Date published: 2025-12-19

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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 31 to 40 of 67 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Benzoyl coenzyme A lithium salt

102185-37-5sc-214589
5 mg
$372.00
(0)

Benzoyl coenzyme A lithium salt acts as a crucial coenzyme in acylation reactions, playing a significant role in the transfer of acyl groups. Its structure allows for specific interactions with enzymes, enhancing substrate binding and promoting catalytic efficiency. The lithium salt form may alter the solvation dynamics, impacting the reaction environment and influencing the kinetics of acyl transfer. This unique behavior aids in the regulation of metabolic pathways involving fatty acid metabolism and biosynthesis.

Uracil

66-22-8sc-296682
sc-296682A
5 g
25 g
$40.00
$49.00
1
(0)

Uracil serves as a vital coenzyme in various biochemical pathways, particularly in RNA synthesis and nucleotide metabolism. Its unique ability to form hydrogen bonds with complementary bases facilitates the stabilization of nucleic acid structures. Additionally, uracil participates in the regulation of enzymatic activity through its interactions with specific proteins, influencing reaction rates and substrate specificity. This dynamic role underscores its importance in cellular processes and genetic information transfer.

Oleoyl coenzyme A

1716-06-9sc-286621
sc-286621A
5 mg
25 mg
$230.00
$939.00
(0)

Oleoyl coenzyme A is a crucial coenzyme involved in fatty acid metabolism and energy production. It acts as an acyl donor in various enzymatic reactions, facilitating the transfer of acyl groups to substrates. Its unique structure allows for specific interactions with enzymes, enhancing reaction kinetics and substrate affinity. Additionally, oleoyl coenzyme A plays a role in signaling pathways, influencing lipid biosynthesis and cellular energy homeostasis through its dynamic interactions within metabolic networks.

Octanoyl coenzyme A lithium salt

324518-20-9sc-215619
sc-215619A
sc-215619B
5 mg
10 mg
25 mg
$226.00
$393.00
$795.00
1
(0)

Octanoyl coenzyme A lithium salt serves as a vital coenzyme in lipid metabolism, particularly in the synthesis and degradation of fatty acids. Its unique acyl chain length influences enzyme specificity and substrate recognition, promoting efficient acyl transfer reactions. The lithium salt form enhances solubility and stability, facilitating its participation in metabolic pathways. This compound also plays a role in regulating energy balance and metabolic flux through its interactions with various enzymes and cofactors.

Arachidonoyl coenzyme A lithium salt

188174-63-2sc-214551
sc-214551A
5 mg
10 mg
$298.00
$544.00
1
(0)

Arachidonoyl coenzyme A lithium salt is a crucial coenzyme involved in the metabolism of arachidonic acid, influencing signaling pathways and lipid biosynthesis. Its unique structure allows for specific interactions with enzymes, enhancing substrate affinity and catalytic efficiency. The lithium salt form improves solubility, promoting rapid incorporation into metabolic cycles. This compound also modulates cellular responses through its role in the production of bioactive lipids, impacting various physiological processes.

Crotonoyl coenzyme A trilithium salt

102680-35-3sc-300396
sc-300396A
5 mg
25 mg
$442.00
$1509.00
1
(0)

Crotonoyl coenzyme A trilithium salt serves as a pivotal coenzyme in fatty acid metabolism, facilitating the conversion of crotonic acid derivatives. Its trilithium salt form enhances ionic interactions, promoting stability and solubility in aqueous environments. This compound participates in unique enzymatic pathways, accelerating reaction kinetics and influencing acylation processes. By modulating enzyme activity, it plays a significant role in lipid metabolism and energy production.

β-Nicotinamide adenine dinucleotide phosphate

53-59-8sc-215560
sc-215560A
100 mg
250 mg
$114.00
$198.00
(1)

β-Nicotinamide adenine dinucleotide phosphate (NADPH) functions as a crucial coenzyme in various biosynthetic reactions, particularly in the reduction of carbonyl groups. It acts as a powerful electron donor, participating in redox reactions that drive anabolic processes. NADPH is integral to the pentose phosphate pathway, where it aids in generating ribose-5-phosphate and maintaining cellular redox balance. Its unique ability to stabilize transient enzyme-substrate complexes enhances reaction specificity and efficiency.

β-Nicotinamide Adenine Dinucleotide Disodium Salt, reduced form

606-68-8sc-291982B
sc-291982
sc-291982C
sc-291982A
sc-291982D
50 mg
100 mg
500 mg
1 g
5 g
$41.00
$57.00
$127.00
$158.00
$656.00
(0)

β-Nicotinamide adenine dinucleotide disodium salt, reduced form, serves as a vital coenzyme in cellular metabolism, particularly in energy transfer and redox reactions. It facilitates the transfer of electrons in metabolic pathways, enhancing the efficiency of enzymatic reactions. Its unique structure allows for specific interactions with dehydrogenases, promoting substrate binding and stabilization. This coenzyme plays a key role in maintaining cellular homeostasis and regulating metabolic flux.

Riboflavin 5′-Monophosphate Sodium Salt

130-40-5sc-296265
sc-296265A
5 g
25 g
$82.00
$165.00
6
(2)

Riboflavin 5'-Monophosphate Sodium Salt functions as a crucial coenzyme in various biochemical processes, particularly in the metabolism of carbohydrates, fats, and proteins. Its unique phosphate group enhances solubility and reactivity, allowing it to participate in electron transfer and redox reactions. This compound interacts specifically with flavoproteins, influencing enzyme activity and stability, thereby modulating metabolic pathways and energy production within cells.

Folinic acid calcium salt

1492-18-8sc-252837
sc-252837A
100 mg
500 mg
$92.00
$368.00
3
(1)

Folinic acid calcium salt serves as a vital coenzyme in one-carbon metabolism, facilitating the transfer of carbon units in various biochemical reactions. Its unique calcium salt form enhances stability and solubility, promoting efficient interaction with enzymes involved in nucleotide synthesis and amino acid metabolism. This compound plays a key role in modulating enzymatic activity through specific binding interactions, influencing reaction kinetics and metabolic flux in cellular processes.