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9 out of 12 of the tested compounds displayed affinity at the α1A and α1D -AR subtypes and 6 displayed affinity at all three α1-AR subtypes, no α1B-AR selective compounds were identified.
Glycopeptides 4 and 7 are Aq-specific, i.e. they both displayed affinity for Aq but bound poorly to DR4.
9 of the 12 isolated compounds displayed affinity at the α1A and α1D -AR subtypes, and all compounds with α1-AR affinity displayed negative efficacy.
Several of these domains, including DBL5ε, have, to some extent, displayed affinity for CSA in vitro [12], [13], [14], [15] [16].
With the exception of compounds 4, 5 and 10, all compounds displayed affinity for the α1-ARs in the micromolar range (Table 1).
PaLPMO9H displayed affinity for non-cellulosic substrates including XG, β-glucans, and glucomannan.
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Some synthesized compounds, tested in binding assays for the human cloned α1A-, α1B-, and α1D-AR subtypes, displayed affinities in the nanomolar range.
A false-color matrix of vector correlations displayed affinities among species consistent with higher-order taxonomy.
Quite a few King's Hall soulies were obviously wearing clothes from decades earlier, complete with patches displaying affinity to the Torch or other clubs.
Herpes simplex viruses (HSVs) display affinity for cell-surface heparan sulfate proteoglycans with biological relevance in virus entry.
Dihydroergotamine (DHE) is an acute antimigraine agent that displays affinity for dopamine D2-like receptors, serotonin 5-HT1/2 receptors and α1/α2-adrenoceptors.
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CEO of Professional Science Editing for Scientists @ prosciediting.com