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Filtered Search Results
eMolecules 837422-57-8 | Medchem Express | WH-4-023 | 5mg | 446260993 | HY-12299 | MFCD28138072 | 568.678 | C32H36N6O4
Medchem Express | WH-4-023 | 5mg | 446260993 | HY-12299 | 837422-57-8 | MFCD28138072 | 568.678 | C32H36N6O4
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Medchemexpress LLC HY-15643A 5mg Medchemexpress, LY 303511 (hydrochloride) CAS:2070014-90-1 Purity:>98%
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Medchemexpress, HY-15643A 5mg LY 303511 (hydrochloride) CAS:2070014-90-1 LY 303511 hydrochloride is a structural analogue of LY294002. LY303511 does not inhibit PI3K. LY303511 enhances TRAIL sensitivity of SHEP-1 neuroblastoma cells. LY303511 reversibly blocks K+ currents (IC50=64.6±9.1 μM) in MIN6 insulinoma cells. 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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Aobchem 4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 1g
4-Ethoxy-1 2-dimethoxybenzene | ≥97% | CAS 41827-16-1 | C10H14O3 | 1g
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Aobchem 4-Phenoxy-2-(trifluoromethyl)phenylboronic acid pinacol ester | ≥97% | CAS 1196396-64-1 | C19H20BF3O3 | 500mg
4-Phenoxy-2-(trifluoromethyl)phenylboronic acid pinacol ester | ≥97% | CAS 1196396-64-1 | C19H20BF3O3 | 500mg
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Selleck Chemical LLC Phenoxybenzamine HCl S2499-50mg
Phenoxybenzamine HCl (NSC 37448 NCI-c01661) is a non-specific irreversible alpha antagonist with an IC50 of 550 nM
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Selleck Chemical LLC Mardepodect (PF-2545920) S2687-5mg
Mardepodect (PF-2545920) is a potent and selective PDE10A inhibitor with IC50 of 0 37 nM with 1000-fold selectivity over the PDE
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Medchemexpress LLC HY-19835 5mg Medchemexpress, LY2922470 CAS:1423018-12-5 Purity:>98%
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Medchemexpress, HY-19835 5mg LY2922470 CAS:1423018-12-5 LY2922470 is a potent, selective and orally available agonist of the G protein-coupled receptor 40 (GPR40), with EC50s of 7 nM, 1 nM and 3 nM for human GPR40, mouse GPR40 and rat GPR40, respectively. LY2922470 reduces glucose levels along with significant increases in insulin and GLP-1, is potential for the treatment of type 2 diabetes mellitus (T2DM). 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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eMolecules 682745-41-1 | Medchem Express | Tivozanib (hydrochloride hydrate) | 5mg | 719835616 | HY-10977A | 509.34 | C22H22Cl2N4O6
Medchem Express | Tivozanib (hydrochloride hydrate) | 5mg | 719835616 | HY-10977A | 682745-41-1 | 509.340 | C22H22Cl2N4O6
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Medchemexpress LLC HY-114157 10mg Medchemexpress, DO-264 CAS:2301866-59-9 Purity:>98%
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Medchemexpress, HY-114157 10mg DO-264 CAS:2301866-59-9 DO-264 is a selective and in vivo-active inhibitor of Abhydrolase Domain Containing 12 (ABHD12), with an IC50 of 11 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 4-chloro-5-cyano-N-[2-(diethylamino)ethyl]-2-methoxybenzamide | 104391-26-6 | 99.7% | 346.25 | C15H21Cl2N3O2 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
Medchemexpress LLC 4-chloro-5-cyano-N-[2-(diethylamino)ethyl]-2-methoxybenzamide | 104391-26-6 | 99.7% | 346.25 | C15H21Cl2N3O2 | 100 MG
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CGP 25454A is a selective presynaptic dopamine autoreceptor antagonist used in neuroscience research to increase extracellular dopamine and acetylcholine levels. Supplied as a white to off-white solid, it is suitable for in vitro and in vivo studies; certificate of analysis and safety data sheet are available.
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Medchemexpress LLC Beta-asarone (standard) | 5273-86-9 | MFCD00009281 | 99.8% | 208.25 g/mol | C12H16O3 | 10 MG
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Beta-asarone is an analytical standard intended for research and analytical applications. It is a neuroprotective phenylpropanoid provided with quality documentation for analytical use.
- Analytical standard suitable for research and analytical applications.
- High-purity reference material (≈99.8%).
- Molecular formula C12H16O3; molecular weight 208.25 g/mol.
- Supplied in small pack sizes for analytical use, e.g., 10 mg.
- Used in studies of neuroprotection and modulation of α-synuclein.
- Certificate of analysis (COA) and safety data sheet (SDS) available.
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Medchemexpress LLC (R)-Apremilast | 608141-44-2 | 100.0% | 460.50 g/mol | C22H24N2O7S | 10 MG
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(R)-Apremilast is the R-enantiomer of apremilast provided as a high-purity analytical standard for research use only. It is supplied as a white to yellow solid and can be provided as a solid or as a 10 mM solution in DMSO; safety and analytical documentation are available.
- Purity 99.99% (analytical grade).
- CAS number 608141-44-2.
- Molecular formula C22H24N2O7S.
- Molecular weight 460.50 g/mol.
- Available as solids (5 mg-500 mg) and 10 mM DMSO solutions.
- Intended for research use only, not for human or animal therapeutic use.
- Datasheet, COA, and SDS available for handling and analysis.
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eMolecules 870483-87-7 | GW2580 | AstaTech | MFCD12024701 | 366.421 | C20H22N4O3 | 95.000 | COc1ccc(COc2ccc(Cc3cnc(N)nc3N)cc2OC)cc1 | 1g | 601098372
GW2580 | AstaTech | 870483-87-7 | MFCD12024701 | 366.421 | C20H22N4O3 | 95.000 | COc1ccc(COc2ccc(Cc3cnc(N)nc3N)cc2OC)cc1 | 1g | 601098372
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Medchemexpress LLC Phenoxybenzamine hydrochloride | 63-92-3 | 99.5% | 500 MG
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Phenoxybenzamine hydrochloride is a nonselective, irreversible, and orally active alpha-adrenoceptor antagonist. It is utilized in research concerning hypertension, particularly when caused by pheochromocytoma, and has demonstrated antitumor activity. This compound also exhibits significant biological activity in various in vitro and in vivo studies.
- Nonselective and irreversible alpha-adrenoceptor antagonist
- Orally active compound
- Used in hypertension research for pheochromocytoma
- Exhibits antitumor activity
- Inhibits cell proliferation, migration, and invasion
- Activates LINGO-1 and inhibits the TrkB-Akt pathway
- Prevents hippocampal cell death after oxygen glucose deprivation
- Shows anti-tumorigenic effects in tumor models
- Provides neuroprotective benefits in traumatic brain injury models
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Medchemexpress LLC Jak-in-5 (hydrochloride) | 2751323-21-2 | 99.5% | 511.03 | 100 MG
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JAK-IN-5 hydrochloride is an inhibitor of JAK, extracted from patent US20170121327A1, compound example 283. It is for research use only.
- Inhibits STAT6 phosphorylation by 60% in IL-13-induced lung tissue in a mouse model of pSTAT6 induction.
- Inhibits 88% of BALF eosinophils in male C57 mice model of Alternaria alternata-induced eosinophilic inflammation of the lung.
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