Biological Information

Background Information:

Adrenoreceptors belong to the superfamily of G protein-coupled seven transmembrane proteins. G-protein-coupled receptors constitute one of the major signal transduction systems in eukaryotic cells. Coding sequences for these receptors, in those regions believed to contribute to the agonist-antagonist binding site, are strongly conserved across mammalian species. Adrenoreceptors are found in most peripheral tissue and within the central nervous system.

Family:

GPCR

Sub Family:

Adrenoceptor

Class:

Class A

Protein Name:

alpha1D

Uniprot Number:

P25100

Protein Aliases:

Alpha-1D adrenoreceptor|Alpha-1D adrenoceptor|Alpha-adrenergic receptor 1a

Gene Name:

ADRA1D

Gene ID:

146

Gene Aliases:

ADRA1R|ADRA1A|ADRA1

Accession Number:

NM_000678

Organism:

Human

Construct Details:

Full Length, Recombinant

Assay Information

Assay Type:

Biochemical

Assay Sub Type:

Binding

Detection Method:

Radiometry

Measured Response:

Scintillation

Testing Information

Procedure Summary:

This assay measures binding of [³H]Prazosin to adrenergic a1D receptors. Membranes (obtained from HEK-293 cells) encoding the human adrenergic a1D receptor are used in modified Tris-HCl, pH 7.4 buffer using standard techniques. A 50 μg‡ aliquot of membrane is incubated with 0.6 nM [³H]Prazosin for 60 minutes at 25°C. Non-specific binding is estimated in the presence of 10 μM phentolamine. Membranes are filtered and washed 3 times and the filters are counted to determine [³H]Prazosin specifically bound. Compounds are screened at 10 μM.
Note: ‡Membrane protein may change from lot to lot, the concentration used will be adjusted if necessary.

Ligand:

[³H] Prazosin

Ligand Kd (nM):

0.58

Ligand Concentration:

0.6 nM

Non Specific:

10 µM Phentolamine

Incubation:

60 min at 25°C

Control Inhibitor:

Prazosin

Criteria For Significance:

≥ 50% of max stimulation or inhibition

Test Concentration / Dose:

Suggested concentration for initial testing is 10 uM

Test Sample Requirements:

Minimum for 1) Screen: 25 μl of 10 mM stock -OR- 1 mg (pre-weighed). 2) Dose Response: 60 μl of 10 mM stock -OR- 1 mg (pre-weighed).

Minimum Order Quantity:

2

Turnaround Time

Standard:

15 Business Days

Reference Compound Data

PubChem ID

2325

Name

Benoxathian

Measurement

0.0076μM - IC50

PubChem ID

3822

Name

Ketanserin

Measurement

0.027μM - IC50

PubChem ID

4893

Name

Prazosin

Measurement

0.00088μM - IC50

PubChem ID

5265

Name

Spiperone

Measurement

0.0095μM - IC50

PubChem ID

5685

Name

WB-4101

Measurement

0.0027μM - IC50

PubChem ID

5709

Name

Xylometazoline

Measurement

2μM - IC50

PubChem ID

5775

Name

Phentolamine

Measurement

0.054μM - IC50

PubChem ID

8969

Name

Yohimbine

Measurement

0.91μM - IC50

PubChem ID

104973

Name

Chloroethylclonidine

Measurement

2.6μM - IC50

PubChem ID

643606

Name

Rauwolscine

Measurement

1.5μM - IC50

Clinical Relevance

Therapeutic Area:

Cardiovascular

Adverse / Beneficial Action:

Adrenergic a1D receptor antagonism may be useful in the treatment of hypertension with minimal associated orthostatic hypotension.

Additional Information

Brand:

LeadHunter

Testing Location:

Taiwan - Taipei

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