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Filtered Search Results
eMolecules 938-73-8 | 2-Ethoxybenzamide | Oakwood Chemicals | MFCD00007977 | 165.192 | C9H11NO2 | 97.000 | CCOc1ccccc1C(N)=O | 5g | 480149412
2-Ethoxybenzamide | Oakwood Chemicals | 938-73-8 | MFCD00007977 | 165.192 | C9H11NO2 | 97.000 | CCOc1ccccc1C(N)=O | 5g | 480149412
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Medchemexpress LLC HY-117113 5mg Medchemexpress, JI051 CAS:2234281-75-3 Purity:>98%
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Medchemexpress, HY-117113 5mg JI051 CAS:2234281-75-3 JI051 is a stabilizer for the Hes1-PHB2 interaction, interacts with a cancer-associated protein chaperone prohibitin 2 ( PHB2 ), induces cell-cycle arrest by inhibiting the Notch downstream effector gene Hes1. Anti-cancer activity [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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Medchemexpress LLC HY-N0693 10mg Medchemexpress, Schisandrin A CAS:61281-38-7 Purity:>98%
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Medchemexpress, HY-N0693 10mg Schisandrin A CAS:61281-38-7 Schisandrin A inhibits CYP3A activity with an IC 50 of 6.60 μM and K i of 5.83 μM, respectively. 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 Mesdopetam hemitartrate | 2562346-14-7 | 99.86% | 350.39 | 50 MG
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Mesdopetam (IRL790) hemitartrate is a dopamine D3 receptor antagonist with psychomotor stabilizing properties, exhibiting a Ki of 90 nM and an IC50 of 9.8 μM for the human recombinant D3 receptor. It is utilized in research for motor and psychiatric complications associated with Parkinson disease.
- Dopamine D3 receptor antagonist
- Psychomotor stabilizing properties
- Used for research of motor and psychiatric complications in Parkinson disease
- Exhibits a Purity of 99.86%
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eMolecules 1527503-11-2 | Medchem Express | A-366 | 5mg | 446261511 | HY-12583 | MFCD28133403 | 329.444 | C19H27N3O2
Ambeed | 25-Di(thiophen-2-yl)thieno[32-b]thiophene | 250mg | 586036433 | A703648 | 21210-90-2 | MFCD11114556 | 304.460 | C14H8S4
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Medchemexpress LLC PND-1186 hydrochloride | 1356154-94-3 | 99.9% | 537.96 | 50 MG
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PND-1186 hydrochloride is a potent, highly-specific, and reversible inhibitor of FAK with an IC50 of 1.5 nM. It selectively promotes tumor cell apoptosis.
- Potent, highly-specific, and reversible FAK inhibitor.
- IC50 of 1.5 nM for FAK.
- Selectively promotes tumor cell apoptosis.
- Inhibits FAK Tyr-397 phosphorylation in breast carcinoma cells.
- Reduces tumor growth by inducing apoptosis in vivo.
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Medchemexpress LLC HY-100409 5mg Medchemexpress, PHCCC CAS:179068-02-1 Purity:>98%
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Medchemexpress, HY-100409 5mg PHCCC CAS:179068-02-1 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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Medchemexpress LLC MD2-TLR4-IN-1 | 2249801-12-3 | 98.2% | 10 MG
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MD2-TLR4-IN-1 is a myeloid differentiation protein 2/toll-like receptor 4 (MD2-TLR4) complex antagonist. It inhibits Lipopolysaccharides (LPS)-induced expression of TNF-α and IL-6 in macrophages with IC50 values of 0.89 μM and 0.53 μM, respectively. This compound can be utilized for the study of acute lung injury (ALI).
- Exerts anti-inflammatory activity by inhibiting NF-κB in RAW264.7 macrophages.
- Directly binds to the MD2-TLR4 complex and disrupts MD2-TLR4 activation.
- Suppresses NF-κB p65 subunit nuclear levels in LPS-induced macrophages.
- Significantly inhibits macrophage infiltration and ameliorates histopathological changes in lung tissues.
- Effectively reduces airspace inflammation and amends pulmonary lobule tissue structure.
- Decreases LPS-induced myeloperoxidase (MPO) activity and serum TNF-α levels.
- Reduces mRNA levels of TNF-α, IL-6, IL-1β, IL-12, IL-33, and COX-2 in lung tissues.
