153322-05-5

Basic information

• Product Name: LaniceMine
• Synonyms: LaniceMine;2-PyridineethanaMine, a-phenyl-, (aS)-;(1S)-1-phenyl-2-pyridin-2-ylethanamine;(S)-1-phenyl-2-(pyridin-2-yl)ethanamine
• CAS NO: 153322-05-5
• Molecular Formula: C13H14N2
• Molecular Weight: 198.26366
• Mol File: 153322-05-5.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 307.7°Cat760mmHg
• Flash Point: 160.5°C
• Appearance: /
• Density: 1.097g/cm³
• Vapor Pressure: 0.000712mmHg at 25°C
• Refractive Index: 1.601
• Solubility: ≤20mg/ml in ethanol;30mg/ml in DMSO;5mg/ml in dimethyl formamide
• PKA: 8.29±0.10(Predicted)
• CAS DataBase Reference: LaniceMine(CAS DataBase Reference)
• NIST Chemistry Reference: LaniceMine(153322-05-5)
• EPA Substance Registry System: LaniceMine(153322-05-5)

Safety Data

• Hazardous Substances Data: 153322-05-5(Hazardous Substances Data)

Usage

Description

Lanicemine is a non-selective, voltage-dependent NMDA channel blocker (IC50 = 4-7 μM) that binds to sites within the channel pore with a Ki value of 0.56-2.1 μM. Compared to ketamine , lanicemine exhibits a lower propensity to be trapped within the NMDA channel (86% versus 54% trapping) following removal and reapplication of glutamate. It has been examined for its potential to produce antidepressant effects without adverse psychotomimetic activity.

Uses

Lanicemine is a non-selective voltage-dependant NMDA channel blocker. It is a potential anti-depressant which does not cause psychotomimetic activity. Potential anti-hypertensive agent.

in vitro

previous study with lanicemine and ketamine found that both compounds could bind with low-to-moderate affinity to sites within the nmda channel pore, exhibit strong voltage dependence, and have similar lack of nr2a vs nr2b subunit selectivity [1].

in vivo

in animal study, cortical eeg recordings were obtained from rats trained to perform an auditory detection task for food reward. results showed that both lanicemine and ketamine produced pronounced dose-dependent elevations in spontaneous gamma-band eeg, but only gamma changes for ketamine were tightly coupled to increases in locomotor activity, indicating that lanicemine not only engaged brain circuits involved in the generation of gamma-eeg, but also influenced these networks independent of the broader systemslevel disruptions typical of ketamine [1].

IC 50

4-7 μm

references

[1] g. sanacora, m. a. smith, s. pathak, et al. lanicemine: a low-trapping nmda channel blocker produces sustained antidepressant efficacy with minimal psychotomimetic adverse effects. molecular psychiatry 19(9), 978-985 (2014).

InChI:InChI=1/C13H14N2/c14-13(11-6-2-1-3-7-11)10-12-8-4-5-9-15-12/h1-9,13H,10,14H2