A-61603

A-61603 is a selective α1A-adrenergic receptor agonist[1]. A-61603 increases the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro[2].

Product Specifications

CAS Number

[107756-30-9]

UNSPSC

12352005

Target

Adrenergic Receptor

Type

Reference compound

Related Pathways

GPCR/G Protein; Neuronal Signaling

Applications

Neuroscience-Neuromodulation

Field of Research

Cardiovascular Disease

Assay Protocol

https://www.medchemexpress.com/a-61603.html

Purity

99.16

Solubility

DMSO : 20 mg/mL (ultrasonic; warming)

Smiles

CS(=O)(NC1=C2CCCC(C3=NCCN3)C2=CC=C1O)=O.Br

Molecular Formula

C14H20BrN3O3S

Molecular Weight

390.30

References & Citations

[1]Meyer MD, et al. Synthesis and in vitro characterization of N-[5- (4,5-dihydro-1H-imidazol-2-yl) -2-hydroxy-5,6,7,8- tetrahydronaphthalen-1-yl]methanesulfonamide and its enantiomers: A novel selective α1A receptor agonist. J. Med. Chem. 39 (20), 4116-4119 (1996) .