Quinolines and derivatives
Abcam Quinine hemisulfate monohydrate, Potassium channel blocker, 25G
MW 391.47 g/mol. Potassium channel blocker. Antimalarial, anticholinergic, antihypertensive and hypoglycemic agent. Inhibits mitochondrial ATP-regulated potassium channel. Also used to study the metabolism of biocrystalized heme, hemozoin, in malarial parasites and to study the toxicity of heme (FP)-complexes.
The product is subject to the following: Abcam Restricted Use Statement
Apexbio Technology LLC Penicillin V potassium salt 132-98-9 200mg
Penicillin V potassium salt (132-98-9) is a small-molecule inhibitor targeting bacterial cell wall peptidoglycan synthesis It is designed to inhibit this biosynthetic pathway thereby suppressing the growth of Gram-positive bacteria Penicillin V potassium salt exerts its biological activity primarily through inhibition of bacterial cell wall synthesis In microbial susceptibility assays Penicillin V potassium salt demonstrates inhibitory effects with IC50 values ranging from approximately 0 01 to 0 5 g/mL for sensitive bacterial strains Based on these pharmacological properties Penicillin V potassium salt holds research potential in studies investigating Gram-positive bacterial resistance mechanisms cell-wall targeting antibiotic actions and experimental models of upper respiratory tract infections including otitis media sinusitis pharyngitis and tonsillitis
Medchemexpress LLC Sulfo-cyanine3 azide (potassium) | 1658416-54-6 | 95.3% | 10 MG
Sulfo-cyanine3 azide (potassium) is a water-soluble, sulfonated cyanine fluorescent azide for bioorthogonal labeling via azide-alkyne click chemistry. It exhibits Cy3-like optical properties with excitation/emission near 548/563 nm, and is supplied as a potassium salt with a certificate of analysis for documented purity.
- Cy3-like excitation/emission (548/563 nm).
- Water-soluble sulfonated dye for aqueous labeling.
- Reactive azide group for azide-alkyne click chemistry.
- Supplied as a potassium salt with certificate of analysis and documented purity.
- Suitable for labeling proteins, peptides, and oligonucleotides.
Selleck Chemical LLC Quinidine hydrochloride monohydrate S4681-1g
Quinidine hydrochloride monohydrate is an anti-arrythmic agent and a potent potassium channel inhibitor with IC50 of 19 9 M
Selleck Chemical LLC Quinidine hydrochloride monohydrate S4681-25mg
Quinidine hydrochloride monohydrate is an anti-arrythmic agent and a potent potassium channel inhibitor with IC50 of 19 9 M
Selleck Chemical LLC Quinine S4495-25mg
Quinine an alkaloid derived from the bark of the cinchona tree is an anti-malaria agent and a potassium channel inhibitor that inhibits mSlo3 (KCa 5 1) channel currents evoked by voltage pulses to 100 mV with IC50 of 169 M
Apexbio Technology LLC Quinidine 56-54-2 50mg
Quinidine (CAS 56-54-2) is a small-molecule inhibitor targeting sodium (Na ) and potassium (K ) ion channels It is designed to inhibit these ion channel currents thereby modulating cardiac electrophysiological processes Quinidine exerts its biological activity primarily through inhibition of Na and K currents In in vitro studies quinidine demonstrates inhibitory activity with an IC50 of approximately 41 M on the transient outward potassium current (Ik) at a membrane potential of 0 mV Based on these pharmacological properties quinidine holds research potential in the fields of cardiac electrophysiology ion channel pharmacology drug metabolism and drug-drug interaction mechanisms
Apexbio Technology LLC Quinidine 56-54-2 10mM (in 1mL DMSO)
Quinidine (CAS 56-54-2) is a small-molecule inhibitor targeting sodium (Na ) and potassium (K ) ion channels It is designed to inhibit these ion channel currents thereby modulating cardiac electrophysiological processes Quinidine exerts its biological activity primarily through inhibition of Na and K currents In in vitro studies quinidine demonstrates inhibitory activity with an IC50 of approximately 41 M on the transient outward potassium current (Ik) at a membrane potential of 0 mV Based on these pharmacological properties quinidine holds research potential in the fields of cardiac electrophysiology ion channel pharmacology drug metabolism and drug-drug interaction mechanisms