Aminophenols
Medchemexpress LLC Rs 17053 hydrochloride | 169505-93-5 | MFCD09971032 | 99.9% | 449.41 | C24H30Cl2N2O2 | 50 MG
RS 17053 hydrochloride is a research-grade small molecule that functions as a potent, selective α1A adrenoceptor antagonist for pharmacological studies. Supplied as a solid with high purity, it includes manufacturer-specified solubility, formulation, and storage guidance for both in vitro and in vivo use.
- Potent, selective α1A adrenoceptor antagonist (pKi 9.1; pA2 9.8).
- High purity: 99.9%.
- Solid form, white to off-white.
- Soluble in DMSO (~100 mg/mL); ultrasonic assistance recommended.
- Compatible with multiple in vivo formulations at ≥2.08 mg/mL for clear solutions.
- Stable with recommended storage: sealed at 4°C; in solution -80°C for long-term.
Medchemexpress LLC Fasudil hydrochloride | 105628-07-7 | MFCD00943198 | 100.0% | 327.83 g/mol | C14H18ClN3O2S | 100 MG
Fasudil hydrochloride is the hydrochloride salt of fasudil, a nonspecific RhoA/ROCK inhibitor used in research to investigate Rho-kinase-mediated signaling and kinase activity. It has CAS 105628-07-7, molecular formula C14H18ClN3O2S, and a molecular weight of 327.83 g/mol. The compound is supplied as a high-purity research reagent and is soluble in water and DMSO at the concentrations indicated on the product datasheet.
- Nonspecific RhoA/ROCK inhibitor for biochemical and cellular studies.
- Hydrochloride salt form for improved aqueous solubility.
- High purity (99.97%) suitable for research applications.
- Molecular weight 327.83 g/mol; formula C14H18ClN3O2S.
- Solubility: H2O 55 mg/mL (requires ultrasonic), DMSO ≥ 31 mg/mL.
- Intended for research use only; not for human or clinical use.
![Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g/mol | C22H31ClN2O | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000213617.png-250.jpg)
Medchemexpress LLC 2-pyridinemethanol, α-[3-[(2R,6S)-2,6-dimethyl-1-piperidinyl]propyl]-α-phenyl hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g/mol | C22H31ClN2O | 50 MG
Pirmenol hydrochloride is the hydrochloride salt of pirmenol, an orally active antiarrhythmic compound used in cardiovascular research to study cardiac arrhythmias and ion channel modulation. It acts on muscarinic acetylcholine receptors to inhibit IK.ACh and is supplied as a solid for laboratory use.
- Orally active antiarrhythmic compound used in research.
- Inhibits IK.ACh by blocking muscarinic acetylcholine receptors (IC50 ~0.1 μM).
- Provided as a white to yellow solid suitable for biochemical assays.
- High reported purity (~98.8%) for analytical and pharmacology studies.
- Recommended storage: solid at 4°C under inert gas; solutions at -20°C to -80°C.
Medchemexpress LLC LMP744 hydrochloride | 308246-57-3 | 488.92 | 1 ML
LMP744 hydrochloride (MJ-III65 hydrochloride) is a DNA intercalator and Topoisomerase I (Top1) inhibitor with antitumor activity. It is intended for research use only.
- Dose-dependent accumulation of cells in the S and G2 phases of the cell cycle
- Antiproliferative activity against various human cell lines
- Moderately active against human A253 and FaDu tumor xenografts in nude mice
Medchemexpress LLC CWI1-2 hydrochloride | 2408590-37-2 | C22H18Cl4N6O3 | 25 MG
CWI1-2 hydrochloride is an IGF2BP2 inhibitor that binds IGF2BP2 and inhibits its interaction with m6A-modified target transcripts. It induces apoptosis and differentiation, and demonstrates promising anti-leukemic effects. It is intended for research use only.
- Binds IGF2BP2
- Inhibits interaction with m6A-modified target transcripts
- Induces apoptosis
- Induces differentiation
- Demonstrates anti-leukemic effects
- For research use only
eMolecules 28165-60-8 | 2,3-DICHLORO-6-NITROPHENOL | MFCD08458821 | 1g
Ambeed | 2-Bromo-3-hexylthiophene | 5g | 525081498 | A165359 | 69249-61-2 | MFCD09907959 | 247.190 | C10H15BrS
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Medchemexpress LLC NPS-2143 hydrochloride | 324523-20-8 | MFCD16038896 | 100.0% | 445.4 g/mol | C24H26Cl2N2O2 | 1 MG
NPS-2143 hydrochloride is an orally active calcilytic agent that acts as a selective and potent antagonist of the calcium-sensing receptor (CaSR). Supplied as a high-purity solid for research use, it is used in biochemical and cellular studies to probe CaSR-mediated signaling and parathyroid hormone regulation.
- Selective calcium-sensing receptor antagonist for targeted research applications.
- High purity suitable for biochemical and cellular assays.
