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Filtered Search Results
Medchemexpress LLC 3-(3,5-dimethylisoxazol-4-yl)-5-(hydroxy(pyridin-3-yl)methyl)phenol | 2231747-03-6 | MFCD32174354 | 99.0% | 296.32 g·mol⁻¹ | C17H16N2O3 | 5 MG
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A small-molecule research compound that acts as a potent and selective BRD4 (BET family) inhibitor, with reported cellular activity (IC50 ≈166 nM) and demonstrated antiproliferative effects in cancer cell assays. Supplied as a high-purity solid for biochemical and cellular research applications.
- Potent BRD4 inhibitor with reported IC50 ≈166 nM.
- Demonstrated antiproliferative activity in cancer cell assays.
- Molecular formula C17H16N2O3; molecular weight 296.32 g·mol⁻¹.
- High purity (98.99%).
- Supplied as a powder suitable for biochemical and cellular studies.
- Recommended storage: powder -20°C (long term) or 4°C (short term); in solvent -80°C.
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Medchemexpress LLC 2-((4,4-dimethyl-2-methylenecyclopent-1-en-1-yl)amino)-4-phenyl-1,3-naphthyridine | 511514-03-7 | ≥98.0% | 343.42 g/mol | C21H21N5 | 5 MG
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A small-molecule inhibitor that selectively binds the heterotrimeric Gαi subunit and blocks α2-adrenergic receptor-mediated regulation of intracellular cAMP. Intended for laboratory research use only.
- Selective inhibition of the Gαi subunit, blocking α2AR-mediated cAMP regulation.
- Small molecule with molecular formula C21H21N5 and molecular weight 343.42 g/mol.
- High purity (≥98%) and light yellow to yellow solid appearance.
- Soluble in DMSO (250 mg/mL); example in vivo formulations documented.
- Stable as powder at -20°C for long-term storage; defined solvent stability at lower temperatures.
- Supplied in a 5 mg quantity for laboratory testing.
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Apexbio Technology LLC EMRICASAN 5MG
EMRICASAN 5MG APEXBIO TECHNOLOGIES
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eMolecules 1253186-56-9 | Medchem Express | GSK-7975A | 5mg | 446261415 | HY-12507 | MFCD28411366 | 397.305 | C18H12F5N3O2
Medchem Express | N-563 | 5mg | 446256051 | HY-100751 | 140686-92-6 | MFCD00909426 | 359.427 | C15H29N5O5
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Medchemexpress LLC Rac-mem 1003 | 165187-25-7 | 99.6% | 100 MG
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(Rac)-MEM 1003 is the racemate of MEM 1003, a dihydropyridine compound that antagonizes L-type Ca2+ channels and is used in preclinical research into neurodegenerative disorders such as Alzheimer's disease. The compound is supplied as a solid powder with chemical formula C22H25ClN2O5 and a molecular weight of 432.90 g/mol.
- Racemic dihydropyridine L-type calcium channel antagonist.
- High purity solid suitable for research (99.6%).
- Molecular formula C22H25ClN2O5; molecular weight 432.90 g/mol.
- Available in small research quantities, including 100 MG solid packages.
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Medchemexpress LLC Imirestat | 89391-50-4 | 99.6% | 286.24 | 100 MG
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Imirestat (AL 1576) is an aldose reductase inhibitor used for the treatment of diabetes. For research use only, MedChemExpress does not sell to patients.
- Aldose reductase inhibitor
- Used for the treatment of diabetes
- Purity: 99.59%
- Improves nerve conduction velocity
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Medchemexpress LLC Cobimetinib racemate | 934662-91-6 | 99.4% | 531.31 g/mol | C21H21F3IN3O2 | 5 MG
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Cobimetinib racemate is the racemic analytical standard of Cobimetinib, a potent and selective MEK inhibitor used in research to probe MAPK/ERK signaling and MEK-dependent cellular responses. Supplied as a high-purity solid for analytical and laboratory applications, it is intended for use in assay development, compound characterization, and mechanistic studies.
