L4376

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L4376

Sigma

 

α-Lobeline hydrochloride

~95% (HPLC), powder

Synonym:(−)-Lobeline hydrochloride, 2-[6-(2-Hydroxy-2-phenylethyl)-1-methyl-2-piperidinyl]-1-phenylethanone hydrochloride
CAS Number:134-63-4
Linear Formula:C22H27NO2 · HCl
Molecular Weight:373.92
Beilstein Registry Number:3920196
EC Number:205-150-2
MDL number:MFCD00082455

Description

Biochem/physiol ActionsAgonist at high-affinity neuronal nicotinic acetylcholine receptors; respiratory stimulant. Inhibits synaptosomal accumulation of dopamine by interaction with the tetrabenazine binding site of the vesicular monoamine transporter (VMAT2). Blocks amphetamine-induced dopamine release.

Properties

assay~95% (HPLC)
formpowder
color white to off-white
solubilityH2O: 25 mg/mL
Gene Informationhuman ... SLC18A2(6571)

Safety

Personal Protective EquipmentEyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard CodesT
Risk Statements23/25
Safety Statements36/37/39-45
RIDADRUN 1544 6.1/PG 3
WGK Germany3
RTECSOJ8490100

References

referenceToth, P.T. and Vizi, E.S., Lobeline inhibits Ca2+ current in cultured neurones from rat sympathetic ganglia. Eur. J. Pharmacol. 363, 75-80, (1998)
 Damaj, M.I., et al., Pharmacology of lobeline, a nicotinic receptor ligand. J. Pharmacol. Exp. Ther. 282, 410-419, (1997)
 Vizi, E.S., and Lendvai, B., Modulatory role of presynaptic nicotinic receptors in synaptic and non-synaptic chemical communication in the central nervous system. Brain Res. Brain Res. Rev. 30, 219-235, (1999)
 Flammia, D., et al., Lobeline: structure-affinity investigation of nicotinic acetylcholinergic receptor binding. J. Med. Chem. 42, 3726-3731, (1999)
MerckMerck 13,5572
BeilsteinBeil. 21,V,12,627