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Organic compounds with acidic properties, and will commonly have carboxylic acids or similar functional groups in their structure. Derived compounds are also included.
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Sodium-dodecyl sulfate-d25 is a deuterium labeled Sodium dodecyl sulfate Sodium dodecyl sulfate is the most widely used of the anionic alkyl sulfate surfactants[1]
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Dodecyl azide (1-azidododecane) is an aliphatic organic azide bearing a 12-carbon hydrophobic tail and a reactive terminal azide (N3) group. It is used as a lipophilic clickable handle for copper-catalyzed and strain-promoted azide-alkyne cycloadditions (for example with alkynes, BCN, or DBCO). Molecular formula C12H25N3; molecular weight 211.35 g·mol⁻¹. Store under cold conditions per supplier guidance.
Terminal azide functional group for click chemistry.
12-carbon hydrophobic tail for incorporation into lipophilic environments.
Suitable for copper-catalyzed and strain-promoted azide-alkyne cycloadditions.
High purity as indicated on batch certificate of analysis.
Supplied in laboratory pack sizes for synthesis and labeling workflows.
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Phenelzine sulfate (CAS 156-51-4) is a small-molecule inhibitor of monoamine oxidase (MAO) targeting both MAO-A and MAO-B isoforms By blocking MAO activity phenelzine sulfate limits the enzymatic degradation of monoamine neurotransmitters including norepinephrine serotonin and dopamine resulting in elevated synaptic levels This modulation of neurotransmitter availability underpins its utility in neuropharmacological research on mood regulation neurochemical signaling and mechanistic studies of neurotransmitter dynamics Phenelzine sulfate is commonly utilized to investigate the molecular and cellular effects of altered monoaminergic transmission in neuroscience and psychiatric research models
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GC7 (N1-guanyl-1 7-diaminoheptane) Sulfate is an inhibitor of deoxyhypusine synthase (DHPS) GC7 inhibits Neuroblastoma (NB) cell proliferation in a dose-dependent manner through induction of the cell cycle inhibitor p21 and reduction of total and phosphorylated Rb proteins
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Copper(II) sulfate is an inorganic compound that serves as a source of copper ions. It can form coordination compounds when copper ions coordinate with ligands. This compound is utilized for various enzymatic studies and in material synthesis.
Serves as a source of copper ions
Forms coordination compounds
Utilized for various enzymatic studies
Used in material synthesis
Synthesizes anionic copper sulfate aggregates and chains for magnetic research
Employed as a copper supplement in animal nutrition
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Colistin Sulfate (1264-72-8) is a cyclic antimicrobial peptide targeting the outer membrane of Gram-negative bacteria It is designed to interact electrostatically with negatively charged lipopolysaccharides thereby disrupting membrane integrity and permeability Colistin Sulfate exerts its biological activity primarily through disruption of the bacterial outer membrane In bacterial inhibition assays Colistin Sulfate demonstrates inhibitory activity with IC50 values typically ranging from 0 5 5 g/mL depending on the bacterial strain and experimental conditions Based on these pharmacological properties Colistin Sulfate holds research potential in antimicrobial applications particularly against multidrug-resistant Gram-negative organisms and as a selective agent in bacterial cell culture protocols
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Framycetin sulfate is an aminoglycoside antibiotic that acts as a potent inhibitor of RNase P cleavage activity. It competes for specific divalent metal ion binding sites in RNase P RNA and also inhibits hammerhead ribozyme. This compound is a 5″-azido neomycin B precursor and binds to the Drosha site in miR-525. It is used in the treatment of hepatic encephalopathy and infections caused by enteropathogenic E. coli.
Potent RNase P cleavage activity inhibitor
Inhibits hammerhead ribozyme
Binds to the Drosha site in miR-525
Effective against hepatic encephalopathy and enteropathogenic E. coli infections
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