Abstract
The further optimisation of the novel lead compound CGH752 (Fig. 1) is described. By introducing various substituents into the 6-position of the 3,3-dimethyltetrahydroquinoline (DMTHQS) ring we have been able to favourably affect the in vitro and in vivo activity, and the pharmacokinetics of such compounds. One of the inhibitors synthesised (CGH1484) is bioavailable and shows efficacy in animal models of thrombosis.
MeSH terms
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Administration, Oral
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Alanine / analogs & derivatives*
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Alanine / chemical synthesis
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Alanine / chemistry
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Alanine / pharmacokinetics
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Animals
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Antithrombins / chemical synthesis*
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Antithrombins / chemistry
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Antithrombins / pharmacokinetics*
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Biological Availability
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Chymotrypsin / antagonists & inhibitors
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Drug Design
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Fibrinolysin / antagonists & inhibitors
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Kinetics
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Molecular Conformation
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Molecular Structure
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Partial Thromboplastin Time
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Structure-Activity Relationship
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Sulfonamides / chemistry*
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Sulfonamides / pharmacokinetics
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Thiazoles / chemistry*
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Thiazoles / pharmacokinetics
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Thrombosis / drug therapy
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Trypsin / metabolism
Substances
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Antithrombins
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CGH 752
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Sulfonamides
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Thiazoles
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Chymotrypsin
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Trypsin
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Fibrinolysin
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Alanine