Aminophenols
eMolecules 14452-34-7 | 2,4-Dimethyl-6-nitrophenol | MFCD00191633 | 1g
Ambeed | 2-(4-(Trifluoromethoxy)phenyl)ethanol | 1g | 525055889 | A145273 | 196811-90-2 | MFCD08276850 | 206.164 | C9H9F3O2
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Medchemexpress LLC CSRM617 hydrochloride | 1353749-74-2 | 100.0% | 100 MG
CSRM617 hydrochloride is the hydrochloride salt of a selective small-molecule inhibitor of the transcription factor ONECUT2, supplied as a white to off-white solid for research use.
- Selective inhibitor of ONECUT2 transcription factor.
- Hydrochloride salt, white to off-white solid.
- Purity 99.97%.
- Molecular weight 291.69 g/mol.
- Soluble in DMSO (100 mg/mL; ultrasonic assistance recommended).
- Store sealed, away from moisture; in solvent: -80°C (6 months), -20°C (1 month).
- For research use only; not for human use.
Medchemexpress LLC BN82002 hydrochloride | 1049740-43-3 | 99.4% | 395.88 | 50 MG
BN82002 hydrochloride is a potent, selective, and irreversible inhibitor of the CDC25 phosphatase family. It inhibits CDC25A, CDC25B2, CDC25B3, CDC25C, and 25C-cat with IC50 values of 2.4, 3.9, 6.3, 5.4, and 4.6 μM, respectively. The compound demonstrates approximately 20-fold greater selectivity over CD45 tyrosine phosphatase and inhibits cell proliferation in several human tumor cell lines in a concentration-dependent manner in the low micromolar range. Treatment with 50 μM BN82002 modestly affects cell cycle distribution, suggesting cell cycle arrest at various stages.
- Potent, selective, and irreversible inhibitor of CDC25 phosphatase family.
- Displays approximately 20-fold greater selectivity over CD45 tyrosine phosphatase.
- Inhibits cell proliferation in various human tumor cell lines.
- For research use only.
Medchemexpress LLC Imiloxan hydrochloride | 81167-22-8 | 98.5% | 280.75 g/mol | C14H17ClN2O2 | 5 MG
Imiloxan hydrochloride is a potent, selective α2B-adrenoceptor antagonist used in pharmacological research to probe α2-adrenergic receptor subtype function. It is supplied as a characterized solid with defined purity and molecular weight for use in receptor-binding studies, in vitro assays, and in vivo experiments.
- Selective α2B-adrenoceptor antagonist
- High purity suitable for research applications
- Supplied in small research pack sizes for lab use
- Supported by analytical data (HNMR, LC-MS)
- Provided with SDS, COA, and handling instructions
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 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 Sotalol hydrochloride | 959-24-0 | 99.9% | 100 MG
Sotalol hydrochloride (MJ 1999) is an orally active, non-selective β-adrenergic receptor blocker and a potent antiarrhythmic agent. It can be used for the research of pediatric arrhythmias and also functions as an antiepileptic agent.
- Blocks β-receptors
- Blocks potassium KCNH2 channels
- Suitable for research on pediatric arrhythmias
- Functions as an antiepileptic agent
Medchemexpress LLC Bestatin-d7 (hydrochloride) | 97.7% | 1 MG
Bestatin-d7 (hydrochloride) is a deuterium-labeled version of Bestatin (hydrochloride). Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, primarily utilized in cancer research.
- Deuterium labeled compound
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase
Medchemexpress LLC SAR7334 hydrochloride | 1333207-63-8 | 98.0% | 440.79 g/mol | C21H24Cl3N3O | 10 MG
SAR7334 hydrochloride is the hydrochloride salt of SAR7334, a potent and selective small-molecule inhibitor of the TRPC6 ion channel. It inhibits TRPC6 currents with an IC50 of 7.9 nM and is supplied as a high-purity research reagent for biochemical and cellular studies.
- Potent TRPC6 inhibitor (IC50 7.9 nM).
- Hydrochloride salt form for improved stability and solubility.
- Purity: 98.0% (as supplied).
- Molecular weight: 440.79 g/mol.
- Available as milligram quantities and as a 10 mM solution in DMSO.
- Intended for research use only; not for human or clinical use.
Medchemexpress LLC PKI-179 hydrochloride | 1463510-35-1 | 99.66% | 525.00 | 10 MG
PKI-179 hydrochloride is a potent and orally active dual PI3K/mTOR inhibitor. It exhibits activity over various PI3K isoforms and mTOR, along with E545K and H1047R. This compound demonstrates anti-tumor activity in vivo.
- Potent and orally active dual PI3K/mTOR inhibitor
- Inhibits PI3K-α, PI3K-β, PI3K-γ, PI3K-δ and mTOR
- Shows activity over E545K and H1047R
- Exhibits anti-tumor activity in vivo
Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | 99.9% | 5 MG
Sotalol hydrochloride (MJ 1999) is an orally active, non-selective β-adrenergic receptor blocker. It is a potent antiarrhythmic agent used for the research of pediatric arrhythmias.
- Orally active, non-selective β-adrenergic receptor blocker
- Potent antiarrhythmic agent
- Blocks β-receptors and potassium KCNH2 channels
- Suitable for research on pediatric arrhythmias
- Classified as an antiepileptic agent
Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | MFCD00242937 | 99.9% | 308.82 g/mol | C12H21ClN2O3S | 10 MG
Sotalol hydrochloride is an orally active, non-selective β-adrenergic receptor blocker with class III antiarrhythmic activity used in cardiovascular and electrophysiology research. It is supplied as a characterized research chemical with high purity and documented analytical data.
- High purity as determined by LCMS (≈99.9%).
- Molecular weight 308.82 g/mol and molecular formula C12H21ClN2O3S.
- Used to study β-receptor blockade and cardiac repolarization (potassium channel) effects.
- Supplied in small research pack sizes and solution formats (for example, 10 MG solid or 10 mM/1 mL solution).
![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127359.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 6mg | 564356415