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Filtered Search Results
GRAINGER INC DIMETHYL MALEATE 500ML
502781740 DIMETHYL MALEATE 500ML
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Medchemexpress LLC AZD9496 maleate | 1639042-28-6 | 99.4% | 50 MG
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AZD9496 maleate is a potent and selective estrogen receptor (ERα) antagonist with an IC50 of 0.28 nM. It functions as an orally bioavailable selective estrogen receptor degrader (SERD), identified as a laboratory chemical.
- Potent and selective estrogen receptor (ERα) antagonist
- Orally bioavailable selective estrogen receptor degrader (SERD)
- Suitable for scientific research
- Used in signaling pathways
- For research use only
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Medchemexpress LLC Ro 25-6981 (Maleate) | 1312991-76-6 | 99.3% | 455.54 | 50 MG
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Ro 25-6981 Maleate is a potent, selective, and activity-dependent NR2B subunit-specific NMDA receptor antagonist. It demonstrates anticonvulsant and anti-parkinsonian activity and is considered to have potential for research into Parkinson's disease (PD).
- Potent, selective, and activity-dependent NR2B subunit-specific NMDA receptor antagonist
- Shows anticonvulsant activity
- Shows anti-parkinsonian activity
- Potential for Parkinson's disease (PD) research
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TARGETMOL CHEMICALS INC Monatepil maleate 1MG
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Also available in 5 mg, 10 mg, 25 mg, 50 mg and bulk. Please contact Fisher for quotes. Monatepil maleate (AJ-2615 maleate) is an orally active Ca2+-channel and alpha1-adrenoceptor antagonist and non-competitive heparanoyl-coenzyme Acholesterol acyltransferase (ACAT) inhibitor with antihypertensive activity.Monatepil maleate is used in studies of hyperlipidemia and atherosclerosis. Monatepil maleate is used to study hyperlipidemia and atherosclerosis. Purity 96.28%
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Medchemexpress LLC PD-168077 maleate | 630117-19-0 | 99.6% | 450.49 | 100 MG
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PD-168077 maleate is a selective dopamine D4 receptor agonist with a Ki of 9 nM. It is for research use only. It shows high selectivity over other D2-like receptor family members and D1-like counterparts, as well as α1, α2, 5-HT1A, and 5-HT2A receptors. It evidences intrinsic activity at the D4 receptor and can induce locomotion in a dose-dependent manner. This product may be used in research related to neurological diseases, neurodegenerative diseases, depression, and Parkinson's disease.
- Selective dopamine D4 receptor agonist
- High selectivity over other receptor types
- Evidences intrinsic activity at the D4 receptor
- Induces locomotion in PD-168077-treated cells
- May be used in research for neurological diseases
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Apexbio Technology LLC Mepyramine maleate 59-33-6 10mM (in 1mL DMSO)
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Mepyramine maleate (CAS 59-33-6) is a selective antagonist of the histamine H1 receptor exhibiting dissociation constants of 0 8 nM for H1 5200 nM for H2 and over 3000 nM for H3 receptors By blocking H1 receptor-mediated signaling it modulates pathways involved in allergic responses Mepyramine maleate is commonly utilized in experimental models of allergic diseases to investigate histamine-related mechanisms and to delineate the role of H1 receptor activity in immunological and inflammatory processes
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Medchemexpress LLC Arimoclomol maleate | 289893-26-1 | MFCD28143527 | ≥98.0% | 429.85 | C18H24ClN3O7 | 1 ML
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Arimoclomol maleate is the maleate salt of arimoclomol (BRX-220), an orally active co-inducer of heat shock proteins used in neuroscience and neurodegeneration research. The product is supplied as a ready-to-use 10 mM solution in DMSO (1 mL) for in vitro research; solid quantities are also available for custom preparation.
- Co-induces heat shock proteins to enhance protein quality control.
- Provided as a 10 mM solution in DMSO, 1 mL ready stock.
- Maleate salt form for improved stability and handling.
- High purity (≥98.0%).
- Molecular weight 429.85 g/mol and CAS 289893-26-1 for unambiguous identification.
- Storage: sealed at 4°C; in solution store at -80°C up to 6 months, -20°C up to 1 month.
- Available in solid masses (1 mg, 5 mg, 10 mg) for custom concentration preparation.
