1. GPCR/G Protein Neuronal Signaling
  2. Adrenergic Receptor
  3. (±)-Befunolol

(±)-Befunolol is a β-adrenoceptor blocking agent.

For research use only. We do not sell to patients.

(±)-Befunolol Chemical Structure

(±)-Befunolol Chemical Structure

CAS No. : 39552-01-7

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Description

(±)-Befunolol is a β-adrenoceptor blocking agent.

IC50 & Target

Adrenoreceptor[1]

In Vitro

A β-adrenoceptor blocking agent, Befunolol, is found to has intrinsic sympathomimetic activities in isolated right atria, trachea and taenia caecum of guinea pig (intrinsic activities are 0.22-0.28). The pD2-values of Befunolol estimated in the isolated organs are significantly different from its pA2-values against isoprenaline. Befunolol interacts with the beta-adrenoceptor where there may be two different sites: one site for agonistic action and the other for competitive antagonistic action. The intrinsic activity of Befunolol may be equal to its selectivity for both the sites[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

291.34

Formula

C16H21NO4

CAS No.
SMILES

CC(C1=CC2=CC=CC(OCC(O)CNC(C)C)=C2O1)=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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(±)-Befunolol Related Classifications

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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(±)-Befunolol
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HY-101752
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