Aminophenols
Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | 99.9% | 500 MG
Sotalol hydrochloride is an orally active, non-selective β-adrenergic receptor blocker. It is a potent antiarrhythmic agent used for the research of pediatric arrhythmias. This compound blocks β-receptors and potassium KCNH2 channels, and acts as an antiepileptic agent.
- Orally active
- Non-selective β-adrenergic receptor blocker
- Potent antiarrhythmic agent
- Used for the research of pediatric arrhythmias
- Blocks β-receptors
- Blocks potassium KCNH2 channels
- Acts as an antiepileptic agent
![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 20mg | 564356420](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000128174.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 20mg | 564356420
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 20mg | 564356420
Medchemexpress LLC Scopine hydrochloride | 85700-55-6 | 99.7% | 5 MG
Scopine hydrochloride, also known by its synonym 6,7-Epoxytropine hydrochloride, is recognized as a metabolite of Scopolamine and functions as a brain-targeting compound. This compound has demonstrated the ability to significantly elevate the brain exposure of Chlorambucil and consequently amplify its anti-glioma activity. These properties make Scopine hydrochloride a candidate for targeted therapy research focused on brain gliomas.
- It is a metabolite of Scopolamine.
- It acts as a brain-targeting compound.
- It significantly increases the brain exposure of Chlorambucil.
- It enhances the anti-glioma activity of Chlorambucil.
- It is used in targeted therapy research for brain gliomas.
- CHLS (Scopine combined with Chlorambucil) exhibits significant anti-glioma activity in C6 cells.
- Its IC50 & target is the α adrenergic receptor.
Medchemexpress LLC Oxprenolol-d7 hydrochloride | 1189649-47-5 | 98.3% | 308.85 | C15H17D7ClNO3 | 10 MG
Oxprenolol-d7 hydrochloride is a deuterium-labeled hydrochloride salt of oxprenolol used as an analytical standard and internal standard for LC-MS and other quantitative assays. Supplied at high purity in mg-scale packages, follow recommended cold storage to preserve stability.
- Deuterium-labeled hydrochloride salt for use as an analytical/internal standard.
- High purity (98.25%) for accurate quantitation.
- Available in mg-scale packages to support method development.
- Recommended storage: powder -20°C (3 years) or 4°C (2 years).
- Molecular formula C15H17D7ClNO3 and molecular weight 308.85 for identification.
Medchemexpress LLC A 85380 hydrochloride | 174740-86-4 | ≥97.0% | 237.13 | 50 MG
A 85380 hydrochloride is a novel, high affinity neuronal nicotinic acetylcholine receptor (nAChR) agonist. It exhibits selectivity for the α4β2 nAChR subtypes and has a broad-spectrum analgesic profile.
- Novel, high affinity neuronal nicotinic acetylcholine receptor (nAChR) agonist.
- Selectivity for the α4β2 nAChR subtypes.
- Broad-spectrum analgesic profile.
- For research use only.
Medchemexpress LLC DC-Chol hydrochloride | 166023-21-8 | >99.9% | 537.26 | 250 MG
DC-Chol hydrochloride is a cationic lipid that inhibits Aβ40 fibril formation and amyloidogenesis of oxidized hCT. It enhances the body's immune response to antigens by inducing the production of Th1 (IL-2 and IFN-γ) and Th2 (IL-5) cytokines. This compound is also utilized as a gene delivery vector.
- Can inhibit Aβ40 fibril formation
- Strongly inhibits amyloidogenesis of oxidized hCT in a dose-dependent manner
- Induces production of Th1 (IL-2 and IFN-γ) and Th2 (IL-5) cytokines
- Enhances the body's immune response to antigens
- Used as a gene delivery vector
- Can be used in research for hepatitis B vaccines to improve vaccine immunity
Medchemexpress LLC Bis(2-cyanoethyl) diisopropylphosphoramidite | 102690-88-0 | 95.0% | 271.30 | 5 G
Bis(2-cyanoethyl) diisopropylphosphoramidite is a phosphoramidite monomer used in the synthesis of oligonucleotides. It is for research use only and not sold to patients.
