Aminophenols
Medchemexpress LLC RS100329 hydrochloride (2,4(1H,3H)-pyrimidinedione derivative) | 1215654-26-4 | 99.6% | 462.89 | C20H26ClF3N4O3 | 1 ML
RS100329 hydrochloride is a potent, selective α1A-adrenoceptor antagonist provided for in vitro receptor pharmacology and biochemical assays. It is available as a pre-made 10 mM solution in DMSO (1 mL) and in multiple solid sizes, with accompanying analytical documentation for research use.
- Potent, selective α1A-adrenoceptor antagonist suitable for in vitro studies.
- Available as 10 mM DMSO solution (1 mL) and as solid in multiple mg sizes.
- High purity (99.57%) appropriate for biochemical assays.
- Molecular weight 462.89 and formula C20H26ClF3N4O3.
- Supplied with data sheet, certificate of analysis, and safety data sheet.
- Intended for research use; follow laboratory safety and SDS guidance.
Medchemexpress LLC Bepridil hydrochloride | 68099-86-5 | MFCD00868313 | 99.8% | 403.0 g/mol | C24H35ClN2O | 50 MG
Bepridil hydrochloride is the mono-hydrochloride salt of bepridil, a non-selective calcium channel blocker with antianginal activity. This product is offered as an analytical standard for research and analytical applications.
- Calcium channel blocker, with antianginal activity.
- Intended for research and analytical use.
- High purity (reported ≈99.8%).
- Hydrochloride salt form for increased solubility in polar solvents.
- Chemical formula: C24H35ClN2O; molecular weight: 403.0 g/mol; CAS: 68099-86-5.
Medchemexpress LLC R 59-022 hydrochlori 10mg | 93076-98-3 | 10MG
R 59-022 (DKGI-I) hydrochloride is a DGK inhibitor (IC50 2 8 M) R 59-022 hydrochloride inhibits the phosphorylation of OAG to OAPA R 59-022 hydrochloride is a 5-HT Receptor antagonist and activates protein kinase C (PKC) R 59-022 hydrochloride potentiates thrombin-induced diacylglycerol production in platelets and inhibits phosphatidic acid production in neutrophils[1 [2 [3 [4
Medchemexpress LLC Orotic acid hydrate | 50887-69-9 | MFCD00149398 | 99.3% | 174.11 g/mol | C5H6N2O5 | 100 G
Orotic acid hydrate (2,6-dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid hydrate) is an endogenous metabolite provided for research use. It is supplied as a solid and as a 10 mM solution in DMSO, and is available in multiple pack sizes including a 100 g solid. The compound is listed with CAS 50887-69-9 and a reported purity of 99.32%.
- High purity (99.32%) for analytical and biochemical applications.
- Available as solid and 10 mM DMSO solution for flexible use.
- Supplied with data sheet, COA, SDS, and LCMS report.
- Suitable as a reference standard or reagent in metabolic studies.
- Soluble in DMSO for easy formulation and handling.
Medchemexpress LLC Aminoiminomethanesulphinic acid | 1758-73-2 | MFCD00002397 | 99.1% | 108.12 g/mol | CH4N2O2S | 1000 G
Aminoiminomethanesulphinic acid (thiourea dioxide) is an organosulfur compound supplied for research and analytical use. It functions as a reducing agent and reagent in biochemical assays and industrial processes. The white to off-white solid has CAS 1758-73-2, molecular formula CH4N2O2S, and a molecular weight of 108.12 g/mol.
- White to off-white solid, suitable for laboratory use.
- High assay purity (≈99.06%).
- Acts as a reducing agent in chemical and biochemical applications.
- Soluble in water at ambient temperature.
- Available in multiple pack sizes for research and scale-up.
Medchemexpress LLC FFN270 hydrochloride | 2341841-05-0 | 99.0% | 259.66 g/mol | C11H11ClFNO3 | 5 MG
FFN270 hydrochloride is a fluorescent tracer of norepinephrine used as a fluorescent substrate for norepinephrine transporters (NET) and vesicular monoamine transporters (VMAT). Provided as the hydrochloride salt, it is intended for biochemical and cellular assays to monitor norepinephrine uptake and vesicular transport.
- Fluorescent tracer for norepinephrine transport studies.
- Acts as a substrate for NET and VMAT, enabling uptake and vesicular labeling.
- High purity (≥99.0%) suitable for research applications.
- White to off-white solid with molecular weight 259.66 g/mol and formula C11H11ClFNO3.
- Storage recommendations: sealed, protected from moisture; in solvent -80°C (6 months), -20°C (1 month).
- Available in small laboratory quantities for assay development and validation.
Medchemexpress LLC CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 g/mol | C26H30ClN5O2S | 50 MG
CGP71683 hydrochloride is a selective, non-peptide neuropeptide Y (NPY) Y5 receptor antagonist used for in vitro pharmacology and receptor signaling studies. The compound is supplied as a white solid and as a 10 mM solution in DMSO and is reported with high purity for research applications.
- Selective NPY Y5 receptor antagonist with low nanomolar affinity.
- Reported high purity suitable for research use.
- Available as a solid and as a 10 mM solution in DMSO for assay convenience.
- Molecular weight 512.07 g/mol aiding stoichiometric calculations.
- CAS registry number 192322-50-2 for unambiguous identification.
- Intended for biochemical and pharmacological studies in vitro.
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
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 5mg 564356414 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 5mg 564356414 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC CGP71683 hydrochloride | 192322-50-2 | MFCD07783999 | 99.4% | 512.07 | C26H30ClN5O2S | 10 MG
CGP71683 hydrochloride is the hydrochloride salt of a selective neuropeptide Y Y5 receptor antagonist used as a research tool in neuroscience and endocrinology. It is supplied as a high-purity solid for non-clinical laboratory use, with supporting datasheet and certificate of analysis available.
- Selective antagonist for the neuropeptide Y Y5 receptor (Ki ~1.3 nM).
- High reported purity, 99.4%.
- Molecular weight 512.07 g/mol; chemical formula C26H30ClN5O2S.
- CAS number 192322-50-2 for unambiguous identification.
- Solid powder suitable for dissolution in appropriate solvents for assays.
- Supplied with datasheet and certificate of analysis for quality assurance.
- Available in small milligram pack sizes for screening and mechanistic studies.
Medchemexpress LLC SKI-I 10mg | 306301-68-8 | 406.44 | C25H18N4O2 | 10 MG
SKI-I is a small-molecule sphingosine kinase inhibitor supplied as a 10 mg research-grade solid for laboratory use. It inhibits human sphingosine kinase with reported IC50 ≈ 1.2 μM and shows additional activity against hERK2; reported purity and storage conditions support reproducible experimental use.
- High reported purity (99.14%).
- Off-white to light yellow solid; convenient 10 mg quantity for assay development.
- Soluble in DMSO at 100 mg/mL; suitable for in vitro use and formulatable for in vivo studies.
- Storage: powder at 4°C protected from light; aliquots in solvent stable at -80°C for up to 6 months.
- Demonstrated cytotoxicity against multiple human cancer cell lines at low micromolar concentrations.