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Filtered Search Results
Ambeed AMBEED
5000886513 8-AMINOQUINOLINE 25G
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Medchemexpress LLC Ro 31-9790 | 145337-55-9 | 99.4% | 315.41 g/mol | C15H29N3O4 | 1 ML
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Ro 31-9790 is a synthetic metalloproteinase (MMP) inhibitor used in biochemical and cell-based research. It blocks L-selectin shedding and modulates cytokine shedding in immune cells, displaying submicromolar to micromolar potency across different cell types. The compound is provided as a concentrated solution for laboratory assays and requires appropriate storage and handling.
- Inhibits L-selectin and TNF-α shedding in immune cells.
- Potent activity with IC50 values as low as 0.3 μM.
- Supplied as a 10 mM solution in DMSO for ready-to-use dosing.
- High purity suitable for research applications.
- High DMSO solubility (50 mg/mL) with warming or sonication if needed.
- Stable in solvent when stored at -80°C for long-term preservation.
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Medchemexpress LLC (2R)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N'-hydroxy-2-(2-methylpropyl)butamid | 145337-55-9 | 99.4% | 315.41 g/mol | C15H29N3O4 | 100 MG
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Ro 31-9790 is a synthetic matrix metalloproteinase (MMP) inhibitor provided for research use. It serves as a biochemical probe to study MMP-related activity in vitro and in cell-based assays. The compound is identified by CAS 145337-55-9 and is characterized by a defined molecular formula and high reported purity.
- Acts as a matrix metalloproteinase inhibitor for research applications.
- High purity, approximately 99.4%.
- Molecular weight 315.41 g/mol; formula C15H29N3O4.
- Suitable as a research-grade chemical for biochemical and cell biology studies.
- Synonyms and systematic names are available in chemical databases for cross-referencing.
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Apexbio Technology LLC Tempo 2564-83-2 200mg
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Tempo (CAS 2564-83-2) is a stable nitroxide radical widely employed in biomedical research for its redox-active properties It facilitates the dismutation of superoxide radicals thereby modulating mitochondrial reactive oxygen species (ROS) levels and influencing cellular oxidative stress responses Tempo also serves as an oxidation catalyst particularly in the transformation of primary alcohols to aldehydes Studies indicate that Tempo exerts both antioxidant and mutagenic effects inducing DNA strand breaks and displaying cytotoxic and mutagenic activities in in vitro models such as murine lymphoma cells It is utilized for investigating oxidative stress redox regulation and chemical mutagenesis
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eMolecules 1352796-65-6 | 2-FLUORO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIMIDINE | AstaTech | MFCD13182191 | 224.040 | C10H14BFN2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cnc(F)nc1 | 1g | 587336250
2-FLUORO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIMIDINE | AstaTech | 1352796-65-6 | MFCD13182191 | 224.040 | C10H14BFN2O2 | 95.000 | CC1(C)OB(OC1(C)C)c1cnc(F)nc1 | 1g | 587336250
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Medchemexpress LLC Daclatasvir | 1009119-64-5 | MFCD18074519 | 98.7% | 738.88 g/mol | C40H50N8O6 | 200 MG
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Daclatasvir is a potent NS5A inhibitor used as a research reagent to study hepatitis C virus replication and related pharmacology. The compound shows picomolar-range antiviral activity across multiple HCV genotypes and also inhibits OATP1B and OATP1B3 transporters. It is supplied as a high-purity solid and is commonly provided in solution formats for in vitro assays.
- Potent NS5A inhibition with EC50s in the picomolar range.
- High purity suitable for biochemical and cellular assays.
- Available in multiple pack sizes for small- and large-scale experiments.
- Soluble in DMSO and commonly supplied as 10 mM solution for convenience.
- Also inhibits OATP1B and OATP1B3, relevant for transporter studies.
- Molecular weight 738.88 g/mol for formula-based calculations.
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eMolecules 104530-79-2 | (S)-Tetrahydrofuran-3-amine | Accela ChemBio (ASD) | MFCD08234425 | 87.122 | C4H9NO | 97.000 | N[C@H]1CCOC1 | 5g | 528277004
(S)-Tetrahydrofuran-3-amine | Accela ChemBio (ASD) | 104530-79-2 | MFCD08234425 | 87.122 | C4H9NO | 97.000 | N[C@H]1CCOC1 | 5g | 528277004
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Medchemexpress LLC Fasiglifam (TAK-875) | 1000413-72-8 | MFCD18251445 | 99.0% | 524.63 | C29H32O7S | 200 MG
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Fasiglifam (TAK-875) is a potent, selective, orally bioavailable GPR40 (FFAR1) agonist used in research to study glucose-dependent insulin secretion and GPR40 pharmacology. The compound is supplied as a solid research reagent with documented potency and chemical characterization (formula C29H32O7S; MW 524.63 g/mol).
- Potent, selective GPR40 agonist with reported EC50 of 72 nM.
- Orally bioavailable pharmacology profile suitable for in vitro and in vivo studies.
- High purity (~99%) suitable for laboratory research.
- Available in multiple sizes including milligram and gram quantities.
- Chemical formula C29H32O7S and molecular weight 524.63 g/mol.
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Medchemexpress LLC B7-H2/ICOSLG Mouse 50ug
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B7-H2/ICOSLG is an important ligand of the T cell receptor ICOS and mediates immune responses It acts as a costimulatory signal promoting T and B cell proliferation cytokine secretion and plasma cell differentiation B7-H2/ICOSLG Protein Mouse (HEK293 His) is the recombinant mouse-derived B7-H2/ICOSLG protein expressed by HEK293 with C-His labeled tag
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Medchemexpress LLC Gilteritinib | 1254053-43-4 | 200MG
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Gilteritinib (ASP2215) is a potent and ATP-competitive FLT3/AXL inhibitor with IC50s of 0 29 nM/0 73 nM respectively
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382624 POMALIDOMIDE-AMIDO-C 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000665532 INFLUENZA HA 307-31 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000382670 BENZYL-PEG6-AMINE 1G
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Medchemexpress LLC ROSIGLITAZONE HYDRO | 200MG
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ROSIGLITAZONE HYDRO | 200MG
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Aobchem AOBCHEM
5000874396 ETHYL 2- 5-CYCLOBUTYL-2-FLUORO
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