Aminophenols
Medchemexpress LLC Ly294002 (hydrochloride) | 934389-88-5 | MFCD00270881 | 99.9% | 343.80 g/mol | C19H18ClNO3 | 100 MG
LY294002 hydrochloride is the hydrochloride salt of LY294002, a broad-spectrum phosphoinositide 3-kinase (PI3K) inhibitor that also shows activity against CK2 and DNA-PK. Supplied for research use in powder and solution formats, it is used to probe PI3K signaling, apoptosis, and related kinase pathways. CAS 934389-88-5; molecular weight 343.80 g/mol; high purity suitable for biochemical and cell-based assays.
- Potent PI3K inhibitor useful for signaling studies.
- Also inhibits CK2 and DNA-PK, enabling broader kinase pathway interrogation.
- Available as powder and as DMSO solution for flexible dosing.
- High purity suitable for biochemical and cell-based assays.
- Stable when stored sealed at 4°C, away from moisture.
- Widely used in oncology and cell signaling research applications.
Medchemexpress LLC LY294002 (hydrochloride) | 934389-88-5 | MFCD01530034 | 99.9% | 343.8 g/mol | C19H18ClNO3 | 25 MG
LY294002 (hydrochloride) is a research-grade small-molecule inhibitor of phosphoinositide 3-kinases (PI3K) and casein kinase 2 (CK2), used to probe PI3K-mediated signaling, apoptosis, and autophagy in cellular and in vivo studies. It is supplied as a high-purity solid for laboratory research.
- Potent inhibitor of PI3K and CK2.
- High declared purity (>99.9%).
- Supplied as a solid for laboratory use.
- Molecular formula C19H18ClNO3; molecular weight 343.8 g/mol.
- Available in small research quantities such as 25 MG.
- Comes with an SDS and technical documentation for safe handling.
Medchemexpress LLC RS 67333 hydrochloride | 168986-60-5 | MFCD00938576 | 99.7% | 389.36 g/mol | C19H30Cl2N2O2 | 1 ML
RS 67333 hydrochloride is a research reagent that functions as a potent, selective partial agonist of the 5-HT4 (serotonin 4) receptor. It is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) and in multiple solid pack sizes for use in pharmacology and neuroscience studies, including neuroprotection and Alzheimer's disease research. CAS: 168986-60-5; purity ~99.7%.
- Potent, selective 5-HT4 receptor partial agonist.
- Offered as 10 mM solution in DMSO (1 mL) and multiple solid sizes.
- High listed purity (~99.7%).
- Suitable for pharmacology and neuroscience research applications.
- Provided with datasheet, certificate of analysis, and safety data sheet.
TARGETMOL CHEMICALS INC E7016 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. E7016 (GPI 21016) is an orally available PARP inhibitor. E7016 inhibits of DNA repair. E7016 can enhance tumor cell radiosensitivity in vitro and in vivo. purity: 98%
eMolecules Key Organics/BIONET - Building Blocks Medetomidine Hydrochloride 4mg 344516857 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET - Building Blocks Medetomidine Hydrochloride 4mg 344516857 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Medchemexpress LLC Metixene hydrochloride hydrate | 7081-40-5 | 99.9% | 1 ML
Metixene hydrochloride hydrate is supplied as a 10 mM solution in DMSO for research use. It is the hydrochloride salt of metixene, an anticholinergic and antiparkinsonian agent, provided in a 1 mL vial.
- Ready-to-use 10 mM solution in DMSO.
- Compact 1 mL vial for small-scale assays.
- High purity suitable for research applications.
- Molecular formula C20H26ClNOS, molecular weight 363.94 g/mol.
- Suitable for in vitro pharmacology and receptor studies.
