18397-07-4

18397-07-4 structure

Name: pereirine
Chemical Name: geissoschizoline
CAS Number: 18397-07-4
Molecular Formula: C₁₉H₂₆N₂O
Molecular Weight: 298.42300
Catalog: Signaling Pathways Neuronal Signaling AChE
Create Date: 2016-06-07 08:13:41
Modify Date: 2025-08-20 13:01:20
Geissoschizoline ((+)-Geissoschizoline) is a potent inhibitor of human AChE/BChE, with IC50s of 20.40 µM and 10.21 µM, respectively. Geissoschizoline emerges as a possible multi-target prototype that can be very useful in studies of preventing neurodegeneration and restoring neurotransmission. Geissoschizoline aiso is a potent anti-inflammatory agent[1].

Name	geissoschizoline

Description	Geissoschizoline ((+)-Geissoschizoline) is a potent inhibitor of human AChE/BChE, with IC50s of 20.40 µM and 10.21 µM, respectively. Geissoschizoline emerges as a possible multi-target prototype that can be very useful in studies of preventing neurodegeneration and restoring neurotransmission. Geissoschizoline aiso is a potent anti-inflammatory agent[1].
Related Catalog	Research Areas >> Inflammation/Immunology Research Areas >> Neurological Disease Signaling Pathways >> Neuronal Signaling >> AChE
Target	IC50: 20.40 µM (AChE), 10.21 µM (BChE)[1]
In Vitro	Geissoschizoline(1 μM; 48 hours) significantly reduces production of TNF-α and NO in LPS-stimulated microglial cells [1]. Geissoschizoline(1, 10 and 30 μM; 24 hours) shows no cytotoxicity to LPS-stimulated microglial cells[1] Cell Viability Assay[1] Cell Line: LPS-stimulated microglial cells (pre-incubated with various concentrations (0.1- 10 μM) of geissoschizoline for 1 hour) Concentration: 1 μM Incubation Time: 48 hours Result: Reduced neuroinflammation and increased neuroprotection, also restored synaptic transmission. Cell Cytotoxicity Assay[1] Cell Line: LPS-stimulated microglial cells Concentration: 1, 10 and 30 μM Incubation Time: 24 hours Result: Did not affect cell viability.
References	[1]. Josélia A Lima, et al. Geissoschizoline, a promising alkaloid for Alzheimer's disease: Inhibition of human cholinesterases, anti-inflammatory effects and molecular docking. Bioorg Chem. 2020 Nov;104:104215.