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Medchemexpress LLC Bgt226 maleate | 1245537-68-1 | MFCD22124895 | 99.9% | C32H29F3N6O6 | 10MG
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BGT226 maleate is a research-grade small-molecule inhibitor of class I PI3K isoforms and mTOR, used to probe PI3K/mTOR signaling in cellular and biochemical studies. The compound is supplied as a high-purity solid salt for laboratory research use only and is provided with recommended storage conditions and analytical quality data.
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Medchemexpress LLC ER-27319 maleate | 1204480-26-1 | 99.4% | 396.44 | 100 MG
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ER-27319 maleate is an acridone derivative, a potent and selective SYK inhibitor that inhibits the tyrosine phosphorylation of SYK and its activity. It inhibits the release of antigen-induced allergic mediators from human and rat mast cells with an IC50 of 10 μM, making it suitable for the study of allergic diseases.
- Inhibits antigen-induced generation of inositol phosphates
- Inhibits release of arachidonic acid
- Inhibits secretion of histamine and tumor necrosis factor α
- Selectively inhibits the tyrosine phosphorylation of SYK
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Medchemexpress LLC ST-148 maleate | 390803-40-4 | 99.4% | 612.74 | 1 MG
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ST-148 maleate is a potent and orally active DENV inhibitor. It demonstrates antiviral efficacy and low cell toxicity. ST-148 maleate works by altering the interaction between lipid droplets and the C protein, which in turn inhibits viral replication.
- Potent and orally active DENV inhibitor
- Demonstrates antiviral efficacy
- Low cell toxicity
- Inhibits viral replication
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Medchemexpress LLC Edonerpic (maleate) | 519187-97-4 | 99.8% | 407.48 | 200 MG
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Edonerpic maleate is a novel neurotrophic agent that can inhibit amyloid-β peptides (Aβ). It preserves cortical neurons in the presence of Aβ(1-42), prevents oxidative stress-induced neuronal death, and significantly increases neurite length. It also ameliorates deficits in adult neurogenesis and spatial memory.
- Novel neurotrophic agent
- Inhibits amyloid-β peptides (Aβ)
- Preserves cortical neurons in the presence of Aβ(1-42)
- Prevents oxidative stress-induced neuronal death at 0.1 and 1 μM
- Almost completely prevents GSH reduction at 0.1 and 1 μM
- Significantly increases neurite length at 0.1 and 1 μM
- Ameliorates deficits in adult neurogenesis and spatial memory in rats infused i.c.v. with amyloid-beta peptide
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Chemscene ChemScene | Methyl 5-hexenoate,98% (stabilized with MEHQ) | 10G | CS-0015919 | 98% (stabilized with MEHQ) | 2396-80-7| MFCD00671538 | 128.17
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ChemScene | Methyl 5-hexenoate,98% (stabilized with MEHQ) | 10G | CS-0015919 | 98% (stabilized with MEHQ) | 2396-80-7| MFCD00671538 | 128.17
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Sigma Aldrich Fine Chemicals Biosciences Perhexiline maleate salt 950MG
Perhexiline maleate regulatesnbspcoronary vasodilatation and blocks exercise-induced tachycardia. It is used to treat angina pectoris and variant angina. Perhexiline maleate functions as a cardiac metabolic agent. It is associated with peripheral neuropathy, high intracranial pressure withnbsppapilledemanbspand proximal myopathy.
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eMolecules 870646-83-6 | Ambeed | 4-(t-Butyldimethylsilyloxy)-23-difluorophenylboronic acid | 250mg | 718339529 | A507055 | MFCD18914502 | 288.17 | C12H19BF2O3Si
Ambeed | 4-(t-Butyldimethylsilyloxy)-23-difluorophenylboronic acid | 250mg | 718339529 | A507055 | 870646-83-6 | MFCD18914502 | 288.170 | C12H19BF2O3Si
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Apexbio Technology LLC WAY-100635 maleate salt 1092679-51-0 50mg
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WAY-100635 maleate salt (CAS 1092679-51-0) is a selective antagonist of the serotonin 5-HT1A receptor subtype It demonstrates high potency with a reported pIC50 value of 8 87 and displays over 100-fold selectivity relative to other serotonin receptor isoforms and common neurotransmitter receptor classes Due to its specific interaction with 5-HT1A receptors WAY-100635 maleate is frequently applied in neuroscience research to elucidate serotonin-mediated pathways and associated physiological or behavioral responses
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