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Exact(21)
The predicted and experimental activities of these compounds were well correlated.
As a result, seven compounds were well separated in less than 2 min.
All the synthesized compounds were well characterized by IR, 1H and 13C NMR spectroscopic techniques.
The HOMO level, LUMO level, and band gap of the model compounds were well correlated with the acceptor strength.
Due to their long alkylester and alkylamine terminal groups the examined compounds were well soluble in organic solvents.
Fluorescence emissions observed from poly ethylene terephthalate) (PET), PTT, PBT, and their model compounds were well correlated with the spacer conformations.
Similar(39)
Representative compounds were well-tolerated by human fibroblasts and by mice during the survival/toxicity studies.
In particular, the biosynthetic pathways of several bioactive compounds were well-represented by 115 H. serrata and 98 P. carinatus unique putative transcripts in our 454-EST datasets, totaling 41 H. serrata- and 44 P. carinatus-related EC numbers associated with the biosynthesis of alkaloids, flavones/flavonoids, phenylpropanoids, terpenoids and steroids (see Additional file 2).
The compounds are well characterized by spectral analysis viz.
These compounds are well characterized by 1H and 13C NMR as well as mass spectrometry.
The synthesized compounds are well characterized by various spectroscopic techniques, and their solid-state photophysical properties were investigated.
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