Aminophenols
Medchemexpress LLC Bestatin-d7 (hydrochloride) | 97.7% | 1 MG
Bestatin-d7 (hydrochloride) is a deuterium-labeled version of Bestatin (hydrochloride). Bestatin hydrochloride is an inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase, primarily utilized in cancer research.
- Deuterium labeled compound
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Inhibitor of CD13 (Aminopeptidase N)/APN and leukotriene A4 hydrolase
Medchemexpress LLC Prilocaine-d7 hydrochloride | 98.2% | 500 UG
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
Medchemexpress LLC MK-0493 (hydrochloride) | 455957-71-8 | 98.8% | 582.55 | C30H39Cl2F2N3O2 | 1 ML
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.
Medchemexpress LLC Pirmenol hydrochloride | 61477-94-9 | MFCD01691662 | 98.8% | 374.95 g·mol⁻¹ | C22H31ClN2O | 100 MG
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.
Medchemexpress LLC SAR7334 hydrochloride | 1333207-63-8 | 98.0% | 440.79 g/mol | C21H24Cl3N3O | 10 MG
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.
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
Medchemexpress LLC HY-117288A 5mg Medchemexpress, S55746 (hydrochloride) CAS:1448525-91-4 Purity:>98%
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.
Medchemexpress LLC Ly266097 hydrochloride | 172895-39-5 | MFCD00949080 | >98.0% | 407.33 g·mol⁻¹ | C21H23ClN2O2 · HCl | 25 MG
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.
Medchemexpress LLC Hypidone hydrochloride | 1339058-04-6 | 99.7% | 334.84 g/mol | C18H23ClN2O2 | 10 MG
Hypidone hydrochloride is the hydrochloride salt of a research compound reported to modulate 5-HT receptors and inhibit serotonin uptake in preclinical studies. It is supplied as a high-purity solid for laboratory use, typically in milligram-scale vials for in vitro and in vivo research.
- High reported purity (>99%).
- Molecular weight 334.84 g/mol.
- Solid hydrochloride salt, white to off-white powder.
- Reported activity as a 5-HT receptor modulator and uptake inhibitor in preclinical models.
- Packaged in small, milligram-scale quantities suitable for research.
Cayman Chemical Acetaminophen Inhibitors
An analgesic and antipyretic compound; an inhibitor of COX-2 that is selective over COX-1 (IC50s = 113.7 and 25.8 µM, respectively, in human blood ex vivo); induces ferroptotic cell death in primary mouse hepatocytes; has a metabolite that depletes glutathione reserves in the liver
Medchemexpress LLC NPS-2143 hydrochloride | 324523-20-8 | MFCD16038896; MFCD04113010 | 100.0% | 445.38 g/mol | C24H26Cl2N2O2 | 50 MG
NPS-2143 hydrochloride is an orally active calcilytic small molecule that selectively antagonizes the calcium-sensing receptor (CaSR), inhibiting CaSR-mediated increases in intracellular Ca2+. It is supplied as a solid at high purity for use in biochemical and pharmacological research into CaSR signaling and related physiological pathways.
- Selective CaSR antagonist for CaSR signaling studies.
- Orally active calcilytic small molecule suitable for in vitro and in vivo research.
- High purity solid appropriate for research applications.
- Molecular weight 445.38 g/mol and chemical formula C24H26Cl2N2O2.
- Available in small research quantities, including 50 MG.
- Applicable to biochemical, cellular, and pharmacological assays.
eMolecules 2,4-Diaminophenol sulfate | 74283-34-4 | MFCD01321156 | 1g
Combi-Blocks, Inc. | 2,4-Diaminophenol sulfate | 1g | 603144863 | QC-1959 | 98.000 | 74283-34-4 | MFCD01321156 | 222.220 | C6H10N2O5S
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Medchemexpress LLC Acetaminophen glucuronide-d3 sodium salt | 1260619-61-1 | 97.8% | 352.29 g/mol | C14H13D3NNaO8 | 2.5 MG
Acetaminophen glucuronide-d3 sodium salt is the deuterium-labeled sodium salt of acetaminophen glucuronide, supplied as a stable isotope standard for analytical and metabolic research. It is intended as a reference material for quantitative mass spectrometry and chromatographic assays to improve accuracy and traceability in metabolite measurement.
- Deuterium-labeled sodium salt suitable as an internal standard.
- Enables accurate MS and LC quantitation of acetaminophen metabolites.
- Molecular formula C14H13D3NNaO8; molecular weight 352.29 g/mol.
- Provided in a research-grade, solid form for laboratory use.
- For research use only; not for human or clinical use.
Sigma Aldrich Fine Chemicals Biosciences Acetaminophen BioXtra, >=99.0% | 103-90-2 | MFCD00002328 | 1KG
Acetaminophen BioXtra, >=99.0% | Purity: >=99.0% | Mol Wt: 151.16 | 103-90-2 | MFCD00002328 | 1KG
Medchemexpress LLC Va-k-14 hydrochloride | 1171341-19-7 | 99.0% | 10MM 1ML
Va-k-14 hydrochloride | 1171341-19-7 | 99.0% | 10MM 1ML