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Medchemexpress LLC HY-109096 5mg Medchemexpress, Nidufexor CAS:1773489-72-7 Purity:>98%
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Medchemexpress, HY-109096 5mg Nidufexor CAS:1773489-72-7 Nidufexor is a farnesoid X receptor (FXR) agonist [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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Medchemexpress LLC 3(2H)-Pyridazinone, 2,4-dimethyl-6-[1-[(1S)-1-phenylethyl]-6-(tetrahydropyran-4-yl)-1H-imidazo | 1660117-38-3 | 98.8% | 429.51 g/mol | C25H27N5O2 | 5 MG
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BRD4 Inhibitor-10 is a potent small-molecule inhibitor selective for the BD1 bromodomain of BRD4 (reported IC50 8 nM). Provided as a 5 mg solid research reagent, its chemical identifiers include CAS 1660117-38-3, formula C25H27N5O2, and molecular weight 429.51 g/mol. Supplier-reported purity is >98%.
- Potent BRD4-BD1 inhibition (IC50 8 nM).
- High purity suitable for biochemical and cellular assays.
- Well-defined small-molecule formula and molecular weight (C25H27N5O2; 429.51 g/mol).
- Supplied as a solid (5 mg) with solution formats available for immediate use.
- Intended for research use only; not for human or clinical use.
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eMolecules 2098969-71-0 | Medchem Express | DO34 analog | 5mg | 441681979 | HY-117771A | 531.536 | C26H28F3N5O4
Ambeed | 4-(2-Chloroacetyl)benzonitrile | 1g | 572861351 | A1038830 | 40805-50-3 | MFCD13172603 | 179.600 | C9H6ClNO
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Apexbio Technology LLC Chlorzoxazone 95-25-0 5g
Chlorzoxazone (CAS 95-25-0) is a small molecule that functions as a centrally acting skeletal muscle relaxant It exerts its pharmacological effects by modulating synaptic transmission within the spinal cord resulting in reduced muscle spasticity In biomedical research chlorzoxazone is frequently employed as a selective probe substrate for cytochrome P450 2E1 (CYP2E1) in human liver microsomes facilitating the assessment of hepatic CYP2E1 activity and drug metabolism This compound is valuable for investigating drug-drug interactions and metabolic profiling involving CYP2E1
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Medchemexpress LLC 1,3-dimethoxybenzene-d6 | 151-10-0 | MFCD00008384 | 98.0% | 10 MG
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1,3-dimethoxybenzene-d6 is the deuterated isotopologue of 1,3-dimethoxybenzene, provided as a research-scale labeled standard. Supplied at 98.0% purity in a 10 mg vial, it is intended for use in analytical workflows requiring deuterium labeling, such as mass spectrometry internal standards and tracer studies.
- Deuterated isotopologue for accurate mass spectrometry and tracer studies.
- High purity (98.0%) for reliable analytical performance.
- Small, convenient 10 mg package for research-scale use.
- Suitable as an internal standard for quantitative analysis.
- Stable aromatic compound compatible with common organic solvents.
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Medchemexpress LLC Tivozanib (hydrochloride hydrate) | 682745-41-1 | MFCD34184484 | >99.0% | 509.3 g/mol | C22H22Cl2N4O6 | 5 MG
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Tivozanib (hydrochloride hydrate) is the monohydrochloride monohydrate salt of tivozanib, a selective, orally active inhibitor of vascular endothelial growth factor receptors (VEGFRs). It is supplied for research and analytical applications, including in vitro biochemical and cellular assays.
- Selective VEGFR inhibitor suitable for target validation and signaling studies.
- Hydrochloride hydrate solid form for improved handling and stability.
- Reported high purity (>99%) from supplier analyses.
- Molecular formula C22H22Cl2N4O6; molecular weight 509.3 g/mol.
- Provided in small research quantities for assay development and SAR work.
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eMolecules 1037792-44-1 | Medchem Express | MBX-2982 | 5mg | 446265360 | HY-15291 | MFCD22628771 | 448.55 | C22H24N8OS
ChemScene | Morpholin-3-ylmethanol | 250mg | 572192195 | CS-0104915 | 106910-83-2 | MFCD04038650 | 117.148 | C5H11NO2
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