Aminophenols
Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | 99.9% | 50 MG
Sotalol hydrochloride is an orally active, non-selective β-adrenergic receptor blocker. It functions as a potent antiarrhythmic agent suitable for research on pediatric arrhythmias. It blocks β-receptors and potassium KCNH2 channels, and is also identified as an Antiepileptic Agent.
- Orally active
- Non-selective β-adrenergic receptor blocker
- Potent antiarrhythmic agent
- Blocks β-receptors and potassium KCNH2 channels
- Antiepileptic agent
- In vivo effects up to 100 mg/kg do not impact electroconvulsive threshold
- Does not interfere with antielectroshock action of several antiepileptic drugs at 80-100 mg/kg
- Does not impair motor performance or long-term memory when used alone or in combination with antiepileptics
![eMolecules 873-55-2 | Sodium benzenesulfinate | Ambeed | MFCD00013135 | 164.150 | C6H5NaO2S | 95.000 | [Na+].[O-]S(=O)c1ccccc1 | 10g | 525029262](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502426537.PNG-250.jpg)
eMolecules 873-55-2 | Sodium benzenesulfinate | Ambeed | MFCD00013135 | 164.150 | C6H5NaO2S | 95.000 | [Na+].[O-]S(=O)c1ccccc1 | 10g | 525029262
Sodium benzenesulfinate | Ambeed | 873-55-2 | MFCD00013135 | 164.150 | C6H5NaO2S | 95.000 | [Na+].[O-]S(=O)c1ccccc1 | 10g | 525029262
Ambeed 2Methoxy6 trifluoromethoxy ph
(2-Methoxy-6-(trifluoromethoxy)phenyl)boronic acid, 309977-92-2, 95%
Cayman Chemical N-acetyl-2-AmInophenol 50g
A derivative of acetaminophen; inhibits ADP- or arachidonic acid-induced platelet aggregation in isolated human platelet-rich plasma at 50 µM; decreases disease severity and prevents increases in paw volume in a rat model of collagen-induced arthritis at 1 mg/kg; has been used as a synthetic intermediate in the synthesis of compounds with antimalarial activity; a potential impurity in commercial preparations of acetaminophen
TARGETMOL CHEMICALS INC SPECNUEZHENIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Specnuezhenide (Nuezhenide) significantly protects human neuroblastoma SH-SY5Y cells from 6-hydroxydopamine-induced neurotoxicity.Nuezhenide is the main inhibitory compound of fruits it shows a clear inhibitory effect to the seeds of wheat and Chinese cabbage. purity: 99%
Medchemexpress LLC Biotin-4-aminophenol | 901770-40-9 | 99.45% | C16H21N3O3S | 50 MG
Biotin-4-aminophenol is a biotin-phenol analog that generates free radicals and conjugates to tyrosine residues in proteins more efficiently and selectively than the previously reported BP1. It is intended for research use only.
- Generates free radicals and conjugates to tyrosine residues in proteins.
- More efficient and selective than previously reported BP1.
- Suitable for spatiotemporal profiling of cytosolic signaling complexes in living cells.
- Can be used with 500 µM working solution for cell incubation.
- Proximity labeling reaction is triggered by H2O2.
- Reaction can be quenched using a specific buffer.
- Supports analysis of digested peptides by nano LC-MS/MS.
Medchemexpress LLC Quercetagitrin | 548-75-4 | 50 MG
Quercetagitrin, a natural product from African marigold, exhibits anti-inflammatory activity. It shows promise in neuroscience research by inhibiting Tau accumulation, reversing neuroinflammation, and improving cognitive function in P301S-Tau transgenic mouse models. This compound also acts as a dual-target inhibitor of PTPN6 and PTPN9, enhancing glucose uptake in C2C12 myoblasts, making it a relevant agent for studies in Alzheimer's disease and type 2 diabetes.
- Exhibits anti-inflammatory activity.
- Inhibits Tau accumulation and reverses neuroinflammation.
- Acts as a dual-target inhibitor of PTPN6 and PTPN9.
- Enhances glucose uptake and mitigates insulin resistance in C2C12 myoblasts.
- Attenuates synaptic impairments and cognitive deficits in P301S-Tau transgenic mice.
- Reduces tau accumulation and gliosis.
- Applicable for research in Alzheimer's disease and type 2 diabetes.
Medchemexpress LLC Benzyltriethylammonium chloride | 56-37-1 | MFCD00011824 | ≥98.0% | 227.77 g·mol⁻¹ | C13H22ClN | 1000g
Benzyltriethylammonium chloride is a quaternary ammonium salt commonly used as a phase transfer catalyst surfactant and stabilizer in various chemical reactions especially in organic synthesis Benzyltriethylammonium chloride has unique chemical properties that facilitate the transfer of ions or molecules from one phase to another making it an important ingredient in a variety of industrial processes
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.
=O | 5g | 205388951](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00128114-205388951.PNG-250.jpg)
eMolecules 2-Amino-4-chloro-5-nitrophenol | Combi-BlocksMFCD00010300 | 188.570 | C6H5ClN2O3 | 98.000 | Nc1cc(Cl)c(cc1O)[N+]([O-])=O | 5g | 205388951
2-Amino-4-chloro-5-nitrophenol | Combi-BlocksMFCD00010300 | 188.570 | C6H5ClN2O3 | 98.000 | Nc1cc(Cl)c(cc1O)[N+]([O-])=O | 5g | 205388951
Medchemexpress LLC NS8593 hydrochloride | 875755-24-1 | 99.76% | 299.80 | 1 MG
NS8593 hydrochloride is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels). It reversibly inhibits SK3-mediated currents with a Kd value of 77 nM. NS8593 hydrochloride inhibits all SK1-3 subtypes in a Ca2+-dependent manner (Kds of 0.42, 0.60, and 0.73 μM, respectively, at 0.5 μM Ca2+), but does not affect intermediate and large conductance Ca2+-activated K+ channels (hIK and hBK channels, respectively). It is for research use only and not sold to patients.
- Potent and selective small conductance Ca2+-activated K+ channels inhibitor
- Reversibly inhibits SK3-mediated currents with a Kd value of 77 nM
- Inhibits SK1-3 subtypes Ca2+-dependently
- Does not affect intermediate and large conductance Ca2+-activated K+ channels
- Affects firing rate and firing pattern of dopaminergic neurons in vivo in C57Bl/6 mice at doses of 3 and 10 mg/kg intravenously