ANTIARRHYTHMIC ACTIVITY;
ARTICLE;
CANCER THERAPY;
CELL PROLIFERATION;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG INHIBITION;
DRUG STRUCTURE;
DRUG SYNTHESIS;
MULTIDRUG RESISTANCE;
NONHUMAN;
AMIDINES;
ANIMALS;
ANTI-ARRHYTHMIA AGENTS;
ANTINEOPLASTIC AGENTS;
ARRHYTHMIAS, CARDIAC;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DOSE-RESPONSE RELATIONSHIP, DRUG;
DRUG DESIGN;
DRUG RESISTANCE, MULTIPLE;
DRUG RESISTANCE, NEOPLASM;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
ISOQUINOLINES;
MICE;
MICE, NUDE;
MYOCARDIAL CONTRACTION;
NEOPLASMS;
RATS;
RATS, SPRAGUE-DAWLEY;
STRUCTURE-ACTIVITY RELATIONSHIP;
TETRAHYDROISOQUINOLINES;
TIME FACTORS;
VERAPAMIL;
7/ml. When the tumors reached a mean diameter of 0.4-0.6 cm, the animals were randomized into groups of ten and treated with drugs in the intravenous injection three times a week. Control animals were treated with vehicle alone. Tumor weights were measured. The inhibition ratio (I%) of tumor growth was calculated using ((mean relative tumor weights of the treated group)/(the mean relative tumor weights of ADM group) - 1) × 100 (%).
17
44649158000
note
emission = 535 nm) was measured in a microplate spectrofluorometer. Assays were performed in triplication. The inhibitory ratio (I%) was calculated using ((mean absolute fluorescence value of the treated group - the mean absolute fluorescence value of control)/the mean absolute fluorescence value of control) × 100 (%), where absolute fluorescence value for (fluorescence value of each well) - (the bases of fluorescence value of 96-well plate).
18
0028229150
Schinkel A.H., Smit J.J.M., Tellingem O., Beijnen J.H., Wagenaar R., Demter L., Mol C.A.A.M., Valk M.A., Maandag-Robanu E.C., Riele H.P.J., Berns A.J.M., and Borst P. Cell 77 (1994) 491
emission = 535 nm) was measured in a microplate spectrofluorometer. The content of protein was measured using the method of Coomassie brilliant blue for fluorescence intensity value. Assays were performed in duplicate, with at least three separate experiments.
23
44649172788
note
emission = 535 nm) was measured in a microplate spectrofluorometer. The content of protein was measured using the method of Coomassie brilliant blue for fluorescence intensity value. Assays were performed in duplicate, with at least three separate experiments.
24
0026725230
Seydel J.K., Velasco M.A., Coats E.A., Cordes H.P., Kunz B., and Wiese M. Quant. Struct.-Act. Relat. 11 (1992) 205
HH are fluorescence intensity value when excitation in horizontal direction. Assays were performed in duplicate, with at least three separate experiments.
27
44649151450
note
2 (5%). The isometric contractions of the aortic rings were measured with a force-displacement transducer. After 60 min of equilibration, the rings were exposed to 20 mM KCl or 80 mM KCl. When the tension had stabilized, the drugs were added to the bath at increasing concentrations until maximal relaxation. The relaxation response was expressed as the percentage of the contractile response to KCl.
28
44649109884
note
SD rats (2.5-3.5 kg) were anesthetized with urethane (1.2 g/kg ip). The test compounds were dissolved in normal saline and administrated by femoral vein. Intravenous administration of aconitine nitrate (1 μg/0.2 ml/min) was kept constant velocity from femoral vein by peristaltic pump after 2 min.
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