يعرض 1 - 6 نتائج من 6 نتيجة بحث عن '"Bloomfield, G. C."', وقت الاستعلام: 1.10s تنقيح النتائج
  1. 1
    دورية
    Nonpeptide Bradykinin B2 Receptor Antagonists:  Conversion of Rodent-Selective Bradyzide Analogues into Potent, Orally-Active Human Bradykinin B2 Receptor Antagonists1

    المؤلفون: Dziadulewicz, E. K., Ritchie, T. J., Hallett, A., Snell, C. R., Davies, J. W., Wrigglesworth, R., Dunstan, A. R., Bloomfield, G. C., Drake, G. S., McIntyre, P., Brown, M. C., Burgess, G. M., Lee, W., Davis, C., Yaqoob, M., Phagoo, S. B., Phillips, E., Perkins, M. N., Campbell, E. A., Davis, A. J., Rang, H. P.

    المصدر: Journal of Medicinal Chemistry; May 2002, Vol. 45 Issue: 11 p2160-2172, 13p

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  2. 2
    دورية
    Potent and Orally Bioavailable Non-Peptide Antagonists at the Human Bradykinin B1 Receptor Based on a 2-Alkylamino-5-sulfamoylbenzamide Core

    المؤلفون: Ritchie, T. J., Dziadulewicz, E. K., Culshaw, A. J., Muller, W., Burgess, G. M., Bloomfield, G. C., Drake, G. S., Dunstan, A. R., Beattie, D., Hughes, G. A., Ganju, P., McIntyre, P., Bevan, S. J., Davis, C., Yaqoob, M.

    المصدر: Journal of Medicinal Chemistry; September 2004, Vol. 47 Issue: 19 p4642-4644, 3p

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  3. 3
    دورية
    1-(2-Nitrophenyl)thiosemicarbazides:  A Novel Class of Potent, Orally Active Non-Peptide Antagonist for the Bradykinin B2 Receptor

    المؤلفون: Dziadulewicz, E. K., Ritchie, T. J., Hallett, A., Snell, C. R., Ko, S. Y., Wrigglesworth, R., Hughes, G. A., Dunstan, A. R., Bloomfield, G. C., Drake, G. S., Brown, M. C., Lee, W., Burgess, G. M., Davis, C., Yaqoob, M., Perkins, M. N., Campbell, E. A., Davis, A. J., Rang, H. P.

    المصدر: Journal of Medicinal Chemistry; March 9, 2000, Vol. 43 Issue: 5 p769-771, 3p

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  4. 4
    دورية أكاديمية
    ChemInform Abstract: The Stereoselective Synthesis of 2,9,10-Trioxatricyclo(4.3.1.03,8) decane Analogues of Resiniferatoxin.

    المؤلفون: BLOOMFIELD, G. C., WRIGGLESWORTH, R., RITCHIE, T. J.

    المصدر: ChemInform; Oct1991, Vol. 22 Issue 41, pno-no, 1p

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  5. 5
    دورية أكاديمية
    ChemInform Abstract: Synthesis of 2,9,10-Trioxatricyclo(4.3.1.03,8)decane Analogues of Resiniferatoxin.

    المؤلفون: BLOOMFIELD, G. C., RITCHIE, T. J., WRIGGLESWORTH, R.

    المصدر: ChemInform; Sep1992, Vol. 23 Issue 35, pno-no, 1p

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  6. 6
    دورية أكاديمية
    Bradyzide, a potent non-peptide B(2) bradykinin receptor antagonist with long-lasting oral activity in animal models of inflammatory hyperalgesia.

    المؤلفون: Burgess GM; Novartis Institute for Medical Sciences, 5 Gower Place, London, UK., Perkins MN, Rang HP, Campbell EA, Brown MC, McIntyre P, Urban L, Dziadulewicz EK, Ritchie TJ, Hallett A, Snell CR, Wrigglesworth R, Lee W, Davis C, Phagoo SB, Davis AJ, Phillips E, Drake GS, Hughes GA, Dunstan A, Bloomfield GC

    المصدر: British journal of pharmacology [Br J Pharmacol] 2000 Jan; Vol. 129 (1), pp. 77-86.

    نوع المنشور: Journal Article

    بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 7502536 Publication Model: Print Cited Medium: Print ISSN: 0007-1188 (Print) Linking ISSN: 00071188 NLM ISO Abbreviation: Br J Pharmacol Subsets: MEDLINE

    مواضيع طبية MeSH: Bradykinin Receptor Antagonists*, Anti-Inflammatory Agents, Non-Steroidal/*pharmacology , Hyperalgesia/*drug therapy , Inflammation/*complications , Pyrrolidines/*pharmacology , Thiosemicarbazones/*pharmacology, Administration, Oral ; Animals ; Anti-Inflammatory Agents, Non-Steroidal/administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal/metabolism ; Arthritis, Experimental/complications ; Arthritis, Experimental/drug therapy ; COS Cells ; Calcium/metabolism ; Enzyme Activation/drug effects ; Female ; Humans ; Hyperalgesia/etiology ; In Vitro Techniques ; Membranes/drug effects ; Membranes/metabolism ; Pregnancy ; Pyrrolidines/administration & dosage ; Pyrrolidines/metabolism ; Rats ; Receptor, Bradykinin B1 ; Receptor, Bradykinin B2 ; Receptors, Bradykinin/biosynthesis ; Receptors, Bradykinin/drug effects ; Receptors, Bradykinin/metabolism ; Thiosemicarbazones/administration & dosage ; Thiosemicarbazones/metabolism ; Tumor Cells, Cultured ; Type C Phospholipases/metabolism ; Uterus/drug effects

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