Back to Search
Start Over
Selective, high affinity A2B adenosine receptor antagonists: N-1 monosubstituted 8-(pyrazol-4-yl)xanthines
- Source :
- Bioorganic & Medicinal Chemistry Letters. 18:1397-1401
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- A series of N-1 monosubstituted 8-pyrazolyl xanthines have been synthesized and evaluated for their affinity for the adenosine receptors (AdoRs). We have discovered two compounds 18 (CVT-7124) and 28 (CVT-6694) that display good affinity for the A(2B) AdoR (K(i)=6 nM and 7 nM, respectively) and greater selectivity for the human A(1), A(2A), and A(3) AdoRs (>1000-, >830-, and >1500-fold; >850-, >700-, and >1280-fold, respectively). CVT-6694 has been shown to block the release of interleukin-6 and monocyte chemotactic protein-1 from bronchial smooth muscle cells (BSMC), a process believed to be promoted by activation of A(2B) AdoR.
- Subjects :
- Stereochemistry
Clinical Biochemistry
Pharmaceutical Science
CHO Cells
Receptor, Adenosine A2B
Binding, Competitive
Biochemistry
Chemical synthesis
Substrate Specificity
Cricetulus
Cricetinae
Drug Discovery
medicine
Animals
Humans
Uracil
Receptor
Molecular Biology
Chemistry
Monocyte
Organic Chemistry
Antagonist
Adenosine
Adenosine receptor
In vitro
Adenosine A2 Receptor Antagonists
Kinetics
medicine.anatomical_structure
Xanthines
Pyrazoles
Molecular Medicine
Selectivity
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....f0ad952cae86b92e38484b3004599916
- Full Text :
- https://doi.org/10.1016/j.bmcl.2008.01.008