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Nonpeptide glycoprotein IIB/IIIA inhibitors. 19. A new design paradigm employing linearly minimized, centrally constrained, exosite inhibitors
- Source :
- Bioorganic & Medicinal Chemistry Letters. 9:863-868
- Publication Year :
- 1999
- Publisher :
- Elsevier BV, 1999.
-
Abstract
- A new series of potent, linearly-minimized, orally active, selective GPIIb/IIIa inhibitors is identified. Thus 15 (L-750,034) achieves interaction via a constrained, non-turned conformation that maintains the proper distance between its charged termini and full sulfonamide exosite interaction. The diminutive stature and the proposed linear conformation of L-750,034 define a new paradigm for the conceptualization of RGD mimics.
- Subjects :
- Models, Molecular
Time Factors
Molecular model
medicine.drug_class
Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
Carboxamide
Platelet Glycoprotein GPIIb-IIIa Complex
Biochemistry
Inhibitory Concentration 50
Drug Discovery
medicine
Molecular Biology
Design paradigm
chemistry.chemical_classification
Organic Chemistry
Sulfonamide
Orally active
Models, Chemical
chemistry
Drug Design
Glycoprotein IIb/IIIa inhibitors
Benzamides
Benzene derivatives
Molecular Medicine
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 9
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....54676d5e171eef3ee1355b6e9ae419fa
- Full Text :
- https://doi.org/10.1016/s0960-894x(99)00104-3