Search Results - "Lormeau, J C"
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Synthesis of thrombin-inhibiting heparin mimetics without side effects
Published in Nature (London) (01-04-1999)“…Unwanted side effects of pharmacologically active compounds can usually be eliminated by structural modifications. But the complex heterogeneous structure of…”
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2
Contribution of erythrocytes to thrombin generation in whole blood
Published in Thrombosis and haemostasis (01-03-1999)“…Thrombin generation (TG) initiated by diluted tissue-factor was investigated in whole human blood, in platelet-rich plasma (PRP), in platelet-poor plasma…”
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The effect of the synthetic pentasaccharide SR 90107/ORG 31540 on thrombin generation ex vivo is uniquely due to ATIII-mediated neutralization of factor Xa
Published in Thrombosis and haemostasis (01-12-1995)“…The inhibition of thrombin generation (TG) was studied in plasma from human volunteers after single subcutaneous administrations of 4000, 8000 or 12,000…”
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4
DX 9065A a novel, synthetic, selective and orally active inhibitor of factor Xa: in vitro and in vivo studies
Published in The Journal of pharmacology and experimental therapeutics (01-03-1996)“…DX 9065A is the first member of a newly developed series of synthetic and selective inhibitors of factor Xa. DX 9065A inhibited in a dose-dependent manner…”
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5
Comparative effects of two direct and indirect factor Xa inhibitors on free and clot-bound prothrombinase
Published in The Journal of pharmacology and experimental therapeutics (01-10-1997)“…Factor Xa, as with thrombin, binds to the clot and contributes to the propensity of thrombi to activate the coagulation system. The aim of this work was to…”
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6
Absence of cross-reactivity of SR90107A/ORG31540 pentasaccharide with antibodies to heparin-PF4 complexes developed in heparin-induced thrombocytopenia
Published in Blood coagulation & fibrinolysis (01-03-1997)“…New carbohydrate-based anticoagulants devoid of the side effects of unfractionated heparin are currently under development and show a major potential for…”
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7
Biochemical and Pharmacological Properties of SANORG 32701: Comparison With the `Synthetic Pentasaccharide' (SR 90107/ORG 31540) and Standard Heparin
Published in Circulation research (01-09-1996)“…SANORG 32701 is a new sulfated pentasaccharide obtained by total chemical synthesis. It is an analogue of the ``synthetic pentasaccharide'' (SR 90107/ORG…”
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Molecular profiling and weight determination of heparins and depolymerized heparins
Published in Journal of pharmaceutical sciences (01-06-1995)“…The recently proposed calibrant LHN-1 (lot F537; henceforth designated F537), for the molecular weight (MW) determination by high-performance size-exclusion…”
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9
Heparin reverses the procoagulant properties of stimulated endothelial cells
Published in Thrombosis and haemostasis (01-01-1996)“…We examined the ability of unfractionated heparin to modulate the procoagulant activities of stimulated endothelial cells (EC). Confluent human venous…”
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10
Chemical synthesis of glycosaminoglycans : new approaches to antithrombotic drugs
Published in Nature (London) (18-04-1991)“…Sanofi, Elf Aquitaine's pharmaceutical subsidiary, is a world leader in the manufacturing of antithrombotic drugs. The development of Heparin-based…”
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Synthesis and Pharmacological Properties of a Close Analogue of an Antithrombotic Pentasaccharide (SR 90107A/ORG 31540)
Published in Journal of medicinal chemistry (23-05-1997)“…The synthetic pentasaccharide (1) corresponding to the heparin sequence which binds to, and activates, antithrombin III (AT III) is a potent antithrombotic…”
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12
Structural determinants of heparin's growth inhibitory activity. Interdependence of oligosaccharide size and charge
Published in The Journal of biological chemistry (25-01-1989)“…The glycosaminoglycan heparin inhibits the growth of several cell types in vitro including smooth muscle cells and rat cervical epithelial cells. The…”
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13
New synthetic heparin mimetics able to inhibit thrombin and factor Xa
Published in Bioorganic & medicinal chemistry letters (19-04-1999)“…Synthetic pentadeca-, heptadeca- and nonadecasaccharides, comprising an antithrombin III (AT III) binding pentasaccharide prolonged at the non-reducing end by…”
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Comparative inhibition of extrinsic and intrinsic thrombin generation by standard heparin, a low molecular weight heparin and the synthetic ATIII-binding pentasaccharide
Published in Thrombosis and haemostasis (01-02-1993)“…The inhibiting effect of standard heparin, CY216 and the ATIII-binding synthetic pentasaccharide on extrinsic and intrinsic thrombin generation were quantified…”
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15
Antiproliferative effects of novel, nonanticoagulant heparin derivatives on vascular smooth muscle cells in vitro and in vivo
Published in The American journal of pathology (01-12-1991)“…The proliferation of vascular smooth muscle cells (VSMC) is strongly inhibited by whole heparin both in vitro and in vivo. To identify and characterize…”
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16
Preparation and anti-HIV activity of O-acylated heparin and dermatan sulfate derivatives with low anticoagulant effect
Published in Journal of medicinal chemistry (01-11-1993)“…In order to increase the ratio of anti-HIV activity to anticoagulant activity, glycosaminoglycan derivatives selectively substituted at OH and/or COOH groups…”
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17
Structural Determinants of the Capacity of Heparin to Inhibit the Proliferation of Vascular Smooth Muscle Cells. II. Evidence for a Pentasaccharide Sequence That Contains a 3-O-Sulfate Group
Published in The Journal of cell biology (01-05-1986)“…Earlier work from our laboratory demonstrated that heparin inhibited the proliferation of vascular smooth muscle cells in vivo and in vitro. Both anticoagulant…”
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The mode of action of CY216 and CY222 in plasma
Published in Thrombosis and haemostasis (23-01-1992)“…Three fractions of the low molecular weight heparin CY216 (fraxiparin, mean molecular weight [MMW] 5,090), with MMWs of respectively, 3,090, 4,400 and 7,910…”
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Contribution of monosaccharide residues in heparin binding to antithrombin III
Published in Biochemistry (Easton) (01-11-1985)“…The importance of 3-O- and 6-O-sulfated glucosamine residues within the heparin octasaccharide iduronic acid(1)---N-acetylglucosamine…”
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20
Heparin and low molecular weight heparins inhibit prothrombinase formation but not its activity in plasma
Published in Thrombosis and haemostasis (01-12-1994)“…Factor V activation is a critical step preceding prothrombinase formation. This study determined the contributions of factor Xa and thrombin, which activate…”
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