Date published: 2025-11-24

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Coenzymes

Santa Cruz Biotechnology now offers a broad range of coenzymes for use in various applications. Coenzymes, which are non-protein organic molecules that bind to enzymes, play a crucial role in facilitating enzymatic reactions by acting as carriers of electrons, atoms, or functional groups. These molecules are indispensable in a wide array of biochemical processes, making them vital to scientific research. In the study of metabolic pathways, coenzymes such as NADH, FAD, and CoA are essential for understanding the mechanisms of cellular respiration, photosynthesis, and fatty acid synthesis. Researchers utilize coenzymes to probe the dynamics of enzyme catalysis and to study the structural and functional aspects of enzyme-coenzyme interactions. In molecular biology, coenzymes are instrumental in studying gene expression and regulation, as they participate in processes like DNA replication and repair, RNA transcription, and protein synthesis. Environmental scientists employ coenzymes to investigate microbial metabolism and biogeochemical cycles, which are critical for understanding nutrient cycling and ecosystem functioning. Additionally, coenzymes are used in synthetic biology and biotechnology to engineer metabolic pathways for the production of biofuels and other valuable biochemicals. Analytical chemists rely on coenzymes as reagents and standards in various assays and analytical techniques, enhancing the accuracy and reliability of biochemical measurements. By offering a diverse selection of coenzymes, Santa Cruz Biotechnology supports a wide range of scientific endeavors, enabling researchers to select the appropriate coenzyme for their specific experimental needs. This extensive range of coenzymes facilitates innovation and discovery across multiple scientific disciplines, including biochemistry, molecular biology, environmental science, and biotechnology. View detailed information on our available coenzymes by clicking on the product name.

Items 21 to 30 of 67 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

β-Methylcrotonyl coenzyme A lithium salt

108347-83-7sc-215380
sc-215380A
10 mg
25 mg
$377.00
$822.00
(0)

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

65-22-5sc-205826
25 g
$213.00
(0)

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

137-08-6sc-202515
sc-202515A
10 g
100 g
$36.00
$74.00
1
(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

1264-52-4sc-286614
sc-286614A
5 mg
25 mg
$510.00
$1430.00
(0)

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

13422-55-4sc-211781
10 mg
$300.00
(0)

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

13870-90-1sc-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
(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

69056-38-8sc-200345
sc-200345A
25 mg
100 mg
$81.00
$200.00
10
(1)

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

24292-60-2sc-205763
sc-205763A
sc-205763B
100 mg
250 mg
1 g
$76.00
$117.00
$316.00
(1)

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

55672-92-9sc-214753
sc-214753A
10 mg
25 mg
$88.00
$145.00
1
(0)

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

64417-72-7sc-208085
1 g
$267.00
(0)

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.