- Solid form for convenient storage and handling.
- Small research-scale quantity for assay development and proof-of-concept studies.
Medchemexpress LLC Sotalol hydrochloride | 959-24-0 | MFCD00870503 | ≥99.0% | 200 MG
Sotalol hydrochloride is an orally active, non-selective β-adrenergic receptor blocker and a potent antiarrhythmic agent. It is suitable for research on pediatric arrhythmias and also functions as an antiepileptic agent. This compound works by blocking β-receptors and potassium KCNH2 channels.
- Orally active, non-selective β-adrenergic receptor blocker
- Potent antiarrhythmic agent
- Can be used for research of pediatric arrhythmias
- Blocks β-receptors
- Blocks potassium KCNH2 channels
- Functions as an antiepileptic agent
- Target for adrenergic receptor and potassium channel research
- Relevant for cardiovascular disease and neurological disease research
- Stable under recommended storage conditions
- Available as a solid
Medchemexpress LLC Mt-7716 hydrochloride | 1215859-93-0 | MFCD07778657 | 99.1% | 477.00 g·mol⁻¹ | C27H29ClN4O2 | 100 MG
MT-7716 hydrochloride is a selective non-peptide nociceptin receptor (NOP) agonist supplied as the hydrochloride salt for research use. It is investigated for reducing alcohol-seeking behavior and relapse, and is provided as a solid reagent for in vitro and in vivo pharmacology studies.
- Selective non-peptide nociceptin (NOP) receptor agonist.
- Investigated for reduction of alcohol seeking and relapse prevention.
- Provided as the hydrochloride salt in solid form for research applications.
- High purity (≈99.1%) suitable for analytical and pharmacology studies.
- Molecular formula C27H29ClN4O2, molecular weight 477.00 g·mol⁻¹.
- Storage: 4°C sealed, away from moisture; in solvent, -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Hypidone hydrochloride | 1339058-04-6 | 99.7% | 334.84 g/mol | C18H23ClN2O2 | 100 MG
Hypidone hydrochloride is the hydrochloride salt of a research compound with potent serotonergic activity. It functions as a selective serotonin (5-HT) uptake inhibitor and a 5-HT1A receptor agonist, and has demonstrated oral activity in animal models of depression. Supplied as a powder for laboratory research use only; not for human or clinical use.
- High purity suitable for research applications.
- Dual mechanism: serotonin uptake inhibition and 5-HT1A receptor agonism.
- Demonstrated oral activity in animal depression models.
- Available in multiple pack sizes including small research quantities.
- Recommended sealed storage away from moisture; in solvent store at -80°C for long term.
Medchemexpress LLC MRL-494 hydrochloride | 2699937-04-5 | 98.6% | 1 MG
MRL-494 hydrochloride is an antibacterial agent that functions as an inhibitor of β-barrel assembly machine A (BamA), remaining impervious to efflux and the outer membrane permeability barrier. It effectively inhibits both Gram-positive and Gram-negative bacteria by lethally disrupting the cytoplasmic membrane and inhibiting Outer Membrane Proteins (OMPs) biogenesis.
- Antibacterial agent
- Inhibitor of β-barrel assembly machine A (BamA)
- Impervious to efflux and the outer membrane permeability barrier
- Inhibits gram-positive bacteria
- Inhibits gram-negative bacteria
- Lethally disrupts the cytoplasmic membrane
- Inhibits outer membrane proteins (OMPs) biogenesis
Medchemexpress LLC Ozanimod hydrochloride | 1618636-37-5 | 98.1% | 10 MG
Ozanimod hydrochloride is the hydrochloride salt of ozanimod (RPC-1063), a selective sphingosine 1-phosphate (S1P) receptor modulator supplied for laboratory research use only. It is used in studies of immune modulation and relapsing multiple sclerosis.
- Purity 98.1%.
- Molecular weight 440.92.
- Molecular formula C23H25ClN4O3.
- White to off-white solid; also available as 10 mM solution in DMSO.
- Storage: 4°C sealed; in solvent: -80°C (6 months), -20°C (1 month).
- Intended for laboratory research on S1P receptor biology and multiple sclerosis models.
Medchemexpress LLC CWI1-2 hydrochloride | 2408590-37-2 | C22H18Cl4N6O3 | 5 MG
CWI1-2 hydrochloride is an IGF2BP2 inhibitor that binds IGF2BP2 and inhibits its interaction with m6A-modified target transcripts, induces apoptosis and differentiation, and shows promising anti-leukemic effects.
- IGF2BP2 inhibitor.
- Inhibits IGF2BP2 interaction with m6A-modified target transcripts.
- Induces apoptosis and differentiation.
- Demonstrates anti-leukemic effects.
- Effective in reducing Gln uptake and impairing mitochondrial function in AML cells.
- Inhibits colony-forming ability of leukemic mouse blasts.
- Impairs self-renewal of LSC/LIC.
- Delays leukemia onset and prolongs survival in vivo.
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