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Filtered Search Results
Aobchem 3-(Naphthalen-2-yl)benzaldehyde | ≥95% | CAS 728919-26-4 | C17H12O | 250mg
3-(Naphthalen-2-yl)benzaldehyde | ≥95% | CAS 728919-26-4 | C17H12O | 250mg
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Aobchem (5-Bromo-4-fluoro-2-methylphenyl)(methyl)sulfane | 97% | CAS 1416465-25-2 | C8H8BrFS | 250mg
(5-Bromo-4-fluoro-2-methylphenyl)(methyl)sulfane | 97% | CAS 1416465-25-2 | C8H8BrFS | 250mg
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Aobchem (3-Ethyl-4-fluoro-5-methylphenyl)(methyl)sulfane | 95% | CAS 2710913-24-7 | C10H13FS | 500mg
(3-Ethyl-4-fluoro-5-methylphenyl)(methyl)sulfane | 95% | CAS 2710913-24-7 | C10H13FS | 500mg
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Aobchem (3-Bromo-4-chloro-2-methylphenyl)boronic acid | 95% | C7H7BBrClO2 | 250mg
(3-Bromo-4-chloro-2-methylphenyl)boronic acid | 95% | C7H7BBrClO2 | 250mg
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Aobchem 3 5-Bis(methylthio)benzaldehyde | 97% | CAS 161922-07-2 | C9H10OS2 | 500mg
3 5-Bis(methylthio)benzaldehyde | 97% | CAS 161922-07-2 | C9H10OS2 | 500mg
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Medchemexpress LLC Laurolitsine (hydrochloride) | 50 MG
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Laurolitsine hydrochloride, also known as (+)-Norboldine hydrochloride, is an alkaloid derived from the leaves of *Peumus boldus* Molina. This compound exhibits weak anti-inflammatory activity and is intended for research use only. It has been shown to inhibit NO production in RAW 267.4 and BV-2 cells, and also remarkably inhibits the aggregation of rabbit platelets.
- Alkaloid isolated from *Peumus boldus* Molina leaves
- Exhibits weak anti-inflammatory activity
- Inhibits NO production in RAW 267.4 and BV-2 cells
- Inhibits aggregation of rabbit platelets
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Aobchem (5-Cyano-4-fluoro-2-methylphenyl)boronic acid | 95% | C8H7BFNO2 | 1g
(5-Cyano-4-fluoro-2-methylphenyl)boronic acid | 95% | C8H7BFNO2 | 1g
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Medchemexpress LLC Eflornithine (hydrochloride hydrate) | 96020-91-6 | 5 G
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Eflornithine hydrochloride hydrate (DFMO hydrochloride hydrate) is a specific, irreversible inhibitor of the enzyme ornithine decarboxylase. It is used in the treatment of African trypanosomiasis and excessive facial hair growth in women. This product is intended for research and analytical applications.
- For research and analytical applications
- Specific, irreversible inhibitor of ornithine decarboxylase
- Recommended storage for powder: 4°C, sealed, away from moisture
- Recommended storage for in solvent: -80°C for 6 months; -20°C for 1 month, sealed, away from moisture
- Shipping at room temperature if less than 2 weeks
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Aobchem 4-(4-Fluorobenzoyl)benzaldehyde | 95% | CAS 132307-97-2 | C14H9FO2 | 1g
4-(4-Fluorobenzoyl)benzaldehyde | 95% | CAS 132307-97-2 | C14H9FO2 | 1g
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Aobchem AOBCHEM
5000937784 6-BROMO-2-FLUORO-3-METHYLPHEN
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Aobchem (2-Bromo-6-fluoro-4-methylphenyl)(3 5-dimethylphenyl)methanol | 97% | CAS 3002543-36-1 | C16H16BrFO | 500mg
(2-Bromo-6-fluoro-4-methylphenyl)(3 5-dimethylphenyl)methanol | 97% | CAS 3002543-36-1 | C16H16BrFO | 500mg
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Aobchem AOBCHEM
5000944229 ETHYL 3-ISOBUTOXY-5-METHYLPHEN
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Aobchem (2-Bromo-6-fluoro-3-methylphenyl)(methyl)sulfane | ≥97% | CAS 1823520-30-4 | C8H8BrFS | 250mg
(2-Bromo-6-fluoro-3-methylphenyl)(methyl)sulfane | ≥97% | CAS 1823520-30-4 | C8H8BrFS | 250mg
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Medchemexpress LLC Pioglitazone hydrochloride | 112529-15-4 | 99.9% | C19H21ClN2O3S | 100 MG
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Pioglitazone hydrochloride (Standard) is the analytical standard for Pioglitazone hydrochloride. It is a potent and selective PPARγ agonist with EC50s of 0.93 and 0.99 μM for human and mouse PPARγ, respectively. This product is for research use only and not sold to patients.
- Analytical standard for Pioglitazone hydrochloride
- Potent and selective PPARγ agonist
- Used in qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
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Medchemexpress LLC Hydroxylamine, O-methyl-, hydrochloride (1:1) | 593-56-6 | MFCD00012951 | 98.0% | 83.52 | CH6ClNO | 100g
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Methoxyamine (O-Methylhydroxylamine) hydrochloride is an orally active and potent base excision repair (BER) inhibitor Methoxyamine hydrochloride binds to 3 hydroxyl groups that are left behind by 3-methylpurine-DNA glycosylase (MPG) following excision of the damaged base and thus inhibits BER activity Methoxyamine hydrochloride binds directly to the apyrimidinic (AP) sites Methoxyamine hydrochloride synergistically enhances the therapeutic efficacy of DNA-damaging agents[1][2]
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