Acyl-CoA & Cofactors

Cat. No.

A91077

CAS No.

1245946-43-3

3-(4-Methylpent-3-en-1-yl)pent-2-enedioyl-CoA

Synonyms: 3-(4-Methylpent-3-en-1-yl)pent-2-enedioyl-coenzyme A

3-(4-Methylpent-3-en-1-yl)pent-2-enedioyl-CoA is a coenzyme A derivative that plays a crucial role as a substrate in biochemical pathways involving fatty acid metabolism. This 2-enoyl-CoA compound is valuable for studying various enzymatic reactions and lipid biosynthesis mechanisms. Its applications extend to metabolic research and the investigation of regulatory processes in cellular environments.

Cat. No.

A91107

CAS No.

148407-07-2

UDP-galacturonic acid trisodium

UDP-galacturonic acid trisodium is a cofactor crucial for various biochemical reactions, particularly serving as a substrate for UDP-glucose dehydrogenase. This compound plays a significant role in the synthesis and metabolism of pectin and other polysaccharides. Its unique structure enables participation in glycosylation processes and cell wall formation, making it valuable in research related to plant biology and carbohydrate chemistry.

Cat. No.

A91128

CAS No.

124924-91-0

2-Tolylacetyl-CoA

Synonyms: 2-Tolylacetyl-coenzyme A

2-Tolylacetyl-CoA is a coenzyme A derivative that serves as an important substrate in various biochemical pathways. This compound is utilized in research focused on fatty acid metabolism and the biosynthesis of aromatic compounds. Its ability to facilitate acyl group transfers makes it a valuable tool for studies in enzymology and metabolic engineering.

Cat. No.

A91148

CAS No.

852100-90-4

Pentacosanoyl-CoA

Pentacosanoyl-CoA is a fatty acyl-CoA compound that serves as a substrate for the enzyme AGPAT11. This reagent plays a crucial role in lipid metabolism and is essential for the biosynthesis of glycerolipids. Its applications extend to various research areas, including studies on fatty acid metabolism and an investigation of lipid-related disorders.

Cat. No.

A91217

CAS No.

1245946-53-5

5-Methyl-3-oxo-4-hexenoyl-CoA

Synonyms: 5-Methyl-3-oxo-4-hexenoyl-coenzyme A

5-Methyl-3-oxo-4-hexenoyl-CoA is a coenzyme A derivative that acts as an acyl-CoA substrate in metabolic pathways. This compound plays a key role in fatty acid metabolism and has potential applications in studying lipid biosynthesis and energy production. Research involving 5-Methyl-3-oxo-4-hexenoyl-CoA can provide insights into metabolic regulation and the biochemical mechanisms underlying various physiological processes.

Cat. No.

A91225

CAS No.

56898-43-2

(Methylenecyclopropyl)acetyl-CoA

Synonyms: S-(2-Methylenecyclopropyl)acetyl-CoA

(Methylenecyclopropyl)acetyl-CoA is a coenzyme A derivative that serves as a substrate in various metabolic pathways. It is involved in the transfer of acyl groups and has potential applications in research focused on metabolic regulation and enzyme activity. This compound can be utilized to study the mechanistic aspects of acylation reactions and the role of CoA in cellular metabolism.

Cat. No.

A91272

CAS No.

4460-95-1

2E-Hexadecenoyl-CoA

Synonyms: 2E-Hexadecenoyl-coenzyme A; trans-2-Hexadecenoyl-CoA; trans-2-Hexadecenoyl-S-coenzyme A

2E-Hexadecenoyl-CoA is a 2-enoyl-CoA derivative and a long-chain fatty acyl-CoA that serves as a key substrate in fatty acid metabolism. It is involved in various biochemical pathways, including fatty acid β-oxidation and lipid synthesis. This compound is essential for studying metabolic processes and investigating the role of fatty acids in cellular functions and energy homeostasis.

Cat. No.

A91276

CAS No.

72845-19-3

Citryl-Thioether-CoA

Synonyms: Citryl-Thioether-Coenzyme A

Citryl-Thioether-CoA is a coenzyme A derivative that serves as a substrate for various enzymatic reactions involved in cellular metabolism. This compound exhibits critical biological activity, particularly in the synthesis of thiol esters and in metabolic pathways associated with energy production and biosynthesis. It is particularly applicable in studies of metabolic regulation and enzyme kinetics involving coenzyme A-related processes.

Cat. No.

A91433

CAS No.

155147-45-8

Tridecanedioyl-CoA

Synonyms: Tridecanedioyl-coenzyme A

Tridecanedioyl-CoA is a coenzyme A derivative that serves as a crucial substrate in fatty acid metabolism. This compound is involved in the activation and elongation of long-chain fatty acids, facilitating their incorporation into lipid biosynthesis pathways. Its application is particularly relevant in studies focused on metabolic disorders, energy metabolism, and the regulation of cellular lipid composition.

Cat. No.

A91522

CAS No.

149542-22-3

2-Fluorooctanoyl-CoA

Synonyms: 2-Fluorooctanoyl-coenzyme A

2-Fluorooctanoyl-CoA is a coenzyme A derivative that serves as a substrate for various acyltransferase enzymes in metabolic pathways. This compound is primarily utilized in studies investigating fatty acid metabolism and lipid biosynthesis. Its role in cellular processes makes it valuable for research into metabolic disorders and bioenergetics.

Cat. No.

A91634

CAS No.

799812-89-8

Oleoyl Coenzyme A triammonium

Oleoyl Coenzyme A triammonium is the ammonium salt of Oleoyl Coenzyme A, primarily functioning as a substrate in metabolic processes. It exhibits inhibitory effects on neutral lipase, which is significant in lipid metabolism. This compound is essential for studying ATP-dependent signal transduction pathways in plants and can be employed in various biological research applications related to fatty acid metabolism and regulation.

Cat. No.

A91670

CAS No.

799812-81-0

Hexanoyl-coenzyme A triammonium

Synonyms: 06:0 Coenzyme A triammonium

Hexanoyl-Coenzyme A triammonium is a medium-chain fatty acyl CoA that serves as an acyl donor substrate for the enzyme ghrelin O-acyltransferase (GOAT). Its primary mechanism involves the acylation of ghrelin, which plays a critical role in regulating energy homeostasis and appetite. This compound is valuable in metabolic research and studies examining the role of ghrelin acylation in physiological processes and disorders related to energy balance.

Cat. No.

A91717

CAS No.

87935-97-5

Myristoleoyl-CoA

Synonyms: Coenzyme A,S-(9Z)-9-tetradecenoate

Myristoleoyl-CoA is a coenzyme A derivative that serves as a critical substrate in lipid metabolism. This compound is involved in the biosynthesis of fatty acids and can influence metabolic pathways related to energy production and cellular signaling. Myristoleoyl-CoA is valuable for research applications focusing on lipid biochemistry, metabolic disorders, and enzymatic reactions related to fatty acid synthesis.

Cat. No.

A91885

CAS No.

97919-43-2

S-[3-(Acetylthio)propanoate]-CoA

Synonyms: S-[3-(Acetylthio)propanoate]-coenzyme A

S-[3-(Acetylthio)propanoate]-CoA is a coenzyme A derivative that serves as a key biochemical substrate in various metabolic pathways. Its primary mechanism involves participation in acylation reactions, facilitating the transfer of acyl groups. This compound is invaluable for studies in lipid metabolism, enzymatic activity, and the regulation of cellular processes related to energy production and biosynthesis.

Cat. No.

A92001

CAS No.

53501-94-3

Methyl coenzyme M ammonium

Methyl coenzyme M ammonium serves as a crucial substrate for methyl-coenzyme M reductase, facilitating the reversible synthesis of methane in methanogenic archaea, including ANME-1 and ANME-2. This compound is integral for studying the biochemical pathways of methanogenesis and the role of archaea in carbon cycling. Its applications extend to environmental microbiology and bioenergy research, providing insights into microbial metabolism and methane production processes.

Cat. No.

A92086

CAS No.

86029-72-3

VP-CoA

Synonyms: VP-Coenzyme A; Valproyl-CoA; Valproyl-coenzyme A

VP-CoA is a coenzyme A derivative that serves as a crucial substrate for various enzymatic reactions. It plays a significant role in metabolic pathways, particularly in the activation and metabolism of fatty acids and amino acids. VP-CoA is valuable for studies focusing on energy metabolism, lipid biosynthesis, and cellular signaling. Researchers can utilize this reagent to explore its effects in biochemical assays and metabolic studies.

Cat. No.

A92218

CAS No.

