GW 328267
GW 328267 is an A2A receptor agonist. GW 328267 can be used for research of asthma, COPD and upper respiratory inflammatory disease.
For research use only. We do not sell to patients.
- CAS No.: 210237-78-8
- Formula: C21H26N10O4
- Molecular Weight:482.50
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Adenosine Receptor Isoforms
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Biological Activity
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A2a adenosine receptor |
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| CHO | EC50 |
8.8 nM
Compound: 1
|
Potency against cAMP formation in CHO cells expressing recombinant human A2A receptor
Potency against cAMP formation in CHO cells expressing recombinant human A2A receptor
|
[PMID: 15267242] |
| CHO | EC50 |
1 μM
Compound: 1
|
Potency against cAMP formation in CHO cells expressing recombinant human A2B receptor
Potency against cAMP formation in CHO cells expressing recombinant human A2B receptor
|
[PMID: 15267242] |
| CHO | EC50 |
4.2 nM
Compound: GW-328267
|
Agonist activity at human adenosine A3 receptor expressed in CHO cells by GTPPgammaS binding assay
Agonist activity at human adenosine A3 receptor expressed in CHO cells by GTPPgammaS binding assay
|
[PMID: 20031406] |
| CHO | EC50 |
51 nM
Compound: GW-328267
|
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as effect on cAMP production by luciferase reporter gene assay
Agonist activity at human adenosine A2B receptor expressed in CHO cells assessed as effect on cAMP production by luciferase reporter gene assay
|
[PMID: 20031406] |
| CHO | EC50 |
882 nM
Compound: GW-328267
|
Agonist activity at human adenosine A1 receptor expressed in CHO cells by GTPPgammaS binding assay
Agonist activity at human adenosine A1 receptor expressed in CHO cells by GTPPgammaS binding assay
|
[PMID: 20031406] |
| CHO | IC50 |
5 nM
Compound: 76
|
Antagonist activity at human adenosine A3 receptor expressed in CHO cells assessed as blockade of Cl-IB-MECA-mediated inhibition of forskolin-stimulated [3H]cAMP accumulation by scintillation counter
Antagonist activity at human adenosine A3 receptor expressed in CHO cells assessed as blockade of Cl-IB-MECA-mediated inhibition of forskolin-stimulated [3H]cAMP accumulation by scintillation counter
|
[PMID: 22468757] |
| PBMC | IC50 |
1.3 nM
Compound: GW-328267
|
Antiinflammatory activity in human PBMC assessed as inhibition of LPS-induced TNFalpha production after 20 hrs by ELISA
Antiinflammatory activity in human PBMC assessed as inhibition of LPS-induced TNFalpha production after 20 hrs by ELISA
|
[PMID: 20031406] |
| PBMC | IC50 |
2.9 nM
Compound: GW-328267
|
Antiinflammatory activity in rat PBMC assessed as inhibition of LPS-induced TNFalpha production after 20 hrs by ELISA
Antiinflammatory activity in rat PBMC assessed as inhibition of LPS-induced TNFalpha production after 20 hrs by ELISA
|
[PMID: 20031406] |
Chemical Information
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CAS No. 210237-78-8
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Molecular Weight 482.50
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Formula C21H26N10O4
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SMILES
O[C@H]1[C@@H](O[C@H](C2=NN(N=N2)CC)[C@H]1O)N3C4=NC(N[C@H](CO)CC5=CC=CC=C5)=NC(N)=C4N=C3
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)