(-) -Penbutolol
(-) -Penbutolol ((S) -Penbutolol) is a potent β-adrenoceptor and 5-HT receptor antagonist with Ki values of 11.6 nM and 11.9 nM for 5-HT in rat cornu ammonis 1 (CA1) and human CA3[1][2].
Product Specifications
CAS Number
[38363-40-5]
Product Name Alternative
(S) -Penbutolol; (-) -Isopenbutolol
UNSPSC
12352005
Hazard Statement
H315-H319-H320
Target
5-HT Receptor; Adrenergic Receptor
Type
Reference compound
Related Pathways
GPCR/G Protein; Neuronal Signaling
Applications
Metabolism-protein/nucleotide metabolism
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/minus-penbutolol.html
Solubility
10 mM in DMSO
Smiles
O[C@H](COC1=CC=CC=C1C2CCCC2)CNC(C)(C)C
Molecular Formula
C18H29NO2
Molecular Weight
291.43
Precautions
P264-P280-P302+P352-P305+P351+P338-P362
References & Citations
[1]Hjorth S, et al. In vivo microdialysis evidence for central serotonin1A and serotonin1B autoreceptor blocking properties of the beta adrenoceptor antagonist (-) penbutolol. J Pharmacol Exp Ther. 1993 May;265 (2) :707-12.|[2]M E Castro, et al. Affinity of (±) -Pindolol, (-) -Penbutolol, and (-) -Tertatolol for Pre- and Postsynaptic Serotonin 5-HT1A Receptors in Human and Rat Brain. Journal of Neurochemistry, Volume 75, Issue 2, p. 755-762.|[3]Gartside SE, et al., Effects of (-) -tertatolol, (-) -penbutolol and (+/-) -pindolol in combination with paroxetine on presynaptic 5-HT function: an in vivo microdialysis and electrophysiological study. Br J Pharmacol. 1999 May;127 (1) :145-52.
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
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