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Filtered Search Results
Medchemexpress LLC 9(Z)-Octadecenedioic acid | 20701-68-2 | 99.4% | 312.44 | 500 MG
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9(Z)-Octadecenedioic acid is a C18 cutin monomer that acts as a marine biodegradation rate accelerator for synthesizing biodegradable resins and other materials. It is also a structural analog of 9,10,16-trihydroxyhexadecanoic acid.
- C18 cutin monomer
- Marine biodegradation rate accelerator
- Structural analog of 9,10,16-trihydroxyhexadecanoic acid
- Used for synthesizing biodegradable resins
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Medchemexpress LLC (Z)-Indirubin | 906748-38-7 | 262.26 | 100 MG
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(Z)-Indirubin is an isomer of Indirubin, a bis-indole alkaloid that has demonstrated anticancer activity against chronic myelocytic leukemia. This product is intended for research use only.
- Isomer of indirubin
- Bis-indole alkaloid
- Exhibits anticancer activity against chronic myelocytic leukemia
- Suitable for research use
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Medchemexpress LLC Benzyloxycarbonyl valacyclovir | 124832-31-1 | 98.1% | 458.47 | 5 G
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Cbz-Valaciclovir (Benzyloxycarbonyl valacyclovir) is a compound that can be utilized in the preparation of Valaciclovir and for antiviral research. This product is intended for research use only and is not available for sale to patients.
- Can be used to prepare Valaciclovir
- Applicable for antiviral research
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Medchemexpress LLC (Z)-9-Tricosene (cis-9-Tricosene) | 27519-02-4 | 98.0% | 322.61 | 100 MG
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(Z)-9-Tricosene (cis-9-Tricosene) is an insect pheromone present in flies of the order Diptera (such as the housefly) and can be used as an insecticide.
- Functions as an insect pheromone, specifically present in Diptera flies.
- Can be utilized as an insecticide.
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Medchemexpress LLC E/Z-Locostatin | 133812-16-5 | 99.52% | 245.27 | 50 MG
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E/Z-Locostatin is a racemic mixture of Locostatin. This potent RKIP inhibitor binds to Raf kinase inhibitor RKIP protein, disrupting its interaction with Raf-1 kinase and G protein-coupled receptor kinase 2. It inhibits cell proliferation and migration.
- Potent RKIP inhibitor
- Disrupts interaction of RKIP with Raf-1 kinase and G protein-coupled receptor kinase 2
- Inhibits cell proliferation
- Inhibits cell migration
- Aggravates thioacetamide-induced acute liver failure in mice
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Medchemexpress LLC Z-LEVD-FMK | 1135688-25-3 | 98.0% | 10 MG
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Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor that blocks ER stress-induced apoptosis in cancer cells. It inhibits IL-1β-induced IL-8 production in hRPE cells and caspase-3 activity in hRPE cells, and reverses E2-inhibited growth and prevents morphologic alterations associated with apoptosis in 5C cells.
- Blocks IL-1β-induced IL-8 production in hRPE cells.
- Inhibits caspase-3 activity in hRPE cells.
- Blocks E2-induced PARP cleavage in 5C cells.
- Reverses E2-inhibited growth and prevents morphologic alterations associated with apoptosis in 5C cells.
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Medchemexpress LLC Z-LEVD-FMK | 1135688-25-3 | 98.0% | 100 MG
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Z-LEVD-FMK is a cell-permeable caspase-4 inhibitor that effectively blocks ER stress-induced apoptosis in cancer cells.
- Cell-permeable caspase-4 inhibitor
- Blocks ER stress-induced apoptosis in cancer cells
- Purity of 98.0%
- Molecular weight: 652.71
- Chemical formula: C31H45FN4O10
- Appearance: solid, white to off-white
- Soluble in DMSO at 125 mg/mL
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In-solvent storage: -80°C for 6 months, -20°C for 1 month
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Medchemexpress LLC 11,14,17-eicosatrienoic acid, (11Z,14Z,17Z)- | 17046-59-2 | 99.3% | 306.48 | 50 MG
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11(Z),14(Z),17(Z)-Eicosatrienoic acid is an unsaturated fatty acid that can maintain the continued replication of functional mitochondria in *Saccharomyces cerevisiae* (KD115).
- Maintains the continued replication of functional mitochondria in *Saccharomyces cerevisiae* (KD115).