- Racemic analytical standard for Cobimetinib
- Potent and selective MEK inhibitor for MAPK/ERK pathway studies
- High purity (~99.4%) suitable for analytical applications
- Available in small mg quantities for research use
- Solid, white to light yellow appearance
- Molecular weight 531.31 g/mol; formula C21H21F3IN3O2
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eMolecules 27361-16-6 | 2-butoxypyridine | Combi-Blocks, Inc. | MFCD00006267 | 151.209 | C9H13NO | 97.000 | CCCCOc1ccccn1 | 25g | 603135992
2-butoxypyridine | Combi-Blocks, Inc. | 27361-16-6 | MFCD00006267 | 151.209 | C9H13NO | 97.000 | CCCCOc1ccccn1 | 25g | 603135992
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eMolecules 90357-05-4 | Desfluoro bicalutamide | Combi-Blocks | MFCD24386587 | 412.380 | C18H15F3N2O4S | 95.000 | CC(O)(CS(=O)(=O)c1ccccc1)C(=O)Nc1ccc(C#N)c(c1)C(F)(F)F | 1g | 415502187
Desfluoro bicalutamide | Combi-Blocks | 90357-05-4 | MFCD24386587 | 412.380 | C18H15F3N2O4S | 95.000 | CC(O)(CS(=O)(=O)c1ccccc1)C(=O)Nc1ccc(C#N)c(c1)C(F)(F)F | 1g | 415502187
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eMolecules 442898-34-2 | Medchem Express | NCGC00092410 | 5mg | 572596557 | HY-114043 | 353.466 | C21H27N3O2
Medchem Express | ML365 | 5mg | 446261098 | HY-12345 | 947914-18-3 | MFCD09204310 | 360.413 | C22H20N2O3
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Medchemexpress LLC Imifoplatin (PT-112) | 1339960-28-9 | 95.0% | 485.23 g·mol⁻¹ | C6H16N2O7P2Pt | 5 MG
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Imifoplatin is a platinum-containing phosphaplatin research compound with reported antitumor activity and the ability to induce apoptosis and immunogenic cell death. It is provided as a high-purity reagent in a small research-scale quantity and is intended for preclinical and in vitro studies. Documentation such as the safety data sheet and certificate of analysis is available with the product.
- Platinum-containing phosphaplatin class compound.
- Exhibits antitumor activity and can induce apoptosis.
- Causes immunogenic cell death in experimental models.
- High purity: 95.0%.
- Molecular weight 485.23 g·mol⁻¹; formula C6H16N2O7P2Pt.
- Supplied in small, research-scale quantity suitable for preclinical use.
- Includes safety and quality documentation (SDS, COA).
- For research use only; not for human or veterinary use.
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Medchemexpress LLC HY-B0745 100mg , Ramatroban BAY u3405 CAS:116649-85-5 Purity:98%
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Medchemexpress, HY-B0745 100mg Ramatroban BAY u3405 CAS:116649-85-5 Formula:C21H21FN2O4S IC50: 14 nM (hTP, TxA 2 ), 113 nM (hDP2, CRTH2), 33.4 μM (hDP1), 15 μM (CYP2C9) Purity:98% Ramatroban is a selective thromboxane A 2 ( TxA 2 , IC 50 =14 nM) antagonist, which also antagonizes CRTH2 ( IC 50 =113 nM) by inhibiting PGD 2 binding. 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 HY-18966 5mg Medchemexpress, PF-04418948 CAS:1078166-57-0 Purity:>98%
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Medchemexpress, HY-18966 5mg PF-04418948 CAS:1078166-57-0 PF-04418948 is an orally active, potent and selective prostaglandin EP2 receptor antagonist with an IC50 of 16 nM. 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 HY-18990 2mg Medchemexpress, GSK180736A CAS:817194-38-0 Purity:>98%
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Medchemexpress, HY-18990 2mg GSK180736A CAS:817194-38-0 GSK180736A is potent Rho-associated coiled-coil kinase 1 (ROCK1) inhibitor with an IC50 of 100 nM. GSK180736A is also a selective and ATP-competitive G protein-coupled receptor kinase 2 (GRK2) inhibitor with an IC50 of 0.77 μM. 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 GLP-1R antagonist 1 (compound 5d) | 488097-06-9 | 99.7% | 440.73 g/mol | C16H11ClF6N4O2 | 100 MG
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GLP-1R Antagonist 1 (compound 5d) is a small-molecule, non-competitive antagonist of the glucagon-like peptide-1 receptor (GLP-1R). It is reported to be orally active and CNS-penetrant, with an IC50 of approximately 650 nM, and is supplied as a powder for research use.
- Orally active and CNS penetrant.
- Non-competitive GLP-1R antagonist with reported IC50 ≈ 650 nM.
- Provided as a powder suitable for in vitro and in vivo studies.
- Molecular weight 440.73 g/mol; formula C16H11ClF6N4O2.
- Recommended storage: powder at -20°C; solutions at -80°C for long-term stability.
- High reported purity (approximately 99.7%).
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