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Filtered Search Results
eMolecules 1448525-91-4 | Medchem Express | S55746 (hydrochloride) | 5mg | 482204184 | HY-117288A | 747.29 | C43H43ClN4O6
Ambeed | (S)-4-Isopropyl-2-(6-methylpyridin-2-yl)-45-dihydrooxazole | 250mg | 649269036 | A1476164 | 199277-70-8 | 204.273 | C12H16N2O
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Medchemexpress LLC Cgp55845 hydrochloride | 149184-22-5 | MFCD09266221 | 99.1% | 438.71 g/mol | C18H23Cl3NO3P | 5 MG
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CGP55845 hydrochloride is the hydrochloride salt of CGP55845, a potent and selective GABAB receptor antagonist with low-nanomolar potency (IC50 ≈ 5-6 nM). It is supplied as a solid for research use in receptor pharmacology and neurological studies.
- Potent GABAB receptor antagonist with low-nanomolar activity.
- High purity (99.1%) suitable for research applications.
- Molecular weight 438.71 g/mol, well characterized.
- CAS number 149184-22-5 for unambiguous identification.
- Provided as the hydrochloride salt in a 5 mg pack for small-scale experiments.
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Medchemexpress LLC 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-oxo-1,4-dihydroquinazoline-3-carboxylate hydrochloride | 131780-48-8 | MFCD00911718 | 99.0% | 351.83 g/mol | C17H22ClN3O3 | 5 MG
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DAU 5884 hydrochloride is a potent, selective muscarinic M3 receptor antagonist provided as the hydrochloride salt for research use. It is used in vitro to study muscarinic receptor-mediated signaling, including methacholine-dependent cell proliferation and smooth muscle contractility.
- Potent M3 receptor antagonist suitable for in vitro pharmacology.
- Inhibits methacholine-dependent cell proliferation and muscle contractility.
- High reported purity for reliable experimental results.
- Available in small milligram quantities for screening and characterization.
- Soluble in water and DMSO for diverse assay formats.
- Provided as a hydrochloride salt for improved stability and handling.
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Medchemexpress LLC N-[1-(3,4-dimethoxyphenyl)ethylideneamino]-3-(4-methoxyphenyl)-1H-pyrazole-5-carboxamide | 1259484-97-3 | 99.3% | 394.42 g/mol | C21H22N4O4 | 5 MG
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SKI-178 is a small-molecule inhibitor of sphingosine kinase 1 (SphK1) and sphingosine kinase 2 (SphK2) that induces apoptosis in various cancer cell lines. It is provided as a high-purity research reagent for in vitro studies, with reported cytotoxic activity in the low micromolar range.
- Potent SphK1 and SphK2 inhibition
- Cytotoxic in cancer cell lines at low micromolar concentrations
- High purity suitable for research applications
- Available in multiple package sizes for screening and follow-up studies
- Molecular weight 394.42 and formula C21H22N4O4
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Medchemexpress LLC SKI-I | 5MG
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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]
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Aobchem 2 4-Dibromo-3-fluoro-1 5-dimethylbenzene | 95% | C8H7Br2F | 500mg
2 4-Dibromo-3-fluoro-1 5-dimethylbenzene | 95% | C8H7Br2F | 500mg
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eMolecules SODIUM METHANESULFINATE 1000G
5000189193 SODIUM METHANESULFINATE 1000G
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Aobchem 2 4-Di-tert-amylphenol | 95% | CAS 120-95-6 | C16H26O | 1kg
2 4-Di-tert-amylphenol | 95% | CAS 120-95-6 | C16H26O | 1kg
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Aobchem Tetrahydro-4-(8-hydroxy-1 4-dioxaspiro[4 5]dec-8-yl)-2H-pyran-4-carbonitrile | 95% | CAS 1521009-01-7 | C14H21NO4 | 5g
Tetrahydro-4-(8-hydroxy-1 4-dioxaspiro[4 5]dec-8-yl)-2H-pyran-4-carbonitrile | 95% | CAS 1521009-01-7 | C14H21NO4 | 5g
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Medchemexpress LLC 4-(dimethylamino)pyridine | 1122-58-3 | MFCD00006418 | 122.17 g/mol | C7H10N2 | 1000g
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4-Dimethylaminopyridine is an acyl transfer catalyst 4-Dimethylaminopyridine is used for labeling and analysis of glycoproteins on the surface of living cells 4-Dimethylaminopyridine reduces dyskinesia attacks[1][2]
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Ambeed 1Bromo2iodobenzene
1-Bromo-2-iodobenzene, 583-55-1, 98% (stabilized with Copper chip)
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Ambeed 1 1 Biphenyl 4carboxylic acid
[1,1'-Biphenyl]-4-carboxylic acid, 92-92-2, 98%
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Medchemexpress LLC Acetaminophen-d7 | 1219798-53-4 | 99.9% | C8H2D7NO2 | 1 MG
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Acetaminophen-d7 is the deuterium labeled Acetaminophen. Acetaminophen (Paracetamol) is a selective cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 25.8 μM; it is a widely used antipyretic and analgesic agent and a potent hepatic N-acetyltransferase 2 (NAT2) inhibitor.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
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Medchemexpress LLC HY-100689 5mg Medchemexpress, Propyl pyrazole triol CAS:263717-53-9 Purity:>98%
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Medchemexpress, HY-100689 5mg Propyl pyrazole triol CAS:263717-53-9 Propyl pyrazole triol (PPT) is an estrogen receptor alpha (ERα) agonist. The relative binding affinity of Propyl pyrazole triol for ERα (ERα: 49%) around 410 times higher compared with estrogen receptor beta (ERβ: 0.12%) [1] . 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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Ambeed AMBEED
5000847572 TRIMANGANESE TETRAOXIDE 1000G
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