Aminophenols
![Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl-, hydrochloride | 61477-94-9 | MFCD01691662 | 99.3% | 374.95 g/mol | C22H31ClN2O | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000213420.png-250.jpg)
Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl-, hydrochloride | 61477-94-9 | MFCD01691662 | 99.3% | 374.95 g/mol | C22H31ClN2O | 1 ML
Pirmenol hydrochloride is an antiarrhythmic research compound supplied for laboratory use as a 10 mM solution in DMSO (1 mL) or as a solid with solvent. It inhibits IK.ACh and is intended for preclinical cardiovascular and ion-channel research. The material is characterized by high purity and is accompanied by a certificate of analysis.
- Provided as 10 mM in DMSO, 1 mL stock solution or solid plus solvent
- High purity, 99.3%
- Molecular formula C22H31ClN2O; molecular weight 374.95 g/mol
- CAS number 61477-94-9
- Storage: solid at 4°C under nitrogen; in solvent -80°C for 6 months, -20°C for 1 month
- Suitable for cardiovascular and ion-channel research applications
Medchemexpress LLC Riluzole hydrochloride | 850608-87-6 | 99.9% | 500 MG
Riluzole hydrochloride is an anticonvulsant agent that functions as a use-dependent Na+ channel blocker and can also inhibit GABA uptake with an IC50 of 43 μM. It is intended for research use only and not sold to patients.
- Acts as an anticonvulsant agent.
- Inhibits Na+ channels.
- Can inhibit GABA uptake.
Medchemexpress LLC Benzamide, 4-fluoro-N-[2-[4-(7-methoxy-1-naphthalenyl)-1-piperazinyl]ethyl]-,hydrochloride | 286369-38-8 | 99.9% | 443.94 | 25 MG
S-14506 hydrochloride is a potent 5-HT1A agonist and a 5-HT2A/2C antagonist. It also exhibits dopamine antagonist properties by blocking dopamine D2 receptors. This compound inhibits the in vivo binding of [3H]raclopride in striatum and olfactory bulbs, with potential for research as an anxiolytic agent.
- Potent 5-HT1A agonist.
- 5-HT2A/2C antagonist.
- Displays dopamine antagonist properties by blocking dopamine D2 receptors.
- Inhibits the in vivo binding of [3H]raclopride in striatum and olfactory bulbs.
- Potential for the research of anxiolytic agents.
