يعرض 1 - 9 نتائج من 9 نتيجة بحث عن '"Harrell, C. M."', وقت الاستعلام: 1.38s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Ferritin mRNA: Interactions of Iron Regulatory Element with Translational Regulator Protein P-90 and the Effect on Base-Paired Flanking Regions

    المؤلفون: Harrell, C. M., McKenzie, A. R., Patino, M. M., Walden, W. E., Theil, E. C.

    المصدر: Proceedings of the National Academy of Sciences of the United States of America, 1991 May . 88(10), 4166-4170.

    URL الوصول: https://www.jstor.org/stable/2357004

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  2. 2
    دورية
    2,3-Diaminopyridine Bradykinin B1 Receptor Antagonists

    المؤلفون: Kuduk, S. D., Ng, C., Feng, D.-M., Wai, J. M.-C., Chang, R. S. L., Harrell, C. M., Murphy, K. L., Ransom, R. W., Reiss, D., Ivarsson, M., Mason, G., Boyce, S., Tang, C., Prueksaritanont, T., Freidinger, R. M., Pettibone, D. J., Bock, M. G.

    المصدر: Journal of Medicinal Chemistry; December 2004, Vol. 47 Issue: 26 p6439-6442, 4p

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  3. 3
    دورية
    Benzodiazepines as Potent and Selective Bradykinin B1 Antagonists

    المؤلفون: Wood, M. R., Kim, J. J., Han, W., Dorsey, B. D., Homnick, C. F., DiPardo, R. M., Kuduk, S. D., MacNeil, T., Murphy, K. L., Lis, E. V., Ransom, R. W., Stump, G. L., Lynch, J. J., O'Malley, S. S., Miller, P. J., Chen, T.-B., Harrell, C. M., Chang, R. S. L., Sandhu, P., Ellis, J. D., Bondiskey, P. J., Pettibone, D. J., Freidinger, R. M., Bock, M. G.

    المصدر: Journal of Medicinal Chemistry; May 2003, Vol. 46 Issue: 10 p1803-1806, 4p

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  4. 4
    دورية
    Design and Synthesis of Novel α1a Adrenoceptor-Selective Antagonists. 1. Structure−Activity Relationship in Dihydropyrimidinones

    المؤلفون: Nagarathnam, D., Miao, S. W., Lagu, B., Chiu, G., Fang, J., Dhar, T. G. Murali, Zhang, J., Tyagarajan, S., Marzabadi, M. R., Zhang, F., Wong, W. C., Sun, W., Tian, D., Wetzel, J. M., Forray, C., Chang, R. S. L., Broten, T. P., Ransom, R. W., Schorn, T. W., Chen, T. B., O'Malley, S., Kling, P., Schneck, K., Bendesky, R., Harrell, C. M., Vyas, K. P., Gluchowski, C.

    المصدر: Journal of Medicinal Chemistry; November 18, 1999, Vol. 42 Issue: 23 p4764-4777, 14p

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  5. 5
    دورية
    Design and Synthesis of Novel α1a Adrenoceptor-Selective Antagonists. 2. Approaches To Eliminate Opioid Agonist Metabolites via Modification of Linker and 4-Methoxycarbonyl-4-phenylpiperidine Moiety1,2

    المؤلفون: Dhar, T. G. Murali, Nagarathnam, D., Marzabadi, M. R., Lagu, B., Wong, W. C., Chiu, G., Tyagarajan, S., Miao, S. W., Zhang, F., Sun, W., Tian, D., Shen, Q., Zhang, J., Wetzel, J. M., Forray, C., Chang, R. S. L., Broten, T. P., Schorn, T. W., Chen, T. B., O'Malley, S., Ransom, R., Schneck, K., Bendesky, R., Harrell, C. M., Vyas, K. P., Zhang, K., Gilbert, J., Pettibone, D. J., Patane, M. A., Bock, M. G., Freidinger, R. M., Gluchowski, C.

    المصدر: Journal of Medicinal Chemistry; November 18, 1999, Vol. 42 Issue: 23 p4778-4793, 16p

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  6. 6
    دورية
    Characterization of the Human Oxytocin Receptor Stably Expressed in 293 Human Embryonic Kidney Cells

    المؤلفون: Jasper, J. R., Harrell, C. M., O'Brien, J. A.

    المصدر: Life Sciences; 1995, Vol. 57 Issue: 24 p2253-2253, 1p

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  7. 7
    دورية أكاديمية
    Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 1. Structure-activity relationship in dihydropyrimidinones.

    المؤلفون: Nagarathnam D; Departments of Chemistry and Pharmacology, Synaptic Pharmaceutical Corporation, Paramus, NJ 07652, USA., Miao SW, Lagu B, Chiu G, Fang J, Murali Dhar TG, Zhang J, Tyagarajan S, Marzabadi MR, Zhang F, Wong WC, Sun W, Tian D, Wetzel JM, Forray C, Chang RS, Broten TP, Ransom RW, Schorn TW, Chen TB, O'Malley S, Kling P, Schneck K, Bendesky R, Harrell CM, et. al.

    المصدر: Journal of medicinal chemistry [J Med Chem] 1999 Nov 18; Vol. 42 (23), pp. 4764-77.

