A-61603

• Description:

  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].

• 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) .

• Shipping Conditions:

  Blue Ice

• Storage Conditions:

  -20°C (Powder, sealed storage, away from moisture)

• Scientific Category:

  Reference compound1

• Clinical Information:

  No Development Reported

• Isoform:

  α adrenergic receptor

• CAS Number:

  [107756-30-9]