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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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NADH disodium salt is an orally active reduced coenzyme. It acts as a donor of ADP-ribose units in ADP-ribosylation reactions and a precursor of cyclic ADP-ribose. This compound functions as a regenerative electron donor in cellular energy metabolism, participating in processes such as glycolysis, β-oxidation, and the tricarboxylic acid (TCA) cycle.
Orally active reduced coenzyme
Donor of ADP-ribose units
Precursor of cyclic ADP-ribose
Plays a role as a regenerative electron donor in cellular energy metabolism, including glycolysis, β-oxidation and the tricarboxylic acid (TCA) cycle
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Cefoxitin sodium salt (CAS 33564-30-6) is a small-molecule inhibitor targeting penicillin-binding proteins (PBPs) It is designed to inhibit PBPs thereby interfering with bacterial cell wall synthesis and peptidoglycan cross-linking Cefoxitin sodium salt exerts its biological activity primarily through inhibition of cell wall synthesis by binding to PBPs In in vitro enzymatic assays Cefoxitin sodium salt demonstrates inhibitory activity against various gram-positive and gram-negative bacteria with previously reported IC50 values in the low micromolar range due to its resistance to certain beta-lactamases including AmpC -lactamases Based on these pharmacological properties Cefoxitin sodium salt holds research potential in investigations of bacterial resistance mechanisms antimicrobial sensitivity profiling and beta-lactamase enzyme kinetics
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DG013B formate is an epimeric phosphinic acid tripeptide-mimetic compound with weak affinity for ERAP1 and ERAP2. It is commonly used as a negative control in biochemical and binding studies involving aminopeptidases and related analogues.
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Medchemexpress, HY-D0850 5g Tartaric acid (disodium dihydrate) CAS:6106-24-7 Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Velnacrine maleate (HP 029) is an orally active cholinesterase inhibitor used in the research of Alzheimer's disease. It is a solid appearing from light yellow to khaki color, and it is soluble in DMSO. This compound is provided with comprehensive data including a datasheet, COA, and SDS.
Orally active cholinesterase inhibitor
Can be used for Alzheimer's disease research
Comprehensive documentation including datasheet, COA, and SDS
Provided as a solid with color ranging from light yellow to khaki
Soluble in DMSO
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NB-598 Maleate is a small-molecule inhibitor targeting squalene epoxidase (SE) an essential enzyme in cholesterol biosynthesis It is designed to inhibit SE thereby disrupting the oxygenation of squalene and affecting downstream synthesis of cholesterol intermediates particularly within farnesol-dependent pathways leading to triglyceride biosynthesis NB-598 Maleate exerts its biological activity primarily through inhibition of squalene epoxidase In mouse pancreatic islet models NB-598 Maleate reduces insulin secretion under both basal and glucose-stimulated conditions Additionally this compound inhibits calcium voltage-dependent (CaV) ion channels in cellular assays Based on these pharmacological properties NB-598 Maleate holds research potential in studying cholesterol biosynthesis pathways lipid metabolism insulin regulation and the physiological role of CaV channels
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