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| Product | Description | |
|---|---|---|
| Coenzyme A Lithium Salt | Supplement. CAS No. 18439-24-2. |  US, Austria, Lithuania |
| 2-Butenoyl coenzyme A lithium salt | 2-Butenoyl coenzyme A lithium salt. CAS No: 102680-35-3 |  Sarchem Laboratories New Jersey NJ |
| 2-Butenoyl coenzyme A lithium salt | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Acetoacetyl coenzyme A-[13C4] lithium salt hydrate | Acetoacetyl coenzyme A-[13C4] lithium salt hydrate is the carbon-13 labelled edition of Acetoacetyl-CoA. Acetoacetyl-CoA is also a precursor of poly-β-hydroxybutyrate polymers in microorganisms. Synonyms: Acetoacetyl-13C4 coenzyme A lithium salt hydrate. Grades: 95% (CP); 99% atom 13C. Molecular formula: C21[13C]4H40N7O18P3S. Mole weight: 855.58 (free acid). |  |
| Acetoacetyl coenzyme A lithium salt | Acetoacetyl coenzyme A lithium salt, a paramount compound employed in the biomedical sector for diverse applications, exhibits immense potential for the management of metabolic disorders and confers therapeutic benefits against ailments like Alzheimer's, Parkinson's, and certain cancers. This indispensably contributes to biochemical pathways by expediting pivotal reactions and augmenting holistic cellular well-being. Grades: 96%. Molecular formula: C25H36N7O18P3SLi4·5H2O. Mole weight: 965.42. | |
| Acetyl coenzyme A lithium salt | ?93% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Acetyl coenzyme A lithium salt | Acetyl coenzyme A lithium salt. Group: Biochemicals. Alternative Names: Acetyl-CoA Li. Grades: Highly Purified. CAS No. 32140-51-5. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H38N7O17P3S·xLi. US Biological Life Sciences. |  Worldwide |
| Acetyl coenzyme A lithium salt | Acetyl coenzyme A trilithium salt is a lithium salt of an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Acetyl coenzyme A is formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degradation of certain amino acids. Acetyl coenzyme A is a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Acetyl-coA is a positive regulator of pyruvate carboxylase and is a precursor of the neurotransmitter acetylcholine. Applications: A cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Group: Coenzymes. Synonyms: Acetyl-S-CoA Li3. CAS No. 32140-51-5. Purity: ≥95%. Mole weight: 881. Appearance: Powder. Form: Solid. Acetyl-S-CoA Li3; Acetyl coenzyme A lithium salt; 32140-51-5. Cat No: COEC-082. |  |
| Acetyl Coenzyme A Lithium Salt | Acetyl Coenzyme A Lithium Salt is an important molecule in enzymatic acetyl transfer reactions. It is the source of the phosphopantetheine group that is added as a prosthetic group to acyl carrier proteins and formyltetrahydrofolate dehydrogenase. Synonyms: Lithium acetyl-CoA; Coenzyme A, S-acetate, lithium salt. Grades: ≥95%. CAS No. 32140-51-5. Molecular formula: C23H38N7O17P3S xLi. Mole weight: 809.58. | |
| Arachidonoyl coenzyme A lithium salt | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| Arachidonoyl coenzyme A lithium salt | Arachidonoyl coenzyme A lithium salt is a substrate for the long-chain N-acylation of glycines by enzymes such as glycine N-acyltransferase-like 2 (GLYATL2) and of acytransferases such as lysophosphatidic acid acyltransferase (CGI-58/ABHD5). Arachidonoyl CoA is used as a charged membrane-impermeant analog of arachidonic acid (AA). Arachidonoyl CoA is used in the synthesis of arachidonoyl amino acids by cytochrome c. Applications: A substrate for the long-chain n-acylation of glycines by enzymes such as glyatl2. Group: Coenzymes. Synonyms: cis,cis,cis,cis-5,8,11,14-Eicosatetraenoyl coenzyme A lithium salt. CAS No. 188174-63-2. Purity: ≥85%. Mole weight: 1059.92. Appearance: Powder. Form: Solid. cis,cis,cis,cis-5,8,11,14-Eicosatetraenoyl coenzyme A lithium salt; Arachidonoyl coenzyme A lithium salt; 188174-63-2. Cat No: COEC-030. | |
| Benzoyl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Benzoyl coenzyme A lithium salt | Benzoyl CoA may be used as a substrate for characterization of specific alcohol acyltransferase characterization and as a substrate for biphenyl synthesis. Applications: A component of benzoyl-coenzyme a. Group: Coenzymes. Synonyms: Benzoyl CoA lithium salt. CAS No. 102185-37-5. Mole weight: 878.58. Form: Solid. Benzoyl CoA lithium salt; Benzoyl coenzyme A lithium salt; 102185-37-5. Cat No: COEC-026. | |
| Benzoyl coenzyme A lithium salt | Benzoyl coenzyme A lithium salt. CAS No: 102185-37-5 | Sarchem Laboratories New Jersey NJ |
| b-Methylcrotonyl coenzyme A lithium salt | b-Methylcrotonyl coenzyme A lithium salt, a crucial compound in the biomedicine realm, boasts paramount importance. Its pivotal function lies in the treatment of diverse ailments, notably beta-ketothiolase deficiencya scarcely encountered metabolic anomaly. Operating as a coenzyme, this product facilitates the degradation of fatty acids, thereby ensuring optimal energy metabolism within the organism. Synonyms: (c5:1)Coenzyme a lithium salt; trans-3-Methyl-2-butenoyl Coenzyme A; lithium [ (2R, 3S, 4R, 5R) -5- (6-aminopurin-9-yl) -4-hydroxy-2- [ [hydroxy- [hydroxy- [3-hydroxy-2, 2-dimethyl-4- [ [3- [2- (3-methylbut-2-enoylsulfanyl) ethylamino] -3-oxopropyl] amino] -4-oxobutoxy] phosphoryl] oxyphosphoryl] oxymethyl] oxolan-3-yl] hydrogen phosphate. Grades: ≥ 95%. CAS No. 108347-83-7. Molecular formula: C26H41LiN7O17P3S. Mole weight: 855.57. | |
| Butyryl coenzyme A lithium salt hydrate | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Coenzyme A, oxidized lithium salt | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| DL-?-Hydroxybutyryl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Glutaryl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Glutaryl coenzyme A lithium salt | Glutaryl coenzyme A is an intermediate in the metabolism (catabolism) of the amino acids lysine and tryptophan. Glutaryl CoA is used as a substrate to study the specificity and kinetics of glutaryl-CoA dehydrogenases. Applications: An intermediate in the metabolism (catabolism) of the amino acids lysine and tryptophan. Group: Coenzymes. Synonyms: Glutaryl CoA. CAS No. 103192-48-9. Purity: ≥90%. Mole weight: 881.63. Appearance: Powder. Form: Solid. Glutaryl CoA; Glutaryl coenzyme A lithium salt; 103192-48-9. Cat No: COEC-053. | |
| Isobutyryl coenzyme A lithium salt | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| Isobutyryl coenzyme A lithium salt | Isobutyryl coenzyme A lithium salt is an acyl group carrier. Isobutyryl coenzyme A (IB-CoA), a short-chain branched acyl-CoA, provides the starter unit for biosynthesis of myxalamid B. Isobutyryl coenzyme A is used as a substrate to study the specificity and kinetics of isobutyryl-coenzyme A (CoA) mutase. Applications: An acyl group carrier. Group: Coenzymes. Synonyms: IB-CoA. CAS No. 103404-95-1. Purity: ≥85%. Mole weight: 837.62 (free acid basis). Appearance: Powder. Form: Solid. IB-CoA; Isobutyryl coenzyme A lithium salt; 103404-95-1. Cat No: COEC-055. | |
| Isovaleryl coenzyme A lithium salt hydrate | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Lauroyl coenzyme A lithium salt | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Lauroyl coenzyme A lithium salt | Lauroyl CoA is a substrate for FAM34A proteins and a product of firefly luciferase. Applications: A substrate for fam34a proteins. Group: Coenzymes. Synonyms: Dodecanoyl-Coenzyme A lithium salt. CAS No. 190063-12-8. Purity: ≥90%. Mole weight: 955.77. Appearance: Powder. Form: Solid. Dodecanoyl-Coenzyme A lithium salt; Lauroyl coenzyme A lithium salt; 190063-12-8. Cat No: COEC-056. | |
| Linoleoyl coenzyme A lithium salt | Linoleoyl coenzyme A lithium salt. CAS No: 103476-22-8 | Sarchem Laboratories New Jersey NJ |
| Malonyl-13C3 coenzyme A lithium salt | 99 atom % 13C, 95% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Malonyl coenzyme A lithium salt | Malonyl coenzyme A lithium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 108347-84-8. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C24H38N7O19P3S·xLi. US Biological Life Sciences. | Worldwide |
| Malonyl coenzyme A lithium salt | Malonyl coenzyme A lithium salt is a coenzyme A derivative of malonic acid. Malonyl CoA is involved in chain elongation during fatty acid and polyketide synthesis. Malonyl CoA is also used in transporting alpha-ketoglutarate across the mitochondrial membrane into the mitochondrial matrix. Applications: A coenzyme a derivative involved in fatty acid regulation and biosynthesis. Group: Coenzymes. CAS No. 108347-84-8. Purity: ≥90%. Mole weight: 853.58. Appearance: Powder. Form: Solid. Malonyl coenzyme A lithium salt; 108347-84-8. Cat No: COEC-009. | |
| Malonyl coenzyme A lithium salt | Malonyl coenzyme A lithium salt is a vital component in the biomedical industry used for studying metabolic processes and enzymatic reactions. It serves as a precursor in fatty acid biosynthesand plays a crucial role in cellular energy metabolism. Additionally, it aids in the research of various diseases related to malonyl-CoA metabolism dysfunctions. Synonyms: MALONYL COENZYME A LITHIUM SALT; malonyl coenzyme A lithium; coenzyme A malonyl derivative, lithium salt. Grades: ≥ 90% (HPLC). CAS No. 108347-84-8. Molecular formula: C24H38LiN7O19P3S. Mole weight: 860.6. | |
| ?-Methylcrotonyl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Myristoyl coenzyme A lithium salt | ?80.0%. Group: Fluorescence/luminescence spectroscopy. | |
| Myristoyl coenzyme A lithium salt | Myristoyl coenzyme A lithium salt. Group: Biochemicals. Alternative Names: n-Tetradecanoyl coenzyme A lithium salt. Grades: Highly Purified. CAS No. 187100-75-0. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C35H62N7O17P3S·xLi. US Biological Life Sciences. | Worldwide |
| Myristoyl coenzyme A lithium salt | Myristoyl coenzyme A lithium salt is a pivotal biomolecule occupying the role of a substrate. It manifests its indispensability in studying afflictions associated with lipid metabolism, notably encompassing cardiovascular ailments, obesity and cancer. Synonyms: n-Tetradecanoyl coenzyme A lithium salt. Molecular formula: C35H62N7O17P3S·xLi. Mole weight: 977.89 (free acid). | |
| n-Heptadecanoyl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| n-Heptadecanoyl coenzyme A lithium salt | n-Heptadecanoyl coenzyme A lithium salt. Applications: An acyl group carrier. Group: Coenzymes. CAS No. 3546-17-6. Mole weight: 1019.97. n-Heptadecanoyl coenzyme A lithium salt; 3546-17-6. Cat No: COEC-054. | |
| n-Propionyl coenzyme A lithium salt | ?85%. Group: Fluorescence/luminescence spectroscopy. | |
| n-Propionyl coenzyme A lithium salt | Propionyl coenzyme A (CoA) is the coenzyme A derivative of propionic acid. Propionyl CoA is formed during the β-oxidation of odd-chain fatty acids. Propionyl CoA is also formed during the metabolism of isoleucine and valine. Applications: The coenzyme a derivative of propionic acid. Group: Coenzymes. CAS No. 108321-21-7. Purity: ≥85%. Mole weight: 829.53. Appearance: Powder. Form: Solid. n-Propionyl coenzyme A lithium salt; 108321-21-7. Cat No: COEC-037. | |
| Octanoyl coenzyme A lithium salt | Octanoyl coenzyme A lithium salt acts as a acyl group carrier. This is a medium-chain fatty acid convalently linked to coenzyme A. Applications: A donor molecule for the octanylation of ghrelin and other peptides. Group: Coenzymes. Synonyms: Capryloyl coenzyme A lithium salt. CAS No. 324518-20-9. Purity: ≥95%. Mole weight: 893.73. Appearance: Powder. Form: Solid. Capryloyl coenzyme A lithium salt; Octanoyl coenzyme A lithium salt; 324518-20-9. Cat No: COEC-028. | |
| Octanoyl coenzyme a lithium salt hydrate | Octanoyl coenzyme a lithium salt hydrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: octanoylcoenzymealithiumsalthydrate, 324518-20-9. Product Category: Heterocyclic Organic Compound. CAS No. 324518-20-9. Molecular formula: C29H49N7O17P3S.Li.H2O. Mole weight: 917.682. Purity: 0.96. IUPACName: lithium;[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[hydroxy-[hydroxy-[3-hydroxy-2,2-dimethyl-4-[[3-(2-octanoylsulfanylethylamino)-3-oxopropyl]amino]-4-oxobutoxy]phosphoryl]oxyphosphoryl]oxymethyl]oxolan-3-yl] hydrogen phosphate;hydrate. Canonical SMILES: [Li+].CCCCCCCC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C2N=CN=C3N)O)OP(=O)(O)[O-])O.O. Product ID: ACM324518209. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Octanoyl coenzyme A lithium salt hydrate | ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Oleoyl-13C18 coenzyme A lithium salt | 99 atom % 13C, 95% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Oleoyl coenzyme A lithium salt | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Oleoyl coenzyme A lithium salt | Coenzyme A functions as an acyl group carrier, acetyl-CoA. Oleoyl coenzyme A (Oleoyl-CoA) may be used to study the specificity and kinetics of enzymes such as acyl-coenzyme A:cholesterol acyltransferase 1 (ACAT1) involved in long chain fatty acid cholesterol esterification. Applications: May be used to study the specificity and kinetics of enzymes such as acyl-coenzyme a:cholesterol acyltransferase 1 (acat1). Group: Coenzymes. Synonyms: cis-9-Octadecenoyl coenzyme A. CAS No. 188824-37-5. Purity: ≥90%. Mole weight: 1031.98. Appearance: Powder. Form: Solid. cis-9-Octadecenoyl coenzyme A; Oleoyl coenzyme A lithium salt; 188824-37-5. Cat No: COEC-058. | |
| Oleoyl coenzyme A lithium salt | Oleoyl coenzyme A lithium salt is a biomedical product aiding in exploration of lipid metabolism and cellular mechanisms. Acting as a linchpin in the intricate orchestration of fatty acid synthesis and degradation, this compound assumes a pivotal role in energy generation. Synonyms: cis-9-Octadecenoyl coenzyme A; tetralithium [(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[[[[(3R)-3-hydroxy-2,2-dimethyl-4-[[3-[2-[(Z)-octadec-9-enoyl]sulfanylethylamino]-3-oxopropyl]amino]-4-oxobutoxy]-oxidophosphoryl]oxy-oxidophosphoryl]oxymethyl]oxolan-3-yl] phosphate. Grades: ≥ 90%. CAS No. 188824-37-5. Molecular formula: C39H64Li4N7O17P3S. Mole weight: 1055.71. | |
| Palmitoleoyl coenzyme A lithium salt | ~90%. Group: Fluorescence/luminescence spectroscopy. | |
| Palmitoleoyl coenzyme A lithium salt | Palmitoleoyl coenzyme A lithium salt may be used in comparative long chain fatty acyl-CoA studies such as the effects of long-chain acyl-coenzyme A esters on cardiac K(ATP) channels and lipotoxic footprinting. Group: Coenzymes. Synonyms: cis-9-Hexadecenoyl Coenzyme A. CAS No. 18198-76-0. Purity: ≥90%. Mole weight: 1003.93. Form: Solid. cis-9-Hexadecenoyl Coenzyme A; Palmitoleoyl coenzyme A lithium salt; 18198-76-0. Cat No: COEC-057. | |
| Palmitoyl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Phenylacetyl coenzyme A lithium salt | Phenylacetyl coenzyme A lithium salt is used to study the phenylacetyl-CoA monooxygenase complex. Applications: Used to study the phenylacetyl-coa monooxygenase complex. Group: Coenzymes. CAS No. 108321-26-2. Purity: ≥95%. Mole weight: 885.67. Appearance: Powder. Form: Solid. Phenylacetyl coenzyme A lithium salt; 108321-26-2. Cat No: COEC-040. | |
| Propionyl coenzyme A lithium salt | Propionyl coenzyme A lithium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 108321-21-7. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C24H39N7O17P3SLi. US Biological Life Sciences. | Worldwide |
| Propionyl coenzyme A lithium salt | Propionyl coenzyme A lithium salt is a crucial compound used in biomedical field for its involvement in numerous biochemical processes. This product plays a vital role in energy metabolism as a cofactor, facilitating the conversion of propionic acid into succinyl coenzyme A. It is particularly valuable in studying diseases related to propionyl-CoA carboxylase deficiency. Synonyms: N-Propionyl coenzyme a lithium salt; lithium [ (2R, 3S, 4R, 5R) -5- (6-aminopurin-9-yl) -4-hydroxy-2- [ [hydroxy- [hydroxy- [3-hydroxy-2, 2-dimethyl-4-oxo-4- [ [3-oxo-3- (2-propanoylsulfanylethylamino) propyl] amino] butoxy] phosphoryl] oxyphosphoryl] oxymethyl] oxolan-3-yl] hydrogen phosphate. Grades: ≥ 90%. CAS No. 108321-21-7. Molecular formula: C24H39LiN7O17P3S. Mole weight: 829.53. | |
| Stearoyl-13C18 coenzyme A lithium salt | 99 atom % 13C, 95% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Stearoyl coenzyme A lithium salt | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Linoleoyl coenzyme A | Linoleoyl coenzyme A acts as a vital molecular precursor in the polyunsaturated fatty acid biosynthesis process. These fatty acids are necessary in various biological frameworks. It's a driving force in the biosynthesis of crucial mediating factors like prostaglandins, leukotrienes, and thromboxanes which have a central role in managing inflammation and pain. Moreover, linoleoyl coenzyme A is a pivotal agent in the metabolism of drugs and toxins, making it a fundamental area of interest when researching toxicology, and drug discovery. Synonyms: cis,cis-9,12-Octadecadienoyl coenzyme A; (9Z,12Z)-Octadecadienoyl-CoA; Linoleoyl coenzyme A lithium salt. Grades: ≥ 92% (HPLC). CAS No. 6709-57-5. Molecular formula: C39H66N7O17P3S. Mole weight: 1029.97. | |
| NAD+, Lithium salt | NAD+, Lithium salt is the salt form of NAD+, which is a coenzyme composed of ribosylnicotinamide 5'-diphosphate coupled to adenosine 5'-phosphate by pyrophosphate linkage. It plays a role in the activity of several enzymes, such as poly(ADP)-ribose polymerases and cADP-ribose synthases. NAD+ is commonly used as an oxidizing agent. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: β-Nicotinamide adenine Dinucleotide, Li; Beta-NAD lithium salt; Nicotinamide adenine dinucleotide lithium salt. CAS No. 64417-72-7. Molecular formula: C21H26LiN7O14P2. Mole weight: 669.362. | |
| NAD+, Lithium Salt | NAD+, Lithium Salt is a major electron acceptor molecule active in biological oxidations. Applications: A major electron acceptor compound active in biological oxidations. Group: Coenzymes. Synonyms: β-Nicotinamide-adenine Dinucleotide, Li. CAS No. 64417-72-7. Purity: ≥90%. Mole weight: 669.4. Form: Solid. β-Nicotinamide-adenine Dinucleotide, Li; NAD+, Lithium Salt; 64417-72-7. Cat No: COEC-025. | |
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