1423014-09-8

Basic information

• Product Name: ethyl 4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate
• Synonyms: ethyl 4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate
• CAS NO: 1423014-09-8
• Molecular Weight: 231.294
• Mol File: 1423014-09-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate(1423014-09-8)
• EPA Substance Registry System: ethyl 4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate(1423014-09-8)

Safety Data

• Hazardous Substances Data: 1423014-09-8(Hazardous Substances Data)

Upstream product

• 98977-34-5 1-tert-butyl 3-ethyl 4-oxopiperidine-1,3-dicarboxylate 
• 176525-98-7 1-(1,1-dimethylethyl) 3-ethyl 4-{[(trifluoromethyl)sulfonyl]oxy}-1,2,5,6-tetrahydropyridine-1,3-dicarboxylate 
• 170837-88-4 1-tert-butyl 3-ethyl 4-triflate-5,6-dihydropyridine-1,3(2H)-dicarboxylate 

Downstream Products

• 1423014-63-4 C₂₃H₂₇NO₃ 
• 1423014-84-9 ethyl 1-n-butyl-4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate 
• 1423014-83-8 ethyl 1-n-propyl-4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate 
• 1423014-82-7 ethyl 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine-3-carboxylate 

Relevant articles and documents

Structural modifications to tetrahydropyridine-3-carboxylate esters en route to the discovery of M5-preferring muscarinic receptor orthosteric antagonists

The M5 muscarinic acetylcholine receptor is suggested to be a potential pharmacotherapeutic target for the treatment of drug abuse. We describe herein the discovery of a series of M5-preferring orthosteric antagonists based on the scaffold of 1,2,5,6-tetrahydropyridine-3- carboxylic acid. Compound 56, the most selective compound in this series, possesses an 11-fold selectivity for the M5 over M1 receptor and shows little activity at M2-M4. This compound, although exhibiting modest affinity (Ki = 2.24 μM) for the [3H]N-methylscopolamine binding site on the M5 receptor, is potent (IC50 = 0.45 nM) in inhibiting oxotremorine-evoked [3H]DA release from rat striatal slices. Further, a homology model of human M5 receptor based on the crystal structure of the rat M3 receptor was constructed, and docking studies of compounds 28 and 56 were performed in an attempt to understand the possible binding mode of these novel analogues to the receptor.