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N1-sterically hindered 2H-imidazol-2-one angiotensin II receptor antagonists: The conversion of surmountable antagonists to insurmountable antagonists
- Source :
- Bioorganic & Medicinal Chemistry Letters. 3:1055-1060
- Publication Year :
- 1993
- Publisher :
- Elsevier BV, 1993.
-
Abstract
- The surmountable (competitive) N 1 -(2-methylphenyl)-2H-imidazol-2-one angiotensin II receptor antagonist SC-54628 is converted to an insurmountable (noncompetitive) antagonist SC-54629 by the addition of a methyl group at the 6-position of the phenyl ring.
- Subjects :
- Steric effects
Angiotensin receptor
Stereochemistry
Organic Chemistry
Clinical Biochemistry
Antagonist
Pharmaceutical Science
Angiotensin II receptor antagonist
Ring (chemistry)
Biochemistry
HYDIA
chemistry.chemical_compound
chemistry
Competitive antagonist
Drug Discovery
Molecular Medicine
Molecular Biology
Methyl group
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi...........45e31096603038f887f225236b63745d
- Full Text :
- https://doi.org/10.1016/s0960-894x(00)80286-3