Medchemexpress LLC Riluzole hydrochloride | 850608-87-6 | 99.87% | 1 G
Riluzole hydrochloride is an anticonvulsant agent that acts as a use-dependent Na+ channel blocker. It can also inhibit GABA uptake with an IC50 of 43 μM.
- Anticonvulsant agent
- Use-dependent Na+ channel blocker
- Can inhibit GABA uptake
- Inhibits peak autaptic IPSCs and prolongs IPSCs at 20 μM
- Causes a strong, concentration-dependent, readily reversible enhancement of responses to 2 μM GABA
Apexbio Technology LLC Clemizole hydrochloride 1163-36-6 10mM (in 1mL DMSO)
Clemizole hydrochloride is a histamine H1 receptor antagonist reported to inhibit hepatitis C virus (HCV) replication by targeting the viral NS4B protein a component essential for viral RNA replication Clemizole demonstrates antiviral activity in vitro against HCV genotype 2a subgenomic replicons exhibiting an IC50 value around 8 mM When combined with HCV protease inhibitors (such as VX950 or SCH503034) clemizole displays synergistic antiviral effects In contrast additive antiviral effects occur in combination with interferon ribavirin or polymerase inhibitors Clemizole is utilized in research contexts aimed at evaluating its efficacy potential antiviral combinations metabolism pathways and pharmacokinetics relevant to its consideration as a therapeutic candidate for HCV infection
Medchemexpress LLC 4-Piperidinecarboxamide, N-hydroxy-1-(2-methoxyethyl)-4-[[4-[4-(trifluoromethoxy)phenoxy]phenyl]sulfonyl]-, hydrochloride (1:1) | 226395-93-3 | 99.4% | 554.96 | 10 MG
SD-2590 hydrochloride is a potent MMP inhibitor with IC50 values of <0.1, <0.1, 0.18, and 1.7 nM for MMP2, MMP13, MMP9, and MMP8, respectively. It inhibits dilation of the left ventricle in rats. This product is for research use only.
- Potent MMP inhibitor
- Inhibits dilation of the left ventricle in rats
- Solid appearance
- White to off-white color
- Ships at room temperature
- Store at -20°C, sealed, away from moisture
- Soluble in DMSO at 55.5 mg/mL
Medchemexpress LLC DiAzKs hydrochloride | 2421187-79-1 | 98.0% | 100 MG
DiAzKs hydrochloride, also known as H-L-Photo-lysine hydrochloride, is a diazirine-containing lysine amino acid and a photo-cross-linker. It can be site-selectively incorporated into proteins and is used to crosslink protein-protein interactions in vitro and in living cells. This compound acts as a UV light-activated photo-crosslinking probe.
- Site-selective incorporation into proteins.
- Used to crosslink protein-protein interactions in vitro and in living cells.
- Acts as a UV light-activated photo-crosslinking probe.
- Photo-lysine can capture and identify proteins that recognize lysine post-translational modifications (PTMs), including 'readers' and 'erasers' of histone modifications.
![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 30mg | 564356422](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127648.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 30mg | 564356422
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 30mg | 564356422
Cayman Chemical N-acetyl-2-AmInophenol 250g
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
Medchemexpress LLC HY-117288A 5mg Medchemexpress, S55746 (hydrochloride) CAS:1448525-91-4 Purity:>98%
Medchemexpress, HY-117288A 5mg S55746 (hydrochloride) CAS:1448525-91-4 S55746 hydrochloride (BCL201 hydrochloride) is a potent, orally active and selective BCL-2 inhibitor, with a Ki of 1.3 nM and a Kd of 3.9 nM. S55746 hydrochloride (BCL201 hydrochloride) has antitumor activity with low toxicity. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.