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Filtered Search Results
Medchemexpress LLC Prilocaine-d7 hydrochloride | 98.2% | 500 UG
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Prilocaine-d7 hydrochloride is a deuterium-labeled form of Prilocaine hydrochloride, an amino amide and a Na, K-ATPase inhibitor. Known to have neurotoxic effects, this compound is for research use only and not sold to patients. Its deuterated nature can impact pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis via NMR, GC-MS, or LC-MS
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Medchemexpress LLC MK-0493 (hydrochloride) | 455957-71-8 | 98.8% | 582.55 | C30H39Cl2F2N3O2 | 1 ML
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MK-0493 hydrochloride is a potent, orally active, and selective agonist of the melanocortin receptor 4 (MC4R), provided as a 10 mM solution in DMSO (1 mL) for preclinical research. The compound is characterized with confirmed purity and molecular data to support reproducible metabolic and neuronal signaling studies.
- Potent and selective MC4R agonist for metabolic research.
- Ready-to-use 10 mM solution in DMSO (1 mL) for immediate experiments.
- High purity suitable for preclinical work.
- Characterized molecular weight and formula provided for reproducibility.
- Also available as solid quantities for dosing flexibility.
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Medchemexpress LLC Pirmenol hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g·mol⁻¹ | C22H31ClN2O | 100 MG
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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.
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Medchemexpress LLC SAR7334 hydrochloride | 1333207-63-8 | 98.0% | 440.79 g/mol | C21H24Cl3N3O | 10 MG
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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.
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eMolecules Medchem Express / Propyl pyrazole triol / 5mg / 475641433 / HY-100689 / / 263717-53-9 / MFCD03453628 / 386.451 / C24H22N2O3
Medchem Express / Propyl pyrazole triol / 5mg / 475641433 / HY-100689 / / 263717-53-9 / MFCD03453628 / 386.451 / C24H22N2O3
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Medchemexpress LLC PZ703b hydrochloride | 99.2% | 1636.90 g/mol | C80H103Cl2F3N10O11S4 | 5 MG
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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.
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eMolecules Key Organics/BIONET Medetomidine Hydrochloride 20mg 564356420 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
Key Organics/BIONET Medetomidine Hydrochloride 20mg 564356420 AS-2748 99 000 86347-15-1 236 740 C13H17ClN2
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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
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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
Medchem Express / S55746 / 5mg / 446260465 / HY-117288 / / 1448584-12-0 / [null] / 710.831 / C43H42N4O6
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Medchemexpress LLC HY-117288A 5mg Medchemexpress, S55746 (hydrochloride) CAS:1448525-91-4 Purity:>98%
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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.
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Medchemexpress LLC Ly266097 hydrochloride | 172895-39-5 | MFCD00949080 | >98.0% | 407.33 g·mol⁻¹ | C21H23ClN2O2 · HCl | 25 MG
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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.
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Medchemexpress LLC Guvacine hydrochloride | 6027-91-4 | 99.9% | 163.60 g·mol⁻¹ | C6H10ClNO2 | 100 MG
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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.
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Medchemexpress LLC ZM39923 hydrochloride | 1021868-92-7 | MFCD04974534 | 99.8% | 367.91 g/mol | C23H26ClNO | 5MG
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ZM39923 hydrochloride is a research-grade small molecule that acts primarily as a JAK3 inhibitor (pIC50 = 7.1) and also potently inhibits tissue transglutaminase (TGM2) (IC50 ≈ 10 nM). It displays weaker activity against EGFR and JAK1 and minimal activity versus Lck and CDK4. Supplied as the hydrochloride salt with high reported purity, it is intended for laboratory research use only.
- JAK3 inhibitor with pIC50 7.1.
- Potent tissue transglutaminase (TGM2) inhibition (IC50 ≈ 10 nM).
- Hydrochloride salt form for improved stability and handling.
- High reported purity (around 99.8%).
- Available as solid and as a DMSO solution format.
- Intended for research use only; not for diagnostic or therapeutic use.
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Medchemexpress LLC Ozanimod hydrochloride | 1618636-37-5 | 98.1% | 5 MG
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Ozanimod hydrochloride is the hydrochloride salt of ozanimod, a selective sphingosine 1-phosphate (S1P) receptor modulator used in research on immune-mediated disorders such as relapsing multiple sclerosis. It is supplied as a white to off-white solid with high purity for in vitro and in vivo pharmacology studies.
- High purity (98.1%).
- Molecular weight 440.92 g/mol; formula C23H25ClN4O3.
- Soluble in DMSO at ≥ 200 mg/mL for stock solutions.
- Suitable for in vitro and in vivo pharmacology applications.
- Supplied as a 5 MG quantity.
- Store sealed at 4°C; in solvent store -80°C for up to 6 months or -20°C for 1 month.
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