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Filtered Search Results
Medchemexpress LLC Berberrubine chloride | 15401-69-1 | MFCD01658905 | 99.3% | 357.79 g/mol | C19H16ClNO4 | 50MG
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Berberrubine chloride is the chloride salt of berberrubine, an isoquinoline alkaloid and an active metabolite of berberine. Supplied as a solid reagent for research and analytical applications, it is commonly used in pharmacological, metabolic, and inflammation model studies. Product identifiers include CAS 15401-69-1, molecular formula C19H16ClNO4, and high purity appropriate for laboratory use.
- High purity (99.3%) suitable for analytical work.
- Verified molecular formula C19H16ClNO4 and molecular weight 357.79 g/mol.
- Intended for pharmacological and metabolic research applications.
- Supplied as a solid reference material for assays and profiling.
- Typical uses include inflammation model and metabolite studies.
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Apexbio Technology LLC YL-109 36341-25-0 10mM (in 1mL DMSO)
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YL-109 (CAS 36341-25-0) is a small molecule with demonstrated antitumor properties primarily acting through modulation of the aryl hydrocarbon receptor (AhR) signaling pathway This compound enhances expression of the molecular chaperone-associated ubiquitin ligase CHIP (C-terminus of Hsp70-interacting protein) leading to downstream regulation of processes implicated in cell proliferation and invasion In breast cancer models YL-109 induces CHIP expression resulting in suppressed proliferation and invasive capabilities of cancer cells YL-109 is thus a valuable tool for investigating AhR-mediated anticancer mechanisms and exploring therapeutic strategies in breast cancer research
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Medchemexpress LLC α-Methyltyrosine methyl ester hydrochloride | 7361-31-1 | MFCD00012606 | 98.9% | 245.71 | 5 G
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α-Methyltyrosine methyl ester hydrochloride is an orally active and competitive tyrosine hydroxylase inhibitor. It can inhibit the conversion of tyrosine to dopamine. It causes kidney damage and urethral calculi in rats and can be used as a tool for sympathetic nervous system research.
- Orally active
- Competitive tyrosine hydroxylase inhibitor
- Inhibits the conversion of tyrosine to dopamine
- Can be used as a tool for sympathetic nervous system research
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eMolecules 89711-08-0 | t-Butyl N-(2-oxoethyl)cabamate | Ochem Incorporation | MFCD01321273 | 159.185 | C7H13NO3 | 95.000 | CC(C)(C)OC(=O)NCC=O | 5g | 772471658
t-Butyl N-(2-oxoethyl)cabamate | Ochem Incorporation | 89711-08-0 | MFCD01321273 | 159.185 | C7H13NO3 | 95.000 | CC(C)(C)OC(=O)NCC=O | 5g | 772471658
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eMolecules 61074-71-3 | Ambeed | 3-Bromo-5-chloro-2-methylthiophene | 1g | 599118107 | A1452997 | MFCD19687381 | 211.5 | C5H4BrClS
Ambeed | 3-Bromo-5-chloro-2-methylthiophene | 1g | 599118107 | A1452997 | 61074-71-3 | MFCD19687381 | 211.500 | C5H4BrClS
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Medchemexpress LLC MET kinase-IN-4 | 888719-03-7 | 99.0% | 458.42 | 50 MG
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MET kinase-IN-4 is an orally active Met kinase inhibitor with potent Met kinase inhibitory activity (IC50 = 1.9 nM). It also inhibits Flt-3 and VEGFR-2 kinases. This compound shows good metabolic stability and can be used for cancer research. It exhibits a favorable pharmacokinetic profile in mice and demonstrates significant antitumor activity in the GTL-16 human gastric carcinoma xenograft model.
- Orally active Met kinase inhibitor
- Potent Met kinase inhibitory activity (IC50 = 1.9 nM)
- Inhibits Flt-3 and VEGFR-2 kinases
- Good metabolic stability in human and mouse liver microsomes
- Suitable for cancer research
- Exhibits favorable pharmacokinetic profile in mice
- Demonstrates significant antitumor activity in GTL-16 human gastric carcinoma xenograft model
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000369851 YL-365 25MG
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Medchemexpress LLC (2-Butyl-5-nitrobenzofuran-3-yl)(4-hydroxyphenyl)methanone | 141645-16-1 | 99.6% | C19H17NO5 | 5 G
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(2-Butyl-5-nitrobenzofuran-3-yl)(4-hydroxyphenyl)methanone is a drug intermediate for the synthesis of various active compounds. It is for research use only.
- Drug intermediate for synthesis of various active compounds.
- For research use only.
- Molecular weight: 339.35
- Formula: C19H17NO5
- CAS number: 141645-16-1
- Appearance: Solid
- Color: Off-white to yellow
- Purity: 99.6%
- Store powder at -20°C for 3 years; 4°C for 2 years.
- Store in solvent at -80°C for 6 months; -20°C for 1 month.
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eMolecules 1234217-58-3 | Methyl 2-(2-Bromo-4-pyridyl)acetate | MFCD18255863 | 1g
Ambeed | N3N53-Trimethyl-4-(((2R3S4S5S6R)-345-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-[11-biphenyl]-35-dicarboxamide | 5mg | 534567997 | A352670 | 1373346-85-0 | 460.483 | C23H28N2O8
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eMolecules EMOLECULES INC
5000496027 1-TERT-BUTOXYCARBONYLPI 10G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770747 3 5-DIPYRIDIN-3-YL 5G
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Medchemexpress LLC TH-6 | 3031349-25-1 | 95.0% | 429.44 | C22H24FN3O5 | 10 MG
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TH-6 is a potent histone deacetylase (HDAC) inhibitor intended for research applications. It inhibits multiple HDAC isoforms, induces apoptosis, causes G2/M cell cycle arrest, and demonstrates antiproliferative and antitumor activity in preclinical models.
- Potent HDAC inhibition with submicromolar to low micromolar IC50s.
- Inhibits cell migration and invasion in cancer cell models.
- Induces apoptosis and G2/M phase cell cycle arrest.
- Inhibits tubulin polymerization (IC50 4.06 μM) and increases acetylated α-tubulin and histone H3 levels.
- Supplied as a light yellow to khaki solid with 95.0% purity.
- Molecular weight 429.44; formula C22H24FN3O5; CAS 3031349-25-1.
- Soluble in DMSO at 50 mg/mL (requires warming and sonication).
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770876 N 1-DIPYRIDIN-4-YL 25G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000770897 TERT-BUTYL 4-3-AMIN 250MG
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5000771157 1 2-DIPYRIDIN-4-YL 10G
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