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Filtered Search Results
Aobchem 1-(2-(Isopentyloxy)phenyl)ethanone | ≥95% | CAS 101267-10-1 | C13H18O2 | 250mg
1-(2-(Isopentyloxy)phenyl)ethanone | ≥95% | CAS 101267-10-1 | C13H18O2 | 250mg
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Aobchem 5-Bromo-3-chloropicolinaldehyde | ≥97% | CAS 885168-04-7 | C6H3BrClNO | 1g
5-Bromo-3-chloropicolinaldehyde | ≥97% | CAS 885168-04-7 | C6H3BrClNO | 1g
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Aobchem 1-(2-(Isopentyloxy)phenyl)ethanone | ≥95% | CAS 101267-10-1 | C13H18O2 | 1g
1-(2-(Isopentyloxy)phenyl)ethanone | ≥95% | CAS 101267-10-1 | C13H18O2 | 1g
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Aobchem 5-Bromo-N N 2 4-tetramethylbenzamide | ≥97% | CAS 2734772-91-7 | C11H14BrNO | 250mg
5-Bromo-N N 2 4-tetramethylbenzamide | ≥97% | CAS 2734772-91-7 | C11H14BrNO | 250mg
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Aobchem 5-Bromo-3-methylsulfonylpyridine | ≥97% | CAS 445491-71-4 | C6H6BrNO2S | 1g
5-Bromo-3-methylsulfonylpyridine | ≥97% | CAS 445491-71-4 | C6H6BrNO2S | 1g
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Aobchem 2-Bromo-4 6-dimethylbenzaldehyde | 95% | CAS 88174-53-2 | C9H9BrO | 500mg
2-Bromo-4 6-dimethylbenzaldehyde | 95% | CAS 88174-53-2 | C9H9BrO | 500mg
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Aobchem 6-Bromo-2 4-dichlorophenylboronic acid | ≥97% | CAS 2121514-51-8 | C6H4BBrCl2O2 | 500mg
6-Bromo-2 4-dichlorophenylboronic acid | ≥97% | CAS 2121514-51-8 | C6H4BBrCl2O2 | 500mg
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Aobchem 1-Bromo-2-methoxy-4-(methylsulfonyl)benzene | ≥97% | CAS 90531-98-9 | C8H9BrO3S | 1g
1-Bromo-2-methoxy-4-(methylsulfonyl)benzene | ≥97% | CAS 90531-98-9 | C8H9BrO3S | 1g
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Medchemexpress LLC Cyjohnphos | 247940-06-3 | 350.49 | 25 G
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Cyjohnphos is a biochemical reagent that can be used as a biological material or organic compound for life science related research. It is also utilized in combination with a nickel catalyst for Suzuki-Miyaura arylation of tertiary benzylic acetates with aryl boroxines to produce diaryl and triaryl quaternary stereocenters.
- Suitable for life science research
- Used as a biological material or organic compound
- Utilized in combination with a nickel catalyst for Suzuki-Miyaura arylation
- Produces diaryl and triaryl quaternary stereocenters
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Aobchem 1-Bromo-4-isobutoxy-2 5-dimethylbenzene | 97% | CAS 2901099-16-7 | C12H17BrO | 250mg
1-Bromo-4-isobutoxy-2 5-dimethylbenzene | 97% | CAS 2901099-16-7 | C12H17BrO | 250mg
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Aobchem 3-Bromo-5-isopropoxybenzaldehyde | ≥97% | CAS 1112210-83-9 | C10H11BrO2 | 1g
3-Bromo-5-isopropoxybenzaldehyde | ≥97% | CAS 1112210-83-9 | C10H11BrO2 | 1g
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Medchemexpress LLC Sodium tetraphenylborate | 143-66-8 | MFCD00011494 | 99.6% | 342.22 g/mol | C24H20BNa | 25 G
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Sodium tetraphenylborate is a tetraphenylboron salt used as a precipitating agent and laboratory reagent for ion-exchange, separations, and analytical applications. Its high purity and defined solubility profile support reproducible analytical workflows.
- High purity: 99.6%.
- Chemical formula C24H20BNa and molecular weight 342.22 g/mol.
- Soluble in DMSO (200 mg/mL); sparingly soluble in water (3.33 mg/mL with warming).
- Suitable for precipitating cations and routine analytical precipitations.
- Available in multiple package sizes for laboratory use.
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Apexbio Technology LLC Tranylcypromine hydrochloride 1986-47-6 10mM (in 1mL DMSO)
Tranylcypromine hydrochloride (CAS 1986-47-6) is a small molecule inhibitor that irreversibly targets monoamine oxidase (MAO) isoforms A and B demonstrating mechanism-based inhibition with Ki values of 101 9 M for MAO A and 16 M for MAO B and corresponding IC50 values of 2 3 M and 0 95 M Additionally tranylcypromine acts as a time-dependent irreversible inhibitor of lysine-specific demethylase 1 (LSD1) an amine oxidase homolog with structural similarities to MAOs exhibiting a Ki of 242 M and an IC50 of 20 7 M This compound is widely utilized in studies investigating MAO and LSD1 enzymatic functions epigenetic regulation and monoamine metabolism
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Aobchem N-ethylmethanesulfonamide | ≥95% | CAS 2374-62-1 | C3H9NO2S | 5g
N-ethylmethanesulfonamide | ≥95% | CAS 2374-62-1 | C3H9NO2S | 5g
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Medchemexpress LLC GM-60186 | 99.3% | 504.59 | 1 ML
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GM-60186 is a 5-HT receptor 2B (HTR2B) inhibitor with an IC50 of 257 nM. It significantly inhibits colorectal cancer proliferation and migration.
- Inhibits HTR2B with an IC50 of 257 nM.
- Demonstrates anti-colorectal cancer activity.
- In vitro, it effectively inhibits proliferation in colorectal cancer (CRC) cells (COLO-205, MC38, CT26, and Caco2 cells) at concentrations of 50-500 nM over 72 hours.
- Effectively inhibits colorectal cancer migration at 500 nM over 24-48 hours.
- In vivo, it significantly reduces tumor size and weight in xenograft mouse models at doses of 10-20 mg/kg, administered daily for 20 days.
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