Search Results - "Hauel, N"
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1
Antithrombotic and anticoagulant effects of the direct thrombin inhibitor dabigatran, and its oral prodrug, dabigatran etexilate, in a rabbit model of venous thrombosis
Published in Journal of thrombosis and haemostasis (01-06-2007)“…Background: Oral anticoagulant therapies targeted at thrombin are being developed to overcome limitations associated with current standard therapies…”
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2
288 EFFECT OF THE B1 ANTAGONIST BI 41488 IN DIFFERENT ANIMAL MODELS OF INFLAMMATORY PAIN
Published in European journal of pain (01-09-2009)Get full text
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3
Pharmacological characterization of the novel nonpeptide angiotensin II receptor antagonist, BIBR 277
Published in British journal of pharmacology (01-09-1993)“…1 The pharmacological profile of BIBR 277, 4′‐[(1,4′‐dimethyl‐2′‐propyl[2,6′‐bi‐1H‐benzimidazol]‐1′‐yl)methyl]‐[1,1′‐biphenyl]‐2‐carboxylic acid, a novel,…”
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4
6-Substituted benzimidazoles as new nonpeptide angiotensin II receptor antagonists: synthesis, biological activity, and structure-activity relationships
Published in Journal of medicinal chemistry (10-12-1993)“…Starting from the recently reported nonpeptidic angiotensin II (AII) receptor antagonists DuP753 (1) and Exp 7711 (2), we have designed and investigated novel…”
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5
Structural Basis for Inhibition Promiscuity of Dual Specific Thrombin and Factor Xa Blood Coagulation Inhibitors
Published in Structure (London) (10-01-2001)“…Background: A major current focus of pharmaceutical research is the development of selective inhibitors of the blood coagulation enzymes thrombin or factor Xa…”
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6
Effects of Telmisartan on Renal Excretory Function in Conscious Dogs
Published in Journal of international medical research (01-04-2001)“…The present study investigated the effects of telmisartan, a selective AT1 receptor antagonist, on renal function in dogs. Conscious female dogs were treated…”
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7
A highly selective telomerase inhibitor limiting human cancer cell proliferation
Published in The EMBO journal (17-12-2001)“…Telomerase, the ribonucleoprotein enzyme maintaining the telomeres of eukaryotic chromosomes, is active in most human cancers and in germline cells but, with…”
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8
Mechanism of Human Telomerase Inhibition by BIBR1532, a Synthetic, Non-nucleosidic Drug Candidate
Published in The Journal of biological chemistry (03-05-2002)“…Telomerase, a ribonucleoprotein acting as a reverse transcriptase, has been identified as a target for cancer drug discovery. The synthetic, non-nucleosidic…”
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9
Structure-Based Design of Novel Potent Nonpeptide Thrombin Inhibitors
Published in Journal of medicinal chemistry (25-04-2002)“…The clinical syndromes of thromboembolism are evoked by an excessive stimulation of the coagulation cascade. In this context, the serine protease thrombin…”
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10
Angiotensin II receptor antagonists
Published in Arzneimittel-Forschung (01-02-1993)“…The development of novel non-peptide compounds with high affinity for-angiotensin II (Ang II) receptors has greatly facilitated the subclassification of Ang II…”
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11
Heterocyclic thrombin inhibitors. Part 2: quinoxalinone derivatives as novel, potent antithrombotic agents
Published in Bioorganic & medicinal chemistry letters (21-07-2003)“…Quinoxalinone derivatives as prototypes of dual thrombin and factor Xa inhibitors have been discovered. Nanomolar inhibition of both coagulation enzymes…”
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12
Characterization of the nonpeptide angiotensin AT 1 receptor antagonist BIBR 363
Published in Pharmacological research (1995)Get full text
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13
Characterization of the nonpeptide angiotensin AT1 receptor antagonist BIBR 363
Published in Pharmacological research (01-01-1995)Get full text
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14
New cardiotonic agents--a promising approach for treatment of heart failure
Published in Trends in pharmacological sciences (Regular ed.) (01-05-1988)Get more information
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15
Heterocyclic thrombin inhibitors. Part 1: design and synthesis of amidino-phenoxy quinoline derivatives
Published in Bioorganic & medicinal chemistry letters (21-07-2003)“…Amidino-phenoxy quinoline derivatives represent a new class of potent thrombin inhibitors with good selectivity and remarkably low molecular weight ( M W:…”
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