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Filtered Search Results
Apexbio Technology LLC MK-571 115104-28-4 5mg
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MK-571 (CAS 115104-28-4) also known as L-660711 is a selective antagonist of the leukotriene D4 (LTD4) receptor a G protein-coupled receptor activated by cysteinyl leukotrienes involved in inflammatory responses MK-571 demonstrates high affinity for the LTD4 receptor with reported Ki values of 0 22 nM in guinea pig lung and 2 1 nM in human lung membranes It effectively antagonizes LTD4- and LTE4-induced contractions in guinea pig and human airway tissues as indicated by pA2 values ranging from 8 5 to 10 5 In vivo MK-571 reduces airway hyperresponsiveness and leukocyte infiltration in animal models of pulmonary inflammation Additionally MK-571 acts as a specific inhibitor of multidrug resistance protein 1 (MRP1) supporting its use in studies of leukotriene signaling and drug transport mechanisms
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Ambeed AMBEED
5000884423 NAPHTHALENE-18-DIOL 1G
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Medchemexpress LLC Naphthol AS-E | 92-78-4 | MFCD00021639 | 98.0% | 297.74 | C17H12ClNO2 | 1 ML
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Naphthol AS-E is a small-molecule inhibitor of the KIX-KID interaction that directly binds the KIX domain of CREB-binding protein (CBP). It is supplied as a solid or as a ready-to-use 10 mM solution in DMSO and is used in biochemical and cell-based assays to probe KIX-KID-mediated interactions.
- Potent, cell-permeable inhibitor of the KIX-KID interaction.
- Directly binds the KIX domain of CBP (reported Kd ≈ 8.6 μM).
- Available as solid or 10 mM solution in DMSO for ready use.
- High purity suitable for research applications.
- Stable under recommended storage conditions for powder and in solvent.
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Medchemexpress LLC SARS-CoV-2 S protein receptor-binding domain, biotinylated (Omicron B.1.1.529) | 96.0% | 50 UG
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Recombinant biotinylated receptor-binding domain (RBD) of the SARS-CoV-2 spike protein (Omicron B.1.1.529). Produced in HEK293 cells and supplied as a filtered PBS solution, this enzymatically biotinylated RBD includes C-terminal His and Avi tags and is intended for binding assays, ELISA development, and antibody characterization.
- Expression system: HEK293 cells
- Biotinylation: site-specific Avi tag
- Formulation: 0.22 μm filtered PBS, pH 7.4
- Concentration: 0.54 mg/mL
- Purity: 96.0% by reducing SDS-PAGE
- Endotoxin: <1 EU/μg (LAL)
- Storage: store at -80°C; avoid repeated freeze-thaw
- Applications: ACE2 binding assays, ELISA, antibody characterization
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000723729 T-4-COPPER1 BI 25MG
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eMolecules 102153-48-0 | 6-Bromo-1-nitronaphthalene | MFCD01464122 | 1g
Pharmablock | 14-oxazepan-5-one | 25mg | 713714680 | PBZJ1049 | 10341-26-1 | MFCD02683091 | 115.132 | C5H9NO2
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Sigma Aldrich Fine Chemicals Biosciences N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride | 61714-27-0 | MFCD00012559 | 25MG
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide hydrochloride | Mol Wt: 377.33 | 61714-27-0 | MFCD00012559 | 25MG
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AdipoGen 1E-Iodo-hex-1-ene
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Chemical. CAS 16644-98-7. Formula C6H11I. MW 210.1. Synthetic. Building block for synthesis.
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AdipoGen Tetrafluoro-IBX
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Chemical. CAS 954373-95-6. Formula C7HF4IO4. MW 352. Synthetic. Convenient substitute of o-iodoxybenzoic acid IBX as an oxidant. FIBX is safer, has neutral properties behaves as an equivalent to IBX in the oxidation of alcohols to ketones or aldehydes in polar solvents and shows better solubility.
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AdipoGen 1E-Iodo-oct-1-ene
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Chemical. CAS 42599-17-7. Formula C8H15I. MW 238.1. Synthetic. Building block for synthesis.
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AdipoGen Tetrafluoro-IBX
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Chemical. CAS 954373-95-6. Formula C7HF4IO4. MW 352. Synthetic. Convenient substitute of o-iodoxybenzoic acid IBX as an oxidant. FIBX is safer, has neutral properties behaves as an equivalent to IBX in the oxidation of alcohols to ketones or aldehydes in polar solvents and shows better solubility.
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Ambeed AMBEED
5000887881 44-2-4-BROMOPHENYL-2-PHE 250MG
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Ambeed AMBEED
5000889018 R-TERT-BUTYL 1-NAPHTHALE 100MG
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Cayman Chemical 4-hydroxy Chalcon 10g
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A chalcone metabolite; estrogenic and cytotoxic in MCF-7 cells at concentrations higher than 100 nM; inhibits TNF-α-induced NF-κB signaling and the trypsin-, chymotrypsin-, and caspase-like proteolytic activities of the 26S proteasome in K562 cells in a dose-dependent manner; reduces growth of K562, U937, and Jurkat cancer cell lines in a dose-dependent manner without effecting viability of PBMCs; inhibits GSH-RD (IC50 = 47.3 μM) in vitro in a reversible and non-competitive manner
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Aobchem AOBCHEM
5000872627 ETHYL 2- NAPHTHALEN-1-YL BENZO
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