Cholinergic drugs and cholinesterase inhibitors

Immunotag™ Human CHRM2 (Cholinergic Receptor, Muscarinic 2) ELISA

Immunotag™ Mouse CHRM2 (Cholinergic Receptor, Muscarinic 2) ELISA

Immunotag™ Rat CHRM2 (Cholinergic Receptor, Muscarinic 2) ELISA

General description The protein encoded by this gene contains a paired-like homeodomain most similar to that of the Drosophila aristaless gene product. The encoded protein plays a central role in development of the autonomic nervous system.

Application Neostigmine bromide has been used as an acetyl cholinesterase (AChE) inhibitor: to control reaction specificity of acetylcholinesterase in coronal organ of Botryllus schlosseri . to study its effects on abnormal contraction of

Application Neostigmine bromide has been used as an acetyl cholinesterase (AChE) inhibitor: to control reaction specificity of acetylcholinesterase in coronal organ of Botryllus schlosseri . to study its effects on abnormal contraction of

Application Neostigmine bromide has been used as an acetyl cholinesterase (AChE) inhibitor: to control reaction specificity of acetylcholinesterase in coronal organ of Botryllus schlosseri . to study its effects on abnormal contraction of

Biochem/physiol Actions PF-04995274 favors the production of cyclic adenosine monophosphate (cAMP). PF-04995274 is a potent partial agonist of serotonin 5HT4 receptor with Ki = 0.

Biochem/physiol Actions PF-04995274 favors the production of cyclic adenosine monophosphate (cAMP). PF-04995274 is a potent partial agonist of serotonin 5HT4 receptor with Ki = 0.

Biochem/physiol Actions (-)-Phenserine, a phenylcarbamate derivative, is a selective, non-competitive inhibitor of acetylcholinesterase (AChE). (-)-Phenserine produces rapid, potent, and long-lasting AChE inhibition, in vivo .

Biochem/physiol Actions (-)-Phenserine, a phenylcarbamate derivative, is a selective, non-competitive inhibitor of acetylcholinesterase (AChE). (-)-Phenserine produces rapid, potent, and long-lasting AChE inhibition, in vivo .

PQCA is a highly selective and potent muscarinic M1 receptor positive allosteric modulator. PQCA has an EC 50 value of 49 nM and 135 nM on rhesus and human M1 receptor , respectively. PQCA is inactive for other muscarinic receptors. PQCA has