Phenoxy compounds
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Filtered Search Results
eMolecules Medchem Express / l-Pindolol / 5mg / 783660330 / HY-100606 / / 26328-11-0 / MFCD00153863 / 248.326 / C14H20N2O2
Medchem Express / l-Pindolol / 5mg / 783660330 / HY-100606 / / 26328-11-0 / MFCD00153863 / 248.326 / C14H20N2O2
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Medchemexpress LLC LYP-IN-1 | 1404436-51-6 | MFCD34567163 | 99.8% | 501.91 g/mol | C28H20ClNO6 | 5 MG
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LYP-IN-1 is a potent, selective inhibitor of lymphoid tyrosine phosphatase used in biochemical and cellular studies to probe T-cell and mast cell signaling. The compound contains an alkyne moiety enabling copper-catalyzed azide-alkyne cycloaddition for probe development and labeling in chemical biology applications.
- Potent and selective LYP inhibition (Ki 110 nM; IC50 0.259 μM).
- Alkyne handle for copper-catalyzed click chemistry applications.
- High purity suitable for biochemical and cellular assays.
- Soluble in DMSO up to 2 mg/mL with mild heating and sonication.
- Stable when stored as powder at -20°C for extended periods.
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Medchemexpress LLC GSK2945 hydrochloride | 00-00-0 | 99.7% | 457.80 g/mol | C20H19Cl3N2O2S | 5 MG
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GSK2945 hydrochloride is the hydrochloride salt of a small-molecule antagonist of the nuclear receptor Rev-erbα, supplied for preclinical research. It has reported EC50 values of 21.5 μM (mouse) and 20.8 μM (human) and has been used to increase CYP7A1 levels and modulate cholesterol metabolism.
- High chemical purity (99.7%).
- Solid form suitable for storage at 4°C; in solution store under nitrogen at -80°C (6 months) or -20°C (1 month).
- Soluble in DMSO (~20.83 mg/mL); in vivo formulations and protocols are available for suspension or clear solution preparations.
- Activity: Rev-erbα antagonist with reported EC50 around 21 μM in cell-based assays.
- Provided for research use with supporting assay and formulation data.
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eMolecules (S)-(1-Methylazetidin-2-yl)methanamine dihydrochloride | 2682097-49-8 | | 100mg
Ambeed | (S)-(1-Methylazetidin-2-yl)methanamine dihydrochloride | 100mg | 602849439 | A1328848 | | 2682097-49-8 | | 173.080 | C5H14Cl2N2
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eMolecules Medchem Express / AMTB (hydrochloride) / 5mg / 686921644 / HY-100345 / / 926023-82-7 / MFCD18086917 / 430.990 / C23H27ClN2O2S
Medchem Express / AMTB (hydrochloride) / 5mg / 686921644 / HY-100345 / / 926023-82-7 / MFCD18086917 / 430.990 / C23H27ClN2O2S
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![eMolecules Medchem Express / GW284543 / 5mg / 459606871 / HY-114189 / / 790186-68-4 / [null] / 372.424 / C23H20N2O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502449383.PNG-250.jpg)
eMolecules Medchem Express / GW284543 / 5mg / 459606871 / HY-114189 / / 790186-68-4 / [null] / 372.424 / C23H20N2O3
Medchem Express / GW284543 / 5mg / 459606871 / HY-114189 / / 790186-68-4 / [null] / 372.424 / C23H20N2O3
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![eMolecules Medchem Express / TX1-85-1 / 1mg / 455325840 / HY-100848 / / 1603845-32-4 / [null] / 580.693 / C32H36N8O3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502448642.PNG-250.jpg)
eMolecules Medchem Express / TX1-85-1 / 1mg / 455325840 / HY-100848 / / 1603845-32-4 / [null] / 580.693 / C32H36N8O3
Medchem Express / TX1-85-1 / 1mg / 455325840 / HY-100848 / / 1603845-32-4 / [null] / 580.693 / C32H36N8O3
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Medchemexpress LLC Arn 077 (URB913) | 1373625-34-3 | 98.8% | 50 MG
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ARN 077 (URB913) is a potent and selective N-acylethanolamine acid amidase (NAAA) inhibitor used as a research compound to modulate palmitoylethanolamide (PEA) levels in vitro and in vivo.
- Potent NAAA inhibition with low nanomolar activity.
- High purity (98.8%).
- Molecular formula C16H21NO4, molecular weight 291.34.
- Soluble in DMSO; in vitro solubility up to 250 mg/mL.
- Stable as a powder at -20°C for long-term storage.
- Supplied as a 50 mg solid for laboratory use.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000387884 VEGFR-2-IN-5 HYDROC 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000387818 4-PHENOXYBENZYLAMINE 10MM 1ML
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000353768 REDAFAMDASTAT 100MG
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Selleck Chemical LLC AST-487
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AST-487 (NVP-AST487) a N N -diphenyl urea is an ATP competitive inhibitor of Flt3 with ki of 0 12 M Besides FLT3 AST487 also inhibits RET KDR c-KIT and c-ABL kinase with IC50 values below 1 M
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Sigma Aldrich Fine Chemicals Biosciences CX546 >=98% (HPLC), solid | 215923-54-9 | MFCD01860868 | 50MG
CX546 >=98% (HPLC), solid | Purity: >=98% (HPLC) | Mol Wt: 247.29 | 215923-54-9 | MFCD01860868 | 50MG
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Chem-Impex International, Inc. Diphenyl phosphoryl azide | 26386-88-9 | MFCD00001987 | 250G
Diphenyl phosphoryl azide, 26386-88-9, MFCD00001987, 250G
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Selleck Chemical LLC ONO-4059 analogue
ONO-4059 analogue (ONO-WG-307) is an analogue of ONO-4059 which is a highly potent and selective oral BTK inhibitor with IC50 of 23 9 nM Phase 1
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