Chemical Name: (3aS)-cis-1,2,3,3a,8,8a-Hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indol-5-ol methylcarbamate hemisulfate
Biological ActivityCholinesterase inhibitor.
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Anticholinesterases: medical applications of neurochemical principles.
Millard and Broomfield
Citations for Physostigmine hemisulfate
The citations listed below are publications that use Tocris products. Selected citations for Physostigmine hemisulfate include:
6 Citations: Showing 1 - 6
Impact of Altered Cholinergic Tones on the Neurovascular Coupling Response to Whisker Stimulation.
Authors: Lecrux Et al.
J Neurosci 2017;37:1518
Cholinergic and ghrelinergic receptors and KCNQ channels in the medial PFC regulate the expression of palatability.
Authors: Parent Et al.
Proc Natl Acad Sci U S A 2015;9:284
Muscarinic regulation of DA and glutamate transmission in the nucleus accumbens.
Authors: Shin Et al.
Front Neurosci 2015;112:8124
Energy substrates that fuel fast neuronal network oscillations.
Authors: Galow Et al.
J Neurosci 2014;8:398
Oxygen consumption rates during three different neuronal activity states in the hippocampal CA3 network.
Authors: Huchzermeyer Et al.
J Cereb Blood Flow Metab 2013;33:263
Input-specific plasticity at excitatory synapses mediated by endocannabinoids in the dentate gyrus.
Authors: Chiu and Castillo
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