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New pyrimido[5,4-b]indoles and [1]benzothieno[3,2-d]pyrimidines: High affinity ligands for the α1-adrenoceptor subtypes
- Source :
- Bioorganic & Medicinal Chemistry Letters. 16:6200-6203
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- A number of new pyrimido[5,4-b]indole and [1]benzothieno[3,2-d]pyrimidine derivatives were synthesized and evaluated for their binding and functional properties at alpha(1)-adrenergic receptor (alpha(1)-AR) subtypes. They behaved as potent alpha(1)-AR antagonists. In binding experiments, some of them (RC24 and RC23) showed very high affinity for the alpha(1D)-AR subtype.
- Subjects :
- Male
Indoles
synthesis
Pyrimidine
Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
Alpha (ethology)
Ligands
ligand
Biochemistry
Chemical synthesis
Structure-Activity Relationship
chemistry.chemical_compound
Receptors, Adrenergic, alpha-1
alpha1D-adrenoceptor subtype
Drug Discovery
Animals
Structure–activity relationship
Receptor
Molecular Biology
Indole test
Ligand
Organic Chemistry
Prostate
antagonist
Rats
alpha1-adrenoceptor
Pyrimidines
chemistry
Lactam
Molecular Medicine
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....012f8e31865088c822ec2f6dda73d282