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 51 to 60 of 67 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

α-Lipoic Acid

1077-28-7sc-202032
sc-202032A
sc-202032B
sc-202032C
sc-202032D
5 g
10 g
250 g
500 g
1 kg
$68.00
$120.00
$208.00
$373.00
$702.00
3
(1)

α-Lipoic Acid serves as a vital coenzyme in mitochondrial energy metabolism, facilitating the decarboxylation of α-keto acids. Its unique ability to function in both aqueous and lipid environments enhances its role in redox reactions, allowing it to regenerate antioxidants like vitamins C and E. The compound's dual solubility promotes efficient electron transfer, while its thiol groups participate in critical enzymatic reactions, influencing metabolic pathways and energy production.

Pentadecanoyl Coenzyme A

24870-39-1sc-479015
1 mg
$430.00
(0)

Pentadecanoyl Coenzyme A functions as a vital coenzyme in fatty acid metabolism, particularly in the elongation and oxidation of long-chain fatty acids. Its unique acyl chain length influences membrane fluidity and protein interactions, enhancing substrate specificity in enzymatic reactions. The compound's ability to form stable thioester bonds allows for efficient transfer of acyl groups, driving critical biochemical pathways and energy production in cellular processes.

Pyridoxal-5′-phosphate monohydrate

41468-25-1sc-202787
sc-202787A
5 g
25 g
$175.00
$310.00
(0)

Pyridoxal-5′-phosphate monohydrate serves as a crucial coenzyme in amino acid metabolism, particularly in transamination and decarboxylation reactions. Its aldehyde group facilitates the formation of Schiff bases with amino acids, enhancing substrate binding and specificity. This coenzyme plays a pivotal role in neurotransmitter synthesis and the metabolism of carbohydrates, influencing reaction kinetics and pathway regulation. Its unique ability to stabilize reaction intermediates contributes to efficient enzymatic activity.

Coenzyme Q9

303-97-9sc-207451A
sc-207451B
sc-207451
sc-207451C
sc-207451D
sc-207451E
500 µg
1 mg
2.5 mg
5 mg
10 mg
25 mg
$194.00
$296.00
$604.00
$1002.00
$1837.00
$4080.00
(1)

Coenzyme Q9 is integral to the electron transport chain, functioning as a vital electron carrier in cellular respiration. Its unique quinone structure allows for reversible redox reactions, facilitating the transfer of electrons between complexes. This coenzyme enhances the efficiency of ATP synthesis by stabilizing the proton gradient across the mitochondrial membrane. Additionally, its hydrophobic nature aids in membrane integration, influencing the dynamics of lipid interactions and overall mitochondrial function.

Thiamine pyrophosphate

154-87-0sc-215966
sc-215966A
sc-215966B
sc-215966C
sc-215966D
1 g
5 g
25 g
100 g
1 kg
$32.00
$95.00
$284.00
$1126.00
$5906.00
1
(1)

Thiamine pyrophosphate serves as a crucial coenzyme in carbohydrate metabolism, particularly in the decarboxylation of alpha-keto acids. Its unique diphosphate structure enables it to form transient covalent bonds with enzyme active sites, enhancing substrate specificity and reaction rates. This coenzyme plays a pivotal role in the pyruvate dehydrogenase complex and the pentose phosphate pathway, facilitating the conversion of substrates into energy-rich molecules while influencing metabolic flux and enzyme kinetics.

Acetyl coenzyme A trisodium salt

102029-73-2sc-210745
sc-210745A
sc-210745B
1 mg
5 mg
1 g
$46.00
$80.00
$5712.00
3
(3)

Acetyl coenzyme A sodium salt acts as a vital coenzyme in various metabolic pathways, particularly in the transfer of acetyl groups. Its unique thioester bond allows for high-energy acetyl transfer, promoting efficient substrate conversion in the citric acid cycle and fatty acid synthesis. This compound also participates in the regulation of metabolic flux, influencing enzyme activity through allosteric interactions and contributing to the dynamic balance of cellular energy production.

Pyridoxal 5′-phosphate

41468-25-1sc-215762
sc-215762A
sc-215762B
sc-215762C
sc-215762D
sc-215762E
1 g
5 g
25 g
100 g
250 g
1 kg
$66.00
$204.00
$663.00
$1948.00
$3682.00
$10210.00
(1)

Pyridoxal 5'-phosphate serves as a crucial coenzyme in amino acid metabolism, facilitating transamination and decarboxylation reactions. Its aldehyde group forms a Schiff base with amino acids, enhancing substrate specificity and reaction rates. This coenzyme is integral in neurotransmitter synthesis and the metabolism of homocysteine, influencing key pathways in cellular signaling. Its role in enzymatic catalysis is characterized by unique interactions that stabilize transition states, optimizing reaction kinetics.

Calcium L-ascorbate dihydrate

5743-28-2sc-257212
100 g
$42.00
(0)

Calcium L-ascorbate dihydrate acts as a vital coenzyme in various biochemical pathways, particularly in collagen synthesis and antioxidant defense. Its unique structure allows for effective electron donation, enhancing redox reactions. The calcium component aids in stabilizing the ascorbate form, promoting its solubility and bioavailability. This coenzyme participates in enzymatic reactions by facilitating the conversion of substrates through specific molecular interactions, ultimately influencing metabolic efficiency and cellular function.

β-Nicotinamide adenine dinucleotide, reduced disodium salt

606-68-8sc-215562
sc-215562A
50 mg
500 mg
$29.00
$91.00
(0)

β-Nicotinamide adenine dinucleotide, reduced disodium salt serves as a crucial coenzyme in cellular metabolism, particularly in redox reactions. Its unique ability to accept and donate electrons facilitates energy transfer within metabolic pathways. The disodium salt form enhances solubility, allowing for efficient interaction with enzymes. This coenzyme plays a pivotal role in dehydrogenase reactions, influencing reaction kinetics and promoting the regeneration of oxidized forms, thereby sustaining cellular energy balance.

Decanoyl coenzyme A monohydrate

1264-57-9sc-214860
sc-214860A
5 mg
25 mg
$160.00
$555.00
(0)

Decanoyl coenzyme A monohydrate is a vital coenzyme involved in fatty acid metabolism and energy production. Its acyl group enables specific interactions with enzymes, facilitating the transfer of acyl groups in various biochemical pathways. This compound participates in the synthesis and degradation of fatty acids, influencing metabolic flux. The monohydrate form enhances stability and solubility, promoting efficient enzyme-substrate interactions and optimizing reaction rates in metabolic processes.