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Filtered Search Results
Medchemexpress LLC Broflanilide (Standard) | 1207727-04-5 | 98% | 663.28 | 50 MG
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Broflanilide (Standard) | 1207727-04-5 | 98% | 663.28 | 50 MG
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Medchemexpress LLC Ceftaroline | 189345-04-8 | 98.5% | 604.70 g·mol⁻¹ | C22H20N8O5S4 | 25 MG
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Ceftaroline (T-91825) is an N-phosphono-type cephalosporin and the active metabolite of the prodrug ceftaroline fosamil. It demonstrates activity against a broad spectrum of gram-positive and gram-negative bacteria and is supplied as a high-purity research reagent for antibacterial studies.
- High purity appropriate for analytical and in vitro biological assays.
- Active metabolite of ceftaroline fosamil with established antibacterial profile.
- Molecular formula C22H20N8O5S4; molecular weight 604.70 g·mol⁻¹.
- Suitable for research on gram-positive and gram-negative pathogens.
- Supplied as a small-quantity research pack for assay development and characterization.
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Chemscene ChemScene | (R)-Tetrahydrofuran-2-yl-methylamine | 10G | CS-W011317 | 0.98 | 7202-43-9| MFCD00192476 | 101.15
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ChemScene | (R)-Tetrahydrofuran-2-yl-methylamine | 10G | CS-W011317 | 0.98 | 7202-43-9| MFCD00192476 | 101.15
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Medchemexpress LLC Cleistanthin B | 30021-77-3 | 98.2% | 542.49 | 1 MG
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Cleistanthin B is an orally active arylnaphthalene lignan lactone glycoside that demonstrates anti-SARS-CoV-2 effects in Vero cells and exhibits antitumor, diuretic, and antihypertensive properties in vivo.
- Exhibits anti-SARS-CoV-2 effects in Vero cells with an EC50 of 6.51 μM
- Shows no cytotoxicity to Vero cells in concentrations up to 100 μM
- Demonstrates antitumor activity against EAC and DAL tumor mice
- Also shows diuretic and antihypertensive effects
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Medchemexpress LLC Rhamnocitrin | 569-92-6 | 300.26 | 5 MG
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Rhamnocitrin is an anti-inflammatory and antioxidant agent that targets STIM-1, NFATc3, and MAPK pathways. It selectively inhibits oxidative stress and inflammatory responses in vascular endothelial cells and neurons by regulating miR-185, STIM-1, NFATc3, and ERK/p38 MAPK pathways. It can be used in the study of endothelial-related inflammatory diseases and neuroprotection.
- Functions as an anti-inflammatory and antioxidant agent.
- Targets STIM-1, NFATc3, and MAPK pathways.
- Inhibits oxidative stress and inflammatory responses.
- Useful for studying endothelial-related inflammatory diseases.
- Useful for neuroprotection research.
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Medchemexpress LLC Hinokiflavone | 19202-36-9 | 5 MG
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Hinokiflavone | 19202-36-9 | 5 MG
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Medchemexpress LLC Tabersonine | 4429-63-4 | MFCD28140545 | 336.43 | 50 MG
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Tabersonine | 4429-63-4 | MFCD28140545 | 336.43 | 50 MG
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Medchemexpress LLC Ro5-3335 | 30195-30-3 | 99.5% | 259.69 | 10 MG
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Ro5-3335 | 30195-30-3 | 99.5% | 259.69 | 10 MG
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Medchemexpress LLC Tienilic acid (Ticrynafen) | 40180-04-9 | 99.7% | 331.18 | 5 MG
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Tienilic acid (Ticrynafen; ANP 3624) acts as a diuretic hypotensive agent, but it induces hepatotoxicity. It is converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
- Functions as a diuretic hypotensive agent.
- Known to induce hepatotoxicity.
- Converted into electrophilic metabolites by cytochrome P450 (CYP) in vitro.
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Medchemexpress LLC Metsulfuron-methyl (Standard) | 74223-64-6 | 50 MG
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Metsulfuron-methyl (Standard) is the analytical standard of Metsulfuron-methyl. This product is intended for research and analytical applications. Metsulfuron-methyl is a systemic sulfonylurea herbicide that has been widely used to control broadleaf weeds and annual grasses in rice, corn, wheat, and barley. Metsulfuron-methyl exhibits high herbicidal activity and low mammalian toxicity, with an LD50 for rats exceeding 5000 mg/kg.
- The compound is the grade of analytical standard, which is the reference standard supplied assay.
- It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
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eMolecules Medchem Express / (-)-Epiafzelechin / 5mg / 713705081 / HY-N0943 / / 24808-04-6 / MFCD20260428 / 274.272 / C15H14O5
Medchem Express / (-)-Epiafzelechin / 5mg / 713705081 / HY-N0943 / / 24808-04-6 / MFCD20260428 / 274.272 / C15H14O5
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Medchemexpress LLC Dalpiciclib | 5MG
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Dalpiciclib (SHR-6390) is an orally active and highly selective inhibitor of CDK4 and 6 with IC50 values of 12 4 nM and 9 9 nM respectively[1][2] Dalpiciclib shows antitumor activity against breast cancer and esophageal squamous cell carcinoma[1][2][3][4]
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Medchemexpress LLC (E)-1-(4-methoxyphenyl)-3-(4-morpholin-4-yl-6-nitroquinolin-2-yl)prop-2-en-1-one | 2313528-04-8 | 97.0% | C23H21N3O5 | 10MG
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hnRNPK-IN-1 is a small-molecule ligand that binds heterogeneous nuclear ribonucleoprotein K (hnRNPK), disrupting hnRNPK interaction with the c-myc promoter to inhibit c-myc transcription and induce apoptosis in cell-based assays. Binding affinities were measured by SPR and MST, and the compound is supplied as a solid for research use.
- Binds hnRNPK and disrupts hnRNPK-c-myc promoter interaction.
- Inhibits c-myc transcription and induces apoptosis in HeLa cell assays.
- Measured binding affinities: SPR Kd 4.6 μM, MST Kd 2.6 μM.
- High purity (97.0%) solid, brown to orange in appearance.
- Soluble in DMSO (~5 mg/mL) with warming and sonication.
- Store powder at -20°C (long-term) and solvent solutions at -80°C when possible.
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Medchemexpress LLC Az12601011 | 2748337-86-0 | 99.8% | 50 MG
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AZ12601011 is an orally active, selective TGFBR1 kinase inhibitor (also inhibits ALK4 and ALK7) used as a research reagent to study TGF-β signaling and tumor models. It inhibits SMAD2 phosphorylation with reported potency (IC50 18 nM; Kd 2.9 nM) and has shown antitumor activity in vivo. High-purity powder and DMSO stock solutions are available.
- Selective TGFBR1, ALK4, and ALK7 inhibition.
- Biochemical potency: IC50 18 nM; Kd 2.9 nM.
- High purity (99.78%).
- Available as powder and DMSO solution for in vitro studies.
- Recommended storage: powder -20°C for long term, and solutions -80°C.
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eMolecules (3S,4S)-TETRAHYDROFURAN-3,4-DIOL | 84709-85-3 | | 1g
AstaTech | (3S,4S)-TETRAHYDROFURAN-3,4-DIOL | 1g | 112529505 | 66690 | 97.000 | 84709-85-3 | | 104.105 | C4H8O3
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