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Medchemexpress LLC (Z)-FeCP-oxindole | 1137967-28-2 | 99.6% | 329.17 | 10 MM * 1 ML
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(Z)-FeCP-oxindole is a selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor with an IC50 value of 200 nM. It can significantly inhibit VEGFR1 and PDGFRa or b at 10 μM. (Z)-FeCP-oxindole also exhibits anticancer activity, acting on B16 murine melanoma lines with an IC50 less than 1 μM.
- Selective human vascular endothelial growth factor receptor 2 (VEGFR2) inhibitor
- Inhibits VEGFR1 and PDGFRa or b
- Exhibits anticancer activity
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Medchemexpress LLC (Z)-3-ferrocenylmethylidene-1,3-dihydro-2H-indol-2-one | 1137967-28-2 | MFCD18252658 | 99.6% | 329.17 g·mol⁻1 | C19H15FeNO | 5 MG
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(Z)-FeCP-oxindole is a small-molecule inhibitor that selectively targets vascular endothelial growth factor receptor 2 (VEGFR2). It inhibits VEGFR2 with an IC50 of 200 nM, shows additional activity against VEGFR1 and PDGFR isoforms at higher concentrations, and has demonstrated anticancer activity in cellular models. The compound is supplied as a solid powder and as a DMSO stock solution for research use.
- Selective VEGFR2 inhibitor with IC50 of 200 nM.
- Activity against VEGFR1 and PDGFRα/β at higher concentrations.
- Demonstrated anticancer activity in cellular models.
- Supplied as solid powder and as DMSO stock solution.
- High purity (≈99.6%) suitable for research applications.
- Stable when stored under recommended temperature conditions.
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eMolecules 2-Cbz-amino-ethanesulfonic acid | 119225-23-9 | MFCD04114348 | 500mg
J & W PharmLab LLC | 2-Cbz-amino-ethanesulfonic acid | 500mg | 452541077 | 05R0037 | 97.000 | 119225-23-9 | MFCD04114348 | 259.280 | C10H13NO5S
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Medchemexpress LLC Cis-aconitic acid | 585-84-2 | MFCD00063184 | 99.3% | 174.11 g/mol | C6H6O6 | 10 MG
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(Z)-Aconitic acid (cis-aconitic acid) is the Z-isomer of aconitic acid provided as a research-grade analytical standard for biochemical and analytical applications. It serves as a reagent and reference compound in enzymology, metabolic profiling, and chromatographic method development. The compound has CAS 585-84-2, formula C6H6O6, and molecular weight 174.11 g/mol.
- High purity suitable for analytical use.
- Verified by RP-HPLC for assay confirmation.
- Appropriate as an enzymology and metabolomics standard.
- Small pack sizes for lab-scale experiments.
- Crystalline material with defined molecular weight for accurate calculations.
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Medchemexpress LLC S -3-N-Cbz-Amino-su 5g
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(S)-3-N-Cbz-Amino-succinimide (Compound 1d) is an antiepileptic agent that can inhibit pentylenetetrazole (PTZ) and maximal electroshock (MES)-induced tonic convulsions in mice[1]
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Medchemexpress LLC (Z)-10-hydroxynortriptyline | 47132-19-4 | 99.7% | 279.38 g·mol⁻¹ | C19H21NO | 5 MG
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(Z)-10-Hydroxynortriptyline is a research-grade metabolite of nortriptyline supplied as a solid reference standard for analytical and biochemical studies. It is intended for laboratory research use only and not for human or veterinary applications.
- CAS number: 47132-19-4.
- Molecular formula: C19H21NO.
- Molecular weight: 279.38 g·mol⁻¹.
- Purity: 99.7%.
- Physical form: white to off-white solid.
- Available in small research pack sizes (e.g., 5 mg).
- Supplied for laboratory research use only.
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Medchemexpress LLC Semaxanib | 194413-58-6 | MFCD09763655 | 238.29 g·mol⁻1 | C15H14N2O | 250 MG
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(Z)-Semaxanib, also known as SU5416 or Semaxanib, is a small-molecule tyrosine kinase inhibitor used for laboratory research. It inhibits VEGFR and related receptor tyrosine kinases and has reported cytotoxic activity in hepatic cell lines. The compound is provided as a powder with documented storage recommendations for long-term stability.
- Small-molecule tyrosine kinase inhibitor targeting VEGFR and c-Met.
- Shows cytotoxicity in TAMH and HepG2 cells (IC50 6.28 μM and 8.17 μM).
- Chemical formula C15H14N2O; molecular weight 238.29 g·mol⁻1.
- Supplied as a powder suitable for research applications.
- Storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (6 months) or -20°C (1 month).
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