, 1997), which were used as the dependent variables of the structural parameters. The aim of this study was to demonstrate the characteristics of both common and differentiating the analyzed compounds in terms of physicochemical and pharmacological effects. Experimental procedure Molecules The following compounds were selected for testing according to reference (Timmermans et al., 1984): α-adrenergic antagonists (AN): prazosin, phentolamine, dihydroergotamine, clozapine, corynanthine, azapetine, yohimbine, piperoxan,
tolazoline, mianserin, rauwolscine; MK-4827 research buy α-adrenergic agonists (AG): lofexidine, clonidine, naphazoline, tiamenidine, xylazine, tramazoline, xylometazoline, tetryzoline, methoxamine, phenylephrine, amidephrine, cirazoline, guanabenz, oxymetazoline, and eight compounds of an experimental click here structures, marked as symbols: DPI, Sgd 101/75, DP-5-ADTN, DP-7-ADTN, DP-5,6-ADTN, DP-6,7-ADTN, St 587, and M-7 (Fig. 1). Repotrectinib mouse Fig. 1 Structural formulas of compounds studied Biological activity data The study used the literature-quoted data of biological activity (Timmermans et al., 1984), are presented in Table 1S. The activity of α-adrenergic agonists—antihypertensive
activity was derived from the stimulation of central α2-adrenoceptors, pC25. The authors expressed data for pC25 in μmol/kg. The values of pC25 were available for lofexidine, clonidine, naphazoline, tiamenidine, xylazine, tramazoline, xylometazoline, and tetryzoline. For the α-adrenergic, antagonists were used: antagonistic activity against phenylephrine induced via α1-adrenoceptors vasoconstriction in rats, pA2 post (α1)—in vivo, antagonistic Terminal deoxynucleotidyl transferase activity of phenylephrine- or norepinephrine-induced stenosis of isolated rabbit pulmonary artery through α1-adrenereceptors post, pA2 post (α1)—in vitro. Activities expressed as pA2 were derived from the equation (Timmermans et al., 1984): $$\textpA_2 = \log \left( \textdose\;\textratio – 1 \right) – \log (\textantagonist\;\textconcentration)$$ (1) Chromatographic and lipophilicity data The values of the logarithm of partition coefficient, log P, were derived from the paper by Timmermans et al. (1984), and they are refer to compounds: lofexidine, clonidine, naphazoline,
tiamenidine, xylazine, tramazoline, xylometazoline, tetryzoline, cirazoline, St-587, and oxymetazoline (Table 2S). Chromatographic data were derived from the article by Nasal et al. (1997), and they are refer to compounds: lofexidine, clonidine, naphazoline, tiamenidine, xylometazoline, tetryzoline, cirazoline, oxymetazoline, prazosin, phentolamine, and tolazoline (Table 2S). These are the values of the logarithms of retention factors determined on Chiral AGP (log k AGP), immobilized artificial membranes IAM.PC.MG (log K IAM) and also the logarithm values of lipophilicity coefficients determined by the policratic method on Suplex pKb-100, pH 7.4 (log k w7.4Su), Spheri RP-18, pH 2.5 (log k w2.5Sp), and Aluspher RP select B, pH 7.3 (log k w7.3Al).