Fig. 1 · Structure

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Tamsulosin

Cat. No. A12657 CAS 106133-20-4

alpha-1A/alpha-1B-adrenoceptor antagonist

Tamsulosin is an alpha1a-selective alpha blocker used in the symptomatic treatment of benign prostatic hyperplasia (BPH).

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Biological Activity

Target & Activity

Target Activity Value
α adrenergic receptor  
α1-adrenergic receptor  

Cellular Effect

Cell Line Activity Value Description Reference
CHO-K1 EC50 0.13 nM Intrinsic activity at human alpha1B adrenergic receptor expressed in CHOK1 cells co-expressing aequorin assessed as inhibition of agonist induced calcium mobilization preincubated for 15 mins followed by agonist addition measured for 20 secs in presence o [PMID: 27658792]
HEK293 IC50 1.4 nM Antagonist activity at human full-length N-terminal SNAP-tagged alpha1D adrenoceptor expressed in HEK293 cells assessed as inhibition of agonist-induced calcium mobilization preincubated for 10 mins followed by agonist addition by fluo-4 AM dye-based assa [PMID: 27709945]
HEK293 IC50 2.2 nM Antagonist activity at human full-length N-terminal SNAP-tagged alpha1A adrenoceptor expressed in HEK293 cells assessed as inhibition of agonist-induced calcium mobilization preincubated for 10 mins followed by agonist addition by fluo-4 AM dye-based assa [PMID: 27709945]
HEK293 IC50 4.8 nM Antagonist activity at human full-length N-terminal SNAP-tagged alpha1B adrenoceptor expressed in HEK293 cells assessed as inhibition of agonist-induced calcium mobilization preincubated for 10 mins followed by agonist addition by fluo-4 AM dye-based assa [PMID: 27709945]

Specifications

Manufacturer Adooq Bioscience
Actions Antagonist
CAS Number 106133-20-4
Applications alpha-1A/alpha-1B-adrenoceptor antagonist
Formula C20H28N2O5S
Molecular Weight 408.51
SMILES
CCOC1=CC=CC=C1OCCN[C@H](C)CC2=CC(=C(C=C2)OC)S(=O)(=O)N

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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