Medchemexpress LLC Rs 17053 hydrochloride | 169505-93-5 | 99.9% | 449.41 g/mol | C24H30Cl2N2O2 | 10 MG
RS 17053 hydrochloride is a potent, selective α1A adrenoceptor antagonist for pharmacological research. It exhibits high affinity in native membranes (pKi 9.1) and functional potency (pA2 9.8), with marked selectivity versus α1B and α1D subtypes. The material is supplied as a high-purity solid and is provided in multiple sizes and a DMSO solution format for laboratory use.
- Potent, selective α1A adrenoceptor antagonist with reported pKi 9.1 and pA2 9.8.
- Substantial selectivity versus α1B and α1D receptor subtypes.
- High purity suitable for sensitive pharmacology assays.
- Available as a solid and as a ready-to-use DMSO solution for convenience.
- Intended for research use in receptor binding and functional studies.
eMolecules Ambeed / 5-Methyl-2-nitrophenol / 5g / 525111679 / A194739 / / 700-38-9 / MFCD00007111 / 153.137 / C7H7NO3
Ambeed / 5-Methyl-2-nitrophenol / 5g / 525111679 / A194739 / / 700-38-9 / MFCD00007111 / 153.137 / C7H7NO3
Medchemexpress LLC Bepridil hydrochloride | 68099-86-5 | MFCD00065498 | 100.0% | 403.0 g/mol | C24H35ClN2O | 1 ML
Bepridil hydrochloride is the hydrochloride salt of bepridil, a non-selective calcium channel blocker used in research to probe cardiac ion channels and antianginal mechanisms. Supplied for research and analytical applications, it is available as a solid and as a prepared solution.
- Non-selective calcium channel blocker used in electrophysiology and pharmacology studies.
- Hydrochloride salt form enhances solubility for assays.
- Available as solid and as a 10 mM solution in DMSO for ready-to-use experiments.
- High purity (~99.98%) appropriate for analytical standards.
- Well-characterized identifiers: CAS 68099-86-5; molecular weight 403.0 g/mol.
Medchemexpress LLC RS100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 5 MG
RS100329 hydrochloride is a selective α1A-adrenoceptor antagonist for research use that inhibits reflex urethral contractions and is used in studies of benign prostatic hyperplasia. The compound is supplied as the hydrochloride salt with high analytical purity and characterized molecular properties.
- CAS number 1215654-26-4.
- Molecular formula C20H26ClF3N4O3.
- Molecular weight 462.89 g/mol.
- Purity 99.6%.
- Solubility in DMSO 31.25 mg/mL (67.51 mM); ultrasonic assistance recommended.
- Recommended storage solid at 4°C, protect from light; in solvent -80°C for up to 6 months, -20°C for up to 1 month.
- Intended for research use only; not for human or veterinary use.
Medchemexpress LLC Rs100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 10 MG
RS100329 hydrochloride is a selective α1A-adrenoceptor antagonist supplied as the hydrochloride salt for research use. It is reported to have high affinity for α1A (pKi ≈ 9.6) with lower affinity for α1D and α1B, and is used in preclinical studies including investigations of urethral reflex contractions and benign prostatic hyperplasia.
- Selective α1A-adrenoceptor antagonist for receptor pharmacology research.
- High reported purity suitable for preclinical assays.
- Supplied as a stable hydrochloride salt in solid form.
- Available in small milligram pack sizes for early-stage studies.
Medchemexpress LLC RS100329 hydrochloride | 1215654-26-4 | 99.6% | 462.89 g/mol | C20H26ClF3N4O3 | 100 MG
RS100329 hydrochloride is the hydrochloride salt of a potent and subtype-selective α1A-adrenoceptor antagonist used as a research reagent in receptor pharmacology and selectivity studies. The compound is supplied as a solid, with a reported molecular weight of 462.89 g/mol and high batch-specific purity; consult the certificate of analysis for exact values and handling instructions.
- Potent, selective α1A-adrenoceptor antagonist.
- Hydrochloride salt form for improved stability and handling.
- High purity suitable for in vitro pharmacology (COA available).
- Supplied as a solid for dissolution in common organic solvents.
- Used in receptor binding and functional assays to assess selectivity.