β2-adrenoceptor agonist 1
β2-adrenoceptor agonist 1 is a β2-adrenoceptor agonist with an EC50 of 7 pM. β2-adrenoceptor agonist 1 induces cAMP accumulation and airway/tracheal smooth muscle relaxation. β2-adrenoceptor agonist 1 inhibits inflammatory cell activity, reduces inflammatory cytokine production, and decreases mast cell infiltration. β2-adrenoceptor agonist 1 can be used for asthma research.
For research use only. We do not sell to patients.
- Formula: C22H28N2O5
- Molecular Weight:400.47
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Adrenergic Receptor Isoforms
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Biological Activity
Description
IC50 & Target
[1]|
β2 adrenoceptor 7 pM (EC50) |
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| BEAS-2B | CC50 |
50.07 μM
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Cytotoxicity against human bronchial epithelial BEAS-2B cells assessed as viability reduction after 48 hrs incubation by CCK-8 assay.
Cytotoxicity against human bronchial epithelial BEAS-2B cells assessed as viability reduction after 48 hrs incubation by CCK-8 assay.
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j.ejmech.2026.119297 |
| HEK-293T | CC50 |
33.39 μM
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Cytotoxicity against human embryonic kidney HEK293T cells assessed as viability reduction after 48 hrs incubation by CCK-8 assay.
Cytotoxicity against human embryonic kidney HEK293T cells assessed as viability reduction after 48 hrs incubation by CCK-8 assay.
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j.ejmech.2026.119297 |
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Human bronchial epithelial BEAS-2B and human embryonic kidney HEK293T cells
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Concentration:10 μM; 20 μM
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Incubation Time:48 h (C3); 2 h (CCK-8)
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Result:At 10 μM, C3 was non-cytotoxic in BEAS-2B and showed no significant cytotoxicity in HEK293T cells.
At 20 μM, C3 remained non-toxic in BEAS-2B, whereas HEK293T cells showed dose-dependent cytotoxicity.
C3 CC50 = 50.07 μM in BEAS-2B and 33.39 μM in HEK293T.
Parmacokinetics
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:BALB/c (female, 6-8 weeks old)[1]
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Dosage:100 μg/kg/day (228.9 nmol/kg/day); 200 μg/kg/day (458.5 nmol/kg/day)
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Administration:inhalation; once daily; 15 days
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Result:At 100 μg/kg/day, compound C3 did not improve lung function in asthmatic mice.
At 200 μg/kg/day, compound C3 improved Peak Expiratory Flow (PEF), Maximal Mid-Expiratory Flow (MMEF), Dynamic Compliance (Cdyn), Forced Vital Capacity (FVC), and Forced Expiratory Volume in 0.1 s (FEV0.1) to levels comparable to the positive-control group.
Both 100 and 200 μg/kg/day compound C3 reduced total white blood cell count in bronchoalveolar lavage fluid (BALF).
Differential cell counting showed reductions in eosinophils, neutrophils, and lymphocytes in groups receiving compound C3 compared with the model group.
Compound C3 reduced IL-4, IL-5, and IL-13 levels in BALF, lung tissue, and serum, with the 200 μg/kg/day group showing efficacy comparable to the positive control.
Toluidine blue (HY-D0220) staining showed dose-dependent improvement in lung histopathology, and the 200 μg/kg/day group had a reduction in mast cell numbers comparable to the positive control.
H&E staining confirmed protective effects on lung histopathology; the 200 μg/kg/day group showed an effect comparable to the positive control.
Chemical Information
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Molecular Weight 400.47
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Formula C22H28N2O5
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SMILES
COC1=C(C=CC=C1)CCC(NCC(C2=CC=C(C3=C2OCC(N3)=O)O)O)(C)C
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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)