    نوع المنشور: Journal Article

    بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 9716531 Publication Model: Print Cited Medium: Print ISSN: 0022-2623 (Print) Linking ISSN: 00222623 NLM ISO Abbreviation: J Med Chem Subsets: MEDLINE

    مواضيع طبية MeSH: Adrenergic alpha-1 Receptor Antagonists*, Adrenergic alpha-Antagonists/*chemical synthesis , Pyrimidinones/*chemical synthesis, Adrenergic alpha-Antagonists/chemistry ; Adrenergic alpha-Antagonists/metabolism ; Adrenergic alpha-Antagonists/pharmacology ; Animals ; Binding, Competitive ; Blood Pressure/drug effects ; Dogs ; Drug Design ; Drug Evaluation, Preclinical ; Humans ; In Vitro Techniques ; Male ; Prostate/metabolism ; Pyrimidinones/chemistry ; Pyrimidinones/metabolism ; Pyrimidinones/pharmacology ; Radioligand Assay ; Rats ; Rats, Sprague-Dawley ; Receptors, Adrenergic, alpha-1/metabolism ; Stereoisomerism ; Urethra/drug effects ; Urethra/physiology

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  8. 8
    دورية أكاديمية
    Design and synthesis of novel alpha(1)(a) adrenoceptor-selective antagonists. 2. Approaches to eliminate opioid agonist metabolites via modification of linker and 4-methoxycarbonyl-4-phenylpiperidine moiety.

    المؤلفون: Murali Dhar TG; Departments of Chemistry and Pharmacology, Synaptic Pharmaceutical Corporation, Paramus, NJ 07652, USA., Nagarathnam D, Marzabadi MR, Lagu B, Wong WC, Chiu G, Tyagarajan S, Miao SW, Zhang F, Sun W, Tian D, Shen Q, Zhang J, Wetzel JM, Forray C, Chang RS, Broten TP, Schorn TW, Chen TB, O'Malley S, Ransom R, Schneck K, Bendesky R, Harrell CM, Vyas KP, et. al.

    المصدر: Journal of medicinal chemistry [J Med Chem] 1999 Nov 18; Vol. 42 (23), pp. 4778-93.

    نوع المنشور: Journal Article

    بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 9716531 Publication Model: Print Cited Medium: Print ISSN: 0022-2623 (Print) Linking ISSN: 00222623 NLM ISO Abbreviation: J Med Chem Subsets: MEDLINE

    مواضيع طبية MeSH: Adrenergic alpha-1 Receptor Antagonists*, Adrenergic alpha-Antagonists/*chemical synthesis , Piperidines/*chemical synthesis , Pyrimidinones/*chemical synthesis, Adrenergic alpha-Antagonists/chemistry ; Adrenergic alpha-Antagonists/metabolism ; Adrenergic alpha-Antagonists/pharmacology ; Animals ; Biological Availability ; Blood Pressure/drug effects ; Dogs ; Drug Design ; Drug Evaluation, Preclinical ; GTP-Binding Proteins/metabolism ; Half-Life ; Humans ; In Vitro Techniques ; Male ; Microsomes/metabolism ; Piperidines/chemistry ; Piperidines/metabolism ; Piperidines/pharmacology ; Prostate/metabolism ; Pyrimidinones/chemistry ; Pyrimidinones/metabolism ; Pyrimidinones/pharmacology ; Rats ; Rats, Sprague-Dawley ; Receptors, Adrenergic, alpha-1/metabolism ; Receptors, Opioid, mu/agonists ; Recombinant Proteins/metabolism ; Stereoisomerism ; Structure-Activity Relationship ; Urethra/drug effects ; Urethra/physiology

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  9. 9
    دورية أكاديمية
    Progress in the development of oxytocin antagonists for use in preterm labor.

    المؤلفون: Pettibone DJ; Department of New Lead Pharmacology, Merck Research Laboratories, West Point, PA 19486, USA., Guidotti M, Harrell CM, Jasper JR, Lis EV, O'Brien JA, Reiss DR, Woyden CJ, Bock MG, Evans BE, et. al.

    المصدر: Advances in experimental medicine and biology [Adv Exp Med Biol] 1995; Vol. 395, pp. 601-12.

    نوع المنشور: Journal Article; Review

    بيانات الدورية: Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 0121103 Publication Model: Print Cited Medium: Print ISSN: 0065-2598 (Print) Linking ISSN: 00652598 NLM ISO Abbreviation: Adv Exp Med Biol Subsets: MEDLINE

    مواضيع طبية MeSH: Hormone Antagonists/*therapeutic use , Obstetric Labor, Premature/*drug therapy , Oxytocin/*antagonists & inhibitors , Tocolytic Agents/*therapeutic use, Animals ; Benzoxazines ; Camphanes/administration & dosage ; Camphanes/chemistry ; Camphanes/therapeutic use ; Dogs ; Female ; Hormone Antagonists/administration & dosage ; Hormone Antagonists/chemistry ; Humans ; In Vitro Techniques ; Macaca mulatta ; Molecular Structure ; Obstetric Labor, Premature/physiopathology ; Oxazines/chemistry ; Oxazines/therapeutic use ; Pan troglodytes ; Piperazines/administration & dosage ; Piperazines/chemistry ; Piperazines/therapeutic use ; Piperidines/chemistry ; Piperidines/therapeutic use ; Pregnancy ; Rats ; Tocolytic Agents/administration & dosage ; Tocolytic Agents/chemistry ; Uterine Contraction/drug effects

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