ANIMAL CELL;
ANIMAL EXPERIMENT;
ANIMAL TISSUE;
ARTICLE;
BINDING AFFINITY;
CONTROLLED STUDY;
DRUG ANTAGONISM;
DRUG POTENCY;
DRUG SCREENING;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENANTIOMER;
GUINEA PIG;
HUMAN;
MALE;
NONHUMAN;
RAT;
IV. International union of pharmacology nomenclature of adrenoceptors
Bylund D.B., Eikenburg D.C., Hieble J.P., Langer S.Z., Lefkowitz R.J., Minneman K.P., Molinoff P.B., Ruffolo R.R. Jr., Trendelenburg U. IV. International union of pharmacology nomenclature of adrenoceptors. Pharmacol. Rev. 46:1994;121-136.
Structure-activity relationships in prazosin-related compounds. 2. Role of the piperazine ring on α-blocking activity
Giardinà D., Crucianelli M., Romanelli R., Leonardi A., Poggesi E., Melchiorre C. Structure-activity relationships in prazosin-related compounds. 2. Role of the piperazine ring on α-blocking activity. J. Med. Chem. 39:1996;4602-4607.
1B-adrenergic receptor for improvement of sexual dysfunction, US Patent 6,303,606 Bl, 16 October, 2001
1B-adrenergic receptor for improvement of sexual dysfunction, US Patent 6,303,606 Bl, 16 October, 2001.
17
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Quinoxaline studies. XII. Stereodirective syntheses of cis- and trans-decahydroquinoxalines and cis- and trans-decahydroquinoxa-lones-2
Brill E., Schultz H.P. Quinoxaline studies. XII. Stereodirective syntheses of cis- and trans-decahydroquinoxalines and cis- and trans-decahydroquinoxa-lones-2. J. Org. Chem. 29:1964;211-220.
Cumulative dose-response curves. II. Technique for the making of dose-response curves in isolated organs and the evaluation of drug parameters
Van Rossum J.M. Cumulative dose-response curves. II. Technique for the making of dose-response curves in isolated organs and the evaluation of drug parameters. Arch. Int. Pharmacodyn. 143:1963;299-330.
F.E. King, M.F. Grundon, The constitution of chlorophorin. Part II. Further oxidation experiments, and the completion of the structural problem, J. Chem. Soc. (1950) 3547-3551
F.E. King, M.F. Grundon, The constitution of chlorophorin. Part II. Further oxidation experiments, and the completion of the structural problem, J. Chem. Soc. (1950) 3547-3551.
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Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-Aryl and C(6)-substituents
Young J.R., Huang S.X., Chen I., Walsh T.F., DeVita R.J., Wyvratt M.J. Jr., Goulet M.T., Ren N., Lo J., Yang Y.T., Yudkovitz J.B., Cheng K., Smith R.G. Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-Aryl and C(6)-substituents. Bioorg. Med. Chem. Lett. 10:2000;1723-1727.
α-adrenoceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on α-adrenoceptor activity
Chapleo C.B., Myers P.L., Butler R.C., Davis J.A., Doxey J.C., Higgins S.D., Myers M., Roach A.G., Smith C.F., Stillings M.R., Welbourn A.P. α-adrenoceptor reagents. 2. Effects of modification of the 1,4-benzodioxan ring system on α-adrenoceptor activity. J. Med. Chem. 27:1984;570-576.
Simultaneous analysis of families of sigmoidal curves: Application to bioassay, radioligand assay, and physiological dose-response curves
De Lean A., Munson P.J., Rodbard D. Simultaneous analysis of families of sigmoidal curves: application to bioassay, radioligand assay, and physiological dose-response curves. Am. J. Physiol. 235:1978;E97-E102.