounds.