Aminophenols
![Medchemexpress LLC N-(4-hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide | 901770-40-9 | MFCD29037927 | 99.5% | C16H21N3O3S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261035.png-250.jpg)
Medchemexpress LLC N-(4-hydroxyphenyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide | 901770-40-9 | MFCD29037927 | 99.5% | C16H21N3O3S | 10MG
Biotin-4-aminophenol is a biotin-phenol analog used to generate biotinylated protein radicals for selective labeling of tyrosine residues in proteins. Supplied as a solid or as pre-dissolved 10 mM solutions in DMSO, it is intended for biochemical labeling and proteomics workflows where site-selective modification of proteins is required.
- Selective tyrosine labeling via radical-mediated conjugation.
- Efficient generation of biotinylated protein radicals for detection and enrichment.
- Available as solid or 10 mM solution in DMSO for experimental convenience.
- High purity suitable for biochemical and proteomics applications.
- White to off-white solid with good solubility in DMSO.
Medchemexpress LLC NPS-2143 hydrochloride | 324523-20-8 | MFCD16038896 | 100.0% | 445.38 g·mol⁻¹ | C24H26Cl2N2O2 | 10 MG
NPS-2143 hydrochloride is an orally active calcilytic agent and a selective, potent antagonist of the calcium-sensing receptor (CaSR). It inhibits CaSR-mediated increases in cytoplasmic Ca2+ (reported IC50 ≈ 43 nM) and is used as a research reagent for studies of CaSR signaling, pharmacology, and related cellular assays.
- Selective CaSR antagonist with reported IC50 ≈ 43 nM.
- High purity (≈99.98%).
- Solid, white to off-white powder suitable for laboratory use.
- Molecular weight 445.38 g·mol⁻¹; molecular formula C24H26Cl2N2O2.
- Recommended storage: 4°C sealed; in solvent -80°C (6 months), -20°C (1 month).
- Available in small research pack sizes (for example, 10 mg).
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
Medchemexpress LLC Pirmenol hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g·mol⁻¹ | C22H31ClN2O | 100 MG
Pirmenol hydrochloride is an orally active antiarrhythmic research compound used in pharmacology and electrophysiology studies. It inhibits IK.ACh currents by blocking muscarinic acetylcholine receptors and is provided as a high-purity solid for laboratory research use.
- Orally active compound suitable for cellular and in vivo studies.
- Reported to inhibit IK.ACh with IC50 ≈ 0.1 μM.
- High purity solid for reproducible experimental results.
- Available in small-quantity packages appropriate for research workflows.
- Intended for laboratory research; not for human or diagnostic use.
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.
eMolecules 3-Hydroxydiphenylamine | 101-18-8 | MFCD00002262 | 1g
Combi-Blocks | 3-Hydroxydiphenylamine | 1g | 290690778 | QD-5472 | 95.000 | 101-18-8 | MFCD00002262 | 185.226 | C12H11NO
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![eMolecules Medchem Express / S55746 / 5mg / 446260465 / HY-117288 / / 1448584-12-0 / [null] / 710.831 / C43H42N4O6](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502467473.JPG-250.jpg)
eMolecules Medchem Express / S55746 / 5mg / 446260465 / HY-117288 / / 1448584-12-0 / [null] / 710.831 / C43H42N4O6
Medchem Express / S55746 / 5mg / 446260465 / HY-117288 / / 1448584-12-0 / [null] / 710.831 / C43H42N4O6
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.
Medchemexpress LLC Ly266097 hydrochloride | 172895-39-5 | MFCD00949080 | >98.0% | 407.33 g·mol⁻¹ | C21H23ClN2O2 · HCl | 25 MG
LY266097 hydrochloride is the hydrochloride salt of LY-266,097, a potent and selective 5-HT2B receptor antagonist used as a research reagent in neuroscience and pharmacology. It is supplied as a crystalline solid, typically at high purity, and is used for receptor binding and functional studies in vitro and in vivo.
- Selective 5-HT2B receptor antagonist for neuroscience research.
- High purity (typically ≥98%) for analytical and biological assays.
- Available as powder or as a 10 mM solution in DMSO, in milligram-scale packs.
- Molecular weight ~407.33 g·mol⁻¹; empirical formula C21H23ClN2O2 · HCl.
- Suited for receptor binding, functional assays, and pharmacology studies.
Medchemexpress LLC Guvacine hydrochloride | 6027-91-4 | 99.9% | 163.60 g·mol⁻¹ | C6H10ClNO2 | 100 MG
Guvacine hydrochloride is a research reagent used to inhibit GABA uptake in neuropharmacology and biochemical studies. It is supplied as a white to off-white solid and is available in both solid and small-solution formats for in vitro experiments.
- Functions as a GABA uptake inhibitor for neuropharmacology research.
- High purity (~99.9%) minimizes impurities in assays.
- Available as solids and as a DMSO solution for experimental flexibility.
- White to off-white solid suitable for analytical and in vitro use.
- Molecular weight 163.60 g·mol⁻¹ supports accurate stoichiometry calculations.
Medchemexpress LLC ZK824190 hydrochloride | 2629177-12-2 | 99.2% | 450.86 g/mol | C22H21ClF2N2O4 | 10MM 1ML
ZK824190 hydrochloride is the hydrochloride salt of a selective, orally available urokinase plasminogen activator (uPA) inhibitor used in research into uPA biology and potential therapies for multiple sclerosis. It is supplied as a high-purity solid and as a pre-made 10 mM solution in DMSO for in vitro and preclinical studies; not for human use.
- Selective urokinase plasminogen activator (uPA) inhibitor.
- Supplied as 10 mM solution in DMSO and as solid quantities.
- High purity suitable for research applications.
- Molecular formula: C22H21ClF2N2O4.
- Molecular weight: 450.86 g/mol.
- CAS: 2629177-12-2 for substance identification.
- Provided as the hydrochloride salt for stability and handling.
- Intended for in vitro and preclinical research only, not for human use.
eMolecules Medchem Express / OTS964 (hydrochloride) / 5mg / 446261301 / HY-12467 / / 1338545-07-5 / MFCD28386220 / 428.980 / C23H25ClN2O2S
Medchem Express / OTS964 (hydrochloride) / 5mg / 446261301 / HY-12467 / / 1338545-07-5 / MFCD28386220 / 428.980 / C23H25ClN2O2S
Medchemexpress LLC HLCL-61 hydrochloride | 1158279-20-9 | MFCD09446681 | 99.9% | 380.91 g/mol | C23H25ClN2O | 25 MG
HLCL-61 hydrochloride is a research-grade small-molecule inhibitor of protein arginine methyltransferase 5 (PRMT5), supplied as a hydrochloride salt for laboratory use only. It is intended for in vitro and preclinical research and is not for human or veterinary use.
- Inhibits PRMT5 activity in biochemical and cellular assays.
- High reported purity of 99.87%.
- Molecular weight is 380.91 g/mol.
- Identified by CAS number 1158279-20-9 for unambiguous chemical identification.
- Available in milligram quantities suitable for laboratory studies, including a 25 mg pack size.
Medchemexpress LLC Triacetonamine (2,2,6,6-tetramethyl-4-piperidone) | 826-36-8 | MFCD00005975 | 155.24 | 1000 G
Triacetonamine is utilized as an intermediate in the synthesis of pharmaceutical products, pesticides, and photostabilizers for polymers. It exhibits oral activity and can induce acute liver failure (ALF) in rats.
- Used as an intermediate for the synthesis of pharmaceutical products, pesticides, and photostabilizers for polymers
- Has oral activity
- Can induce acute liver failure (ALF) in rats
Medchemexpress LLC Thiethylperazine dimaleate | 1179-69-7 | 100.0% | 1 ML
Thiethylperazine dimaleate is a phenothiazine derivative that acts as an orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist. It is also a selective ABCC1 activator that reduces amyloid-β (Aβ) load in mice. This compound exhibits anti-emetic, antipsychotic, and antimicrobial effects.
- Phenothiazine derivative
- Orally active and potent dopamine D2-receptor and histamine H1-receptor antagonist
- Selective ABCC1 activator
- Reduces amyloid-β (Aβ) load in mice
- Exhibits anti-emetic, antipsychotic, and antimicrobial effects