Aminophenols
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.
Medchemexpress LLC SKI-I | 5MG
SKI-I is a potent and selective inhibitor of human sphingosine kinase (SK) with an IC50 of 1 2 M for ST-hSK SKI-I also inhibits hERK2 (IC50 11 M) SKI-I induces apoptosis in tumor cell lines[1][2]
eMolecules Key Organics/BIONET Medetomidine Hydrochloride 6mg 564356415 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 6mg 564356415 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC PZ703b hydrochloride | 99.2% | 1636.90 g/mol | C80H103Cl2F3N10O11S4 | 5 MG
PZ703b hydrochloride is a Bcl-xL-targeting PROTAC degrader that induces apoptosis and inhibits cancer cell proliferation. Supplied as a high-purity hydrochloride salt in small-quantity research packs, it is intended for in vitro studies such as bladder cancer research.
- Targets Bcl-xL to promote proteasomal degradation and trigger apoptosis.
- High purity (≈99.2%) suitable for biological assays.
- Available in small pack sizes for early-stage research.
- Provided as a hydrochloride salt to aid solubility and handling.
- Relevant for studies of cancer cell proliferation and bladder cancer models.
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 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 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 LY294002 hydrochloride | 934389-88-5 | MFCD01530034 | 99.9% | 343.8 g/mol | C19H18ClNO3 | 10 MG
LY294002 hydrochloride is a research-grade small-molecule inhibitor of phosphoinositide 3-kinase (PI3K) and casein kinase 2 (CK2) used to investigate PI3K/AKT signaling, apoptosis, and autophagy in cell biology and cancer research. Provided as a solid reagent with high chemical purity for in vitro and biochemical studies; not for human or veterinary use.
- Inhibits PI3K and CK2 kinase activity for pathway interrogation.
- Supports studies of apoptosis, autophagy, and cell signaling.
- High purity (99.93%) suitable for biochemical and cell-based assays.
- Available in small solid quantities for laboratory workflows.
- Standard chemical identifiers (CAS, MFCD) provided for reference.
eMolecules Ambeed / 3-Bromo-2-hydroxybenzoic acid / 250mg / 490557462 / A362033 / / 3883-95-2 / MFCD03265705 / 217.018 / C7H5BrO3
Ambeed / 3-Bromo-2-hydroxybenzoic acid / 250mg / 490557462 / A362033 / / 3883-95-2 / MFCD03265705 / 217.018 / C7H5BrO3
Medchemexpress LLC Irigenin | 548-76-5 | MFCD00597047 | 99.8% | 360.31 g/mol | C18H16O8 | 10 MG
Irigenin is an isoflavone research compound used to inhibit Extra Domain A (EDA)-integrin interactions and to study integrin-mediated signaling and apoptosis in vitro. It is supplied as a solid powder and as DMSO solutions for assay preparation.
- Inhibits EDA-integrin interactions and is used in integrin and apoptosis research.
- High purity (99.84%) suitable for research applications.
- Molecular weight 360.31 g/mol; chemical formula C18H16O8.
- CAS number 548-76-5 for unambiguous identification.
- Available as solid powder and 10 mM solutions in DMSO for assay use.
- Available in small research pack sizes including 10 MG.