Galantamine hydrobromide

Galanthamine hydrobromide is a derivative of galanthamine, which is an anticholinestrase alkaloid derived from genus Lycoris (Amaryllidaceae) or snowdrop. This compound is used for the treatment of Alzheimer′s disease (AD).

General description This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate.

Galanthamine-O-methyl-d3 is a deuterated selective acetylcholinesterase inhibitor.Galanthamine-O-methyl-d3is a labeled inhibitor of acetylcholinesterase.

Galantide TFA is a reversible and non-specific galanin (GAL) receptor antagonist. Galantide TFA dose-dependently shows antagonism to galanin-induced K + conductance with an IC 50 value of 4 nM. Galantide TFA can be used for the research of

Galantide TFA is a reversible and non-specific galanin (GAL) receptor antagonist. Galantide TFA dose-dependently shows antagonism to galanin-induced K + conductance with an IC 50 value of 4 nM. Galantide TFA can be used for the research of

Galantide TFA is a reversible and non-specific galanin (GAL) receptor antagonist. Galantide TFA dose-dependently shows antagonism to galanin-induced K + conductance with an IC 50 value of 4 nM. Galantide TFA can be used for the research of

Biochem/physiol Actions Selective blocker of the TTX-sensitive Na + channels, without influence on the activation threshold of Na + channels. Warning Protect from light.

M40 is a potent, non-selective galanin receptor antagonist.In VitroM40 (1 μM) displaces [mono[ 125 IJodo-Tyr 26 ]galanin from binding sites in the hippocampus, hypothalamus, and spinal cord. M40 has a lower affinity than galanin for all membranes.

M40 is a potent, non-selective galanin receptor antagonist.In VitroM40 (1 μM) displaces [mono[ 125 IJodo-Tyr 26 ]galanin from binding sites in the hippocampus, hypothalamus, and spinal cord. M40 has a lower affinity than galanin for all membranes.

M40 is a potent, non-selective galanin receptor antagonist.In VitroM40 (1 μM) displaces [mono[ 125 IJodo-Tyr 26 ]galanin from binding sites in the hippocampus, hypothalamus, and spinal cord. M40 has a lower affinity than galanin for all membranes.

M40 is a potent, non-selective galanin receptor antagonist.In VitroM40 (1 μM) displaces [mono[ 125 IJodo-Tyr 26 ]galanin from binding sites in the hippocampus, hypothalamus, and spinal cord. M40 has a lower affinity than galanin for all membranes.

Biochem/physiol Actions M871 is a type 2-selective galanin receptor antagonist (GalR2/GalR1 K i = 13.1/410 nM by competitive binding against 0.