52530-01-5

Cyclopropanecarboxyl-CoA

Synonyms: S-cyclopropanecarboxyl-coenzyme A

Cyclopropanecarboxyl-CoA is a coenzyme A derivative that serves as a substrate in various biochemical reactions. It plays a crucial role in metabolic pathways related to fatty acid metabolism and amino acid synthesis. This compound is valuable for research applications focused on enzyme assays and metabolic flux analysis.

Cat. No.

A92467

CAS No.

70019-68-0

S-Ethyl-CoA

Synonyms: S-Ethylcoenzyme A

S-Ethyl-CoA is a derivative of coenzyme A that serves as an important substrate in various biochemical pathways. It plays a crucial role in the metabolism of fatty acids and participates in the synthesis of acetyl-CoA. This compound is utilized in research applications focused on metabolic studies, enzymatic reactions, and the investigation of coenzyme A-related processes.

Cat. No.

A92652

CAS No.

40780-14-1

Linolenoyl-CoA

Synonyms: Linolenoyl coenzyme A

Linolenoyl-CoA is a coenzyme A derivative that serves as a pivotal substrate in fatty acid metabolism. It plays a crucial role in the biosynthesis of polyunsaturated fatty acids and is involved in lipid signaling pathways. Linolenoyl-CoA is valuable for research applications in biochemistry and molecular biology, particularly in studies investigating lipid metabolism and cellular energy regulation.

Cat. No.

A92733

CAS No.

61083-44-1

(2E,9Z)-Octadecadienoyl-CoA

Synonyms: (2E,9Z)-Octadecadienoyl-coenzyme A

(2E,9Z)-Octadecadienoyl-CoA is a polyunsaturated fatty acyl-CoA derivative that serves as a substrate for various enzymatic reactions. It plays a significant role in lipid metabolism, particularly in the synthesis and degradation of fatty acids. This compound is valuable for research applications related to metabolic pathways and lipid signaling.

Cat. No.

A92736

CAS No.

96448-59-8

2-Octynoyl-CoA

2-Octynoyl-CoA is a coenzyme A derivative that serves as an important substrate in fatty acid metabolism and biosynthesis. Its unique structure allows for the study of acyl-CoA metabolism and its role in various biochemical pathways. This compound is utilized in research exploring lipid biochemistry, metabolic regulation, and enzymatic activity in relation to acyl-CoA derivatives.

Cat. No.

A92810

CAS No.

279256-67-6

Ac-Lys(CoA)-NH2

Synonyms: Ac-Lys(coenzyme A)-NH2

Ac-Lys(CoA)-NH2 is a coenzyme A derivative that serves as a versatile substrate in various biochemical reactions. This compound plays a crucial role in enzymatic processes involving acyl group transfers and is instrumental in studies related to metabolism and cellular respiration. Its application extends to research investigating the mechanisms of acylation and the role of coenzyme A in metabolic pathways.

Cat. No.

A92875

CAS No.

138149-22-1

trans-2-Dodecenedioyl-CoA

Synonyms: trans-2-Dodecenedioyl-coenzyme A

trans-2-Dodecenedioyl-CoA is a coenzyme A derivative that functions as an essential acyl-CoA substrate. This compound is involved in various metabolic pathways, including fatty acid metabolism and synthesis. It serves as a vital tool for studying acyl-CoA biosynthesis and regulation in biochemical research and can facilitate investigations into metabolic disorders.

Cat. No.

A92926

CAS No.

93255-33-5

PDCoA

Synonyms: Coenzyme A,S-1-pyrenedodecanoate

PDCoA (Coenzyme A, S-1-pyrenedodecanoate) is a coenzyme A derivative that serves as a key substrate for various metabolic pathways. This compound is utilized in research focused on lipid metabolism and enzyme activity modulation. Its structural features enable the investigation of CoA-dependent biological processes and the characterization of enzyme-substrate interactions.

Cat. No.

A92938

CAS No.

359868-77-2

5-Oxo-furan-2-acetyl-CoA

Synonyms: 5-Oxo-furan-2-acetyl-coenzyme A

5-Oxo-furan-2-acetyl-CoA is a coenzyme A derivative that functions as a substrate in various metabolic pathways. This compound is involved in the acetylation of various substrates, thereby playing a crucial role in cellular metabolism. Its utility extends to research applications focused on metabolic regulation and enzymatic activity pertaining to coenzyme A derivatives.