Items 21 to 30 of 67 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
β-Methylcrotonyl coenzyme A lithium salt | 108347-83-7 | sc-215380 sc-215380A | 10 mg 25 mg | $377.00 $822.00 | ||
β-Methylcrotonyl coenzyme A lithium salt serves as a key coenzyme in metabolic processes, particularly in the catabolism of branched-chain amino acids. Its lithium salt form contributes to increased ionic strength, facilitating enzyme-substrate binding. The compound's unique structural features enable it to stabilize transition states during enzymatic reactions, enhancing reaction rates. Additionally, it plays a role in the regulation of metabolic flux, influencing energy production pathways. | ||||||
Pyridoxal, Hydrochloride | 65-22-5 | sc-205826 | 25 g | $213.00 | ||
Pyridoxal hydrochloride acts as a vital coenzyme in amino acid metabolism, particularly in transamination and decarboxylation reactions. Its aldehyde group participates in the formation of Schiff bases with amino acids, promoting efficient substrate conversion. The compound's ability to stabilize reactive intermediates enhances enzymatic activity, while its interactions with various enzymes facilitate the modulation of metabolic pathways, ensuring proper nutrient utilization and energy balance. | ||||||
Calcium D-(+)-pantothenate | 137-08-6 | sc-202515 sc-202515A | 10 g 100 g | $36.00 $74.00 | 1 | |
Calcium D-(+)-pantothenate serves as a crucial coenzyme in the synthesis of coenzyme A, integral to fatty acid metabolism and the Krebs cycle. Its unique structure allows for effective binding with acyl groups, facilitating the transfer of acyl moieties in metabolic reactions. The compound enhances enzyme kinetics by stabilizing transition states, thereby accelerating the conversion of substrates. Its role in energy production and biosynthetic pathways underscores its importance in cellular metabolism. | ||||||
Octanoyl coenzyme A | 1264-52-4 | sc-286614 sc-286614A | 5 mg 25 mg | $510.00 $1430.00 | ||
Octanoyl coenzyme A is a pivotal coenzyme involved in fatty acid metabolism, particularly in the elongation and degradation of fatty acids. Its acyl group facilitates specific interactions with enzymes, promoting the transfer of acyl chains in various biochemical pathways. The compound exhibits unique kinetic properties, enhancing the efficiency of enzymatic reactions by lowering activation energy barriers. Its structural configuration allows for versatile binding, influencing metabolic flux and energy homeostasis within cells. | ||||||
Mecobalamin | 13422-55-4 | sc-211781 | 10 mg | $300.00 | ||
Mecobalamin, a coenzyme form of vitamin B12, is integral in the synthesis of methionine from homocysteine, a key step in the methylation cycle. Its cobalt ion facilitates the transfer of methyl groups, influencing various metabolic pathways. The compound exhibits unique binding interactions with enzymes, enhancing reaction specificity and efficiency. Additionally, its solubility in water allows for effective cellular uptake, promoting its role in cellular metabolism and energy production. | ||||||
Coenzyme B12 | 13870-90-1 | sc-214754 sc-214754A sc-214754B sc-214754C sc-214754D | 10 mg 25 mg 100 mg 1 g 10 g | $49.00 $75.00 $146.00 $923.00 $4083.00 | 1 | |
Coenzyme B12, a vital cofactor in enzymatic reactions, plays a crucial role in the conversion of methylmalonyl-CoA to succinyl-CoA, a key step in fatty acid metabolism. Its cobalt center enables unique coordination with enzyme active sites, enhancing catalytic efficiency. The compound's ability to stabilize radical intermediates contributes to its effectiveness in metabolic pathways. Furthermore, its structural flexibility allows for diverse interactions, facilitating various biochemical processes. | ||||||
Tetrahydrobiopterin (THB) dihydrochloride | 69056-38-8 | sc-200345 sc-200345A | 25 mg 100 mg | $81.00 $200.00 | 10 | |
Tetrahydrobiopterin (THB) dihydrochloride serves as a critical coenzyme in the biosynthesis of neurotransmitters and nitric oxide. Its unique pteridine structure allows for effective electron transfer and stabilization of reaction intermediates. THB participates in hydroxylation reactions, enhancing substrate specificity and reaction rates. The compound's ability to form hydrogen bonds with enzymes promotes precise molecular recognition, facilitating efficient catalytic processes in various metabolic pathways. | ||||||
NADP, Disodium Salt | 24292-60-2 | sc-205763 sc-205763A sc-205763B | 100 mg 250 mg 1 g | $76.00 $117.00 $316.00 | ||
NADP, Disodium Salt functions as a vital coenzyme in redox reactions, particularly in photosynthesis and anabolic pathways. Its unique nicotinamide structure enables it to accept and donate electrons, influencing reaction kinetics. The compound's phosphate groups enhance solubility and facilitate interactions with enzymes, promoting efficient substrate binding. Additionally, NADP's role in the regeneration of reduced forms of coenzymes underscores its importance in maintaining cellular energy balance and metabolic flux. | ||||||
Coenzyme A sodium salt | 55672-92-9 | sc-214753 sc-214753A | 10 mg 25 mg | $88.00 $145.00 | 1 | |
Coenzyme A sodium salt plays a crucial role in acyl group transfer reactions, acting as a carrier for various acyl moieties in metabolic pathways. Its unique thiol group allows for the formation of thioester bonds, which are key in energy metabolism and fatty acid synthesis. The compound's high reactivity and ability to form stable complexes with acyl groups enhance its efficiency in enzymatic reactions, facilitating the conversion of substrates into energy-rich molecules. | ||||||
NAD+, Lithium Salt | 64417-72-7 | sc-208085 | 1 g | $267.00 | ||
NAD+ lithium salt serves as a vital coenzyme in redox reactions, participating in electron transfer processes essential for cellular respiration. Its unique ability to oscillate between oxidized and reduced states enables it to facilitate the conversion of substrates, enhancing reaction kinetics. The lithium salt form may influence solubility and stability, potentially affecting its interaction with enzymes and substrates, thereby optimizing metabolic pathways and energy production. | ||||||