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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000293446 B7-H2/ICOSLG RAT H 50UG
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Medchemexpress LLC Acridine orange (hydrochloride) | 65-61-2 | MFCD00150070 | 99.7% | 301.81 g/mol | C17H20ClN3 | 1 ML
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Acridine Orange hydrochloride is a cell-permeable, nucleic acid-selective fluorescent dye used to differentially stain DNA and RNA. In solution it emits green fluorescence when bound to double-stranded DNA (~530 nm) and orange/red fluorescence when bound to single-stranded DNA or RNA (~640 nm). Commonly supplied as a 10 mM solution in DMSO for laboratory research use.
- Cell-permeable nucleic acid-selective fluorescent dye.
- Distinguishes double-stranded DNA (green) from single-stranded DNA/RNA (orange/red).
- Available as a 10 mM solution in DMSO (1 mL) or as a solid form.
- Suitable for fluorescence microscopy and flow cytometry applications.
- Molecular formula C17H20ClN3; molecular weight 301.81 g/mol.
- For research use only; not for human or clinical use.
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Medchemexpress LLC (S)-4-isopropyl-3-methyl-2-(3-methylpiperidine-1-carbonyl)isoxazol-5(2H)-one | 654059-21-9 | 99.8% | 266.34 g/mol | C14H22N2O3 | 100 MG
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BAY 59-9435 (HSL-IN-2) is a potent, selective small-molecule inhibitor of hormone-sensitive lipase (HSL) with an IC50 of 0.023 μM. It exhibits cellular activity (28 nM in 3T3-L1 cells for inhibition of forskolin-stimulated lipolysis) and is supplied as a high-purity solid for research use, with recommended storage conditions to maintain stability.
- Potent and selective HSL inhibition (IC50 0.023 μM).
- Demonstrated cellular activity in adipocyte assays (28 nM).
- High purity suitable for biochemical and cellular studies.
- Stable as powder under recommended storage conditions.
- Soluble in DMSO for assay preparation.
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Kyfora Bio Acridine orange 5g
Acridine orange is a nucleic acid-selective fluorescent cationic dye useful for cell cycle determination It emits green fluorescence (525 nm) when bound to dsDNA and red fluorescence (650 nm) when bound to ssDNA or RNA
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Medchemexpress LLC 4,6(1H,5H)-Pyrimidinedione, 1-(3-chloro-4-methylphenyl)-5-[3-(2-furanyl)-2-propen-1-ylidene] | 593273-05-3 | 99.2% | 372.83 | 25 MG
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DCH36_06 is a potent and selective p300/CBP inhibitor. It mediates p300/CBP inhibition, leading to hypoacetylation on H3K18 in leukemic cells, and exhibits anti-tumor activity.
- Potent and selective p300/CBP inhibitor.
- Induces apoptosis in leukemic cells.
- Arrests cell cycle at G1 phase.
- Shows potent antiproliferative activity against a range of leukemia cell lines.
- Blocks leukemic xenograft growth in mice.
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Medchemexpress LLC HCV-IN-31 | 1998705-62-6 | 99.7% | 312.30 | 1 ML
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HCV-IN-31 is a potent HCV inhibitor. It has an EC50/EC95 of 15.7 μM for HCV replicon, making it suitable for research applications related to hepatitis C virus inhibition.
- Functions as an HCV inhibitor
- Exhibits an EC50/EC95 of 15.7 μM for HCV replicon
- Solid appearance
- Color ranges from white to off-white
- Purity of 99.7%
- Molecular weight of 312.30
- Intended for research use only
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Medchemexpress LLC Bay 59-9435 | 654059-21-9 | 99.8% | 266.34 g·mol⁻¹ | C14H22N2O3 | 25 MG
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BAY 59-9435 is a potent, selective small-molecule inhibitor of hormone-sensitive lipase (HSL) with a reported IC50 of 0.023 μM. It is used as a research tool to study HSL-dependent lipolysis in cellular and animal models. Not for human or clinical use.
- Potent, selective inhibition of hormone-sensitive lipase.
- Low IC50 (0.023 μM) enabling submicromolar activity.
- High purity suitable for biochemical and cellular assays (99.8%).
- Characterized chemical profile (C14H22N2O3; MW 266.34 g·mol⁻¹).
- Convenient small pack size for preclinical research (25 mg).
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Medchemexpress LLC 2-morpholin-4-yl-6-thianthren-1-ylpyran-4-one | 587871-26-9 | 99.9% | 200MG
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2-morpholin-4-yl-6-thianthren-1-ylpyran-4-one | 587871-26-9 | 99.9% | 200MG
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Medchemexpress LLC Chelerythrine chloride | 3895-92-9 | 99.1% | 10 MG
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Chelerythrine chloride is a benzophenanthridine alkaloid supplied as a high-purity research reagent and a potent, cell-permeable inhibitor of protein kinase C (PKC) used in biochemical and cellular studies.
- High purity: 99.1% by HPLC.
- Potent inhibitor of protein kinase C and reported to interact with Bcl-xL.
- Supplied as a solid powder suitable for biochemical and cellular assays.
- Soluble in DMSO, limited solubility in water.
- Available in mg-scale packages, including 10 mg, for research use.
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Medchemexpress LLC Propanoic acid, 2-hydroxy-, compound with dovitinib (lactate) | 692737-80-7 | MFCD23103506 | 99.8% | 482.51 g/mol | C24H27FN6O4 | 200 MG
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Dovitinib lactate is the lactate salt of dovitinib, a multi-targeted tyrosine kinase inhibitor active at low nanomolar concentrations against FLT3, c-Kit, FGFR1/3, VEGFR1/2/3, and PDGFRα/β. Supplied as a light-yellow solid for research use, the product is provided in a 200 mg quantity and is intended for preclinical kinase and cell signaling studies.
- Multi-targeted tyrosine kinase inhibitor with low-nanomolar IC50s against FLT3, c-Kit, FGFR1/3, VEGFR1/2/3, and PDGFRα/β.
- Lactate salt form for improved handling and solubility.
- Molecular formula C24H27FN6O4; molecular weight 482.51 g/mol.
- Purity approximately 99.8% as reported by batch certificate of analysis.
- Soluble in DMSO (~25 mg/mL); use freshly opened DMSO due to hygroscopicity.
- Store sealed at 4°C and protect from moisture.
- For laboratory research use only; not for human or clinical use.
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Medchemexpress LLC Panobinostat | 404950-80-7 | MFCD09833242 | 99.4% | 349.43 | C21H23N3O2 | 200 MG
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Panobinostat is a potent, orally active, non-selective histone deacetylase (HDAC) inhibitor supplied as a research-grade powder for laboratory use. It exhibits antineoplastic activity and is commonly used in epigenetic and cancer research, and in studies of apoptosis and autophagy. Not for human or veterinary use.
- Potent non-selective HDAC inhibitor with antineoplastic activity.
- High purity (99.4% by LCMS).
- Powder form, soluble in DMSO ≥ 100 mg/mL.
- Storage: powder -20°C (3 years) or 4°C (2 years); in solvent -80°C (1 year).
- Used in studies of apoptosis, autophagy, and cancer cell proliferation.
- Intended for research use only; not for human or veterinary use.
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Medchemexpress LLC Poly(oxy-1,2-ethanediyl), α-(2-aminoethyl)-ω-methoxy- | 80506-64-5 | 98.0% | (C2H4O)nC3H9NO | 50 MG
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mPEG-amine (MW 20000) is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker: one for an E3 ubiquitin ligase and the other for the target protein. These compounds exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. This product is for research use only.
- PEG-based PROTAC linker
- Useful in the synthesis of PROTACs
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
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Medchemexpress LLC N6-(2-phenylethyl)adenosine | 20125-39-7 | MFCD00055128 | 99.4% | 371.39 g/mol | C18H21N5O4 | 200 MG
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N6-(2-Phenylethyl)adenosine is an adenosine derivative provided as a research-grade small molecule for studies of adenosine receptor pharmacology. It is supplied as a white to off-white solid with high reported purity and is intended for laboratory research use.
- CAS number 20125-39-7.
- Molecular formula C18H21N5O4.
- Molecular weight 371.39 g/mol.
- Purity 99.4%.
- Physical form white to off-white solid.
- Pack size 200 mg.
- Storage powder: -20°C (3 years) or 4°C (2 years); in solvent: -80°C (2 years) or -20°C (1 year).
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Medchemexpress LLC Mpeg-amine (MW 2000) | 80506-64-5 | 99.6% | (C2H4O)nC3H9NO | 50 MG
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mPEG-amine (MW 2000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. This product is for research use only.
- Acts as a PEG-based PROTAC linker
- Utilized in the synthesis of PROTACs
- Suitable for biochemical assay reagents
- Applicable in drug delivery
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Medchemexpress LLC Idra 21 200Mg | HY-101528-200MG
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Idra 21 200Mg
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