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C6 modification of the pyridinone core of thrombin inhibitor L-374,087 as a means of enhancing its oral absorption
- Source :
- Bioorganicmedicinal chemistry letters. 8(13)
- Publication Year :
- 1999
-
Abstract
- 1 (L-374,087) is a potent, selective, efficacious, and orally bioavailable thrombin inhibitor that contains a core 3-amino-2-pyridinone moiety. Replacement of the C6 pyridinone methyl group of 1 by a propyl group gave 5 (L-375,052), which retained all the excellent properties of 1, and also yielded higher plasma levels after oral dosing in dogs and rats.
- Subjects :
- Stereochemistry
medicine.drug_class
Pyridines
Pyridones
Clinical Biochemistry
Pharmaceutical Science
Administration, Oral
Biological Availability
Carboxamide
Pharmacology
Biochemistry
Chemical synthesis
Antithrombins
chemistry.chemical_compound
Thrombin
Dogs
Pharmacokinetics
Oral administration
Drug Discovery
Sulfanilamides
medicine
Moiety
Animals
Molecular Biology
Sulfonamides
biology
Chemistry
Organic Chemistry
Rats
Enzyme inhibitor
biology.protein
Molecular Medicine
Methyl group
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 8
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....ce0cae6c611da785a9c22fd3e180c35c