
CAS 1135242-13-5
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Found 8 products.
VU 0357017 Hydrochloride
CAS:Formula:C18H28ClN3O3Purity:98%Color and Shape:SolidMolecular weight:369.88624-[[2-[(2-Methylbenzoyl)Amino]Ethyl]Amino]-1-Piperidinecarboxylic Acid Ethyl Ester Monohydrochloride
CAS:4-[[2-[(2-Methylbenzoyl)Amino]Ethyl]Amino]-1-Piperidinecarboxylic Acid Ethyl Ester MonohydrochloridePurity:99%Molecular weight:369.9g/molVU0357017 hydrochloride
CAS:<p>VU0357017 hydrochloride (ML071 hydrochloride) is highly selective M1 agonists act at an allosteric site to activate the receptor (EC50: 477 ± 172 nM; Pec50: 6.</p>Formula:C18H28ClN3O3Purity:99% - 99.97%Color and Shape:SolidMolecular weight:369.89Ethyl 4-((2-(2-methylbenzamido)ethyl)amino)piperidine-1-carboxylate hydrochloride
CAS:Purity:≥98%(HPLC)Molecular weight:369.8900146VU 0357017 Hydrochloride
CAS:Controlled Product<p>Applications VU0357017 is a subtype-selective M1 muscarinic acetylcholine allosteric agonist. VU0357017 has a potency of 200 nM and Achmax of 81% and had no activity at M2-M5 up to the highest concentrations tested and also had little or no detectable antagonist activity at any other mAChR subtype at concentrations over 2 orders of magnitude higher than those required to activate M1 or activity at a large panel of GPCRs, ion channels, and transporters. In contrast, TBPB inhibited responses to ACh at each of the other mAChR subtypes. VU0357017 was active in reversing cognitive deficits induced by Scopolamine (S200000) in a preclinical rodent model.<br>References Bridges, et al.: Bioorg. Med. Chem. Lett., 20, 1972 (2010); Lebois, et al.: ACS Chem. Neurosci., 1, 104 (2010),<br></p>Formula:C18H27N3O3·ClHColor and Shape:NeatMolecular weight:369.886VU 0357017 hydrochloride
CAS:<p>Agonist of muscarinic receptors M1 and M4</p>Formula:C18H28ClN3O3Purity:Min. 95%Molecular weight:369.89 g/mol






