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Organic compounds that contain a carboxyl group bonded to an organic functional group; carboxyl groups consist of a carbonyl group bonded to a hydroxy group. Includes compounds that are derived from carboxylic acids.
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Azlocillin sodium salt (CAS 37091-65-9) is a small-molecule inhibitor targeting penicillin-binding proteins (PBPs) It is designed to inhibit bacterial cell wall synthesis thereby impeding cross-linking of peptidoglycan layers and inducing bacterial lysis Azlocillin sodium salt exerts its biological activity primarily through inhibition of PBPs disrupting cell wall integrity in bacteria In microbiological assays azlocillin demonstrates broad-spectrum antibacterial activity against both Gram-positive and Gram-negative bacteria reported IC50 values vary by microbial species and experimental conditions typically determined in minimum inhibitory concentration (MIC) assays Based on these pharmacological properties azlocillin sodium salt holds research potential in microbiological and biomedical investigations including studies of bacterial susceptibility resistance mechanisms and combinational antimicrobial therapies
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Rp-cAMPS sodium salt is a cAMP analog and competitive antagonist of cAMP-dependent protein kinase A (PKA I/II), used to inhibit PKA signaling in biochemical and cellular assays.
Acts as a cAMP analog and competitive PKA antagonist.
High purity: 99.69%.
Molecular formula C10H11N5NaO5PS; molecular weight 367.25.
White to pink solid; soluble in water and DMSO.
Available in small research quantities including 50 mg.
Store sealed, away from moisture and light; in solvent: -80°C (6 months), -20°C (1 month).
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Acetazolamide (CAS 59-66-5) is a small-molecule inhibitor targeting carbonic anhydrase (CA) It is designed to inhibit CA activity thereby modulating neuronal ion flux and influencing neurotransmission Acetazolamide exerts its biological activity primarily through inhibition of carbonic anhydrase an enzyme catalyzing the reversible hydration of carbon dioxide In experimental studies acetazolamide demonstrates potent inhibition with reported IC50 values for various CA isoforms typically ranging from 5 to 30 nM depending on isoenzyme subtype and assay conditions Based on these pharmacological properties acetazolamide holds research potential in studies of neuronal excitability synaptic transmission and seizure pathophysiology including models of absence tonic-clonic myoclonic and atonic seizures
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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<|a>
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More