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Organic compounds that consist of five-membered heterocyclic molecules containing a nitrogen atom and at least one other non-carbon atom as part of the ring.
If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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If you are unable to find the chemical you are looking for, make sure you are logged into your fishersci.com account and click on the following link: eMolecules Building Block Tool
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6-Bromo-2-(bromomethyl)-3-fluoropyridine is a biological molecule intended for research use only. This compound is a white to off-white solid with a molecular formula of C6H4Br2FN and a molecular weight of 268.91.
Purity of 96.79%
Store at 4°C, protected from light
Soluble in DMSO at 100 mg/mL
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1-Bromo-4-(bromomethyl)benzene-d6 is a deuterium labeled compound, useful as a tracer or internal standard for quantitative analysis. Deuteration can influence pharmacokinetic and metabolic profiles of drugs, making this product valuable for drug development research.
Can be used as a tracer
Functions as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
Deuteration can affect the pharmacokinetic and metabolic profiles of drugs
For research use only
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1-Bromo-4-(bromomethyl)benzene-d6 is the deuterium labeled 1-Bromo-4-(bromomethyl)benzene. It can be used as a tracer or as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. Deuterium substitution can impact the pharmacokinetic and metabolic profiles of drugs.
Deuterium labeled compound
Used as a tracer or internal standard
Suitable for quantitative analysis by NMR, GC-MS, or LC-MS
Impacts pharmacokinetic and metabolic profiles of drugs
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PSN 375963 is a potent GPR119 agonist with EC50s of 8 4 and 7 9 M for human and mouse GPR119 respectively PSN 375963 shows similar potency to the endogenous agonist oleoylethanolamide (OEA)[1 [2
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ODQ (CAS 41443-28-1) is a selective inhibitor of soluble guanylate cyclase (sGC) interfering with nitric oxide (NO)-dependent intracellular signaling by blocking sGC-mediated catalysis of cyclic guanosine monophosphate (cGMP) synthesis This inhibition results in reduced cGMP production and subsequent modulation of protein kinase G-regulated cellular processes Studies have demonstrated that ODQ enhances cisplatin-induced apoptosis in human mesothelioma cells in vitro supporting its use in investigating tumor cell apoptosis mechanisms and evaluating synergistic effects in anticancer drug research
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