Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| Coenzyme A | Coenzyme A. CAS No: 85-61-0 |  Sarchem Laboratories New Jersey NJ |
| Coenzyme A | Coenzyme A (CoASH) is a ubiquitous and essential cofactor, which is an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Coenzyme A plays a central role in the oxidation of pyruvate in the citric acid cycle and the metabolism of carboxylic acids, including short- and long-chain fatty acids [1]. Uses: Scientific research. Group: Natural products. CAS No. 85-61-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-128851. |  |
| Coenzyme A | Coenzyme A is an essential metabolic cofactor synthesized from cysteine, pantothenate, and ATP. Coenzyme A plays important roles in many metabolic pathways, including the tricarboxylic acid cycle, and the synthesis and oxidation of fatty acids. About 4% of cellular enzymes utilize CoA as a substrate. Synonyms: CoASH; Coenzyme A (free acid); Depot-Zeel; Coenzyme ASH; 3'-phosphoadenosine 5'-{3-[ (3R) -3-hydroxy-2, 2-dimethyl-4-oxo-4- ({3-oxo-3-[ (2-sulfanylethyl) amino]propyl}amino) butyl] dihydrogen diphosphate}. Grades: >85%. CAS No. 85-61-0. Molecular formula: C21H36N7O16P3S. Mole weight: 767.53. |  |
| Coenzyme A free acid | 25mg Pack Size. Group: Analytical Reagents, Biochemicals, Flavours and Fragrance Materials. Formula: C21H36N7O16P3S. CAS No. 85-61-0. Prepack ID 66596238-25mg. Molecular Weight 767.53. See USA prepack pricing. |  |
| Coenzyme A, free acid | Coenