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Delequamine

CAT: 0804-HY-106874-01Size: 1 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-106874-01Size:1 mg
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Description
Delequamine (RS-15385-197) is an orally active and selective α2-adrenergic receptor antagonist with a pKi of 9.5 for α2-adrenoceptors in rat cortex. Delequamine shows >1000 fold selectivity against 5-HT1A receptors and α1-adrenoceptors. Delequamine can be used for the study of erectile dysfunction[1].
CAS Number
119905-05-4
Product Name Alternative
RS-15385-197
UNSPSC
12352005
Target
Adrenergic Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Neuroscience-Neuromodulation
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/delequamine.html
Solubility
10 mM in DMSO
Smiles
CS(=O)(N1[C@@]2([H])C[C@@]3([H])C4=CC=C(OC)C=C4CCN3C[C@@]2([H])CCC1)=O
Molecular Formula
C18H26N2O3S
Molecular Weight
350.48
References & Citations
[1]Tallentire D, et al. Modulation of sexual behaviour in the rat by a potent and selective alpha 2-adrenoceptor antagonist, delequamine (RS-15385-197) . Br J Pharmacol. 1996;118 (1) :63-72.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
No Development Reported
Isoform
5-HT1 Receptor; α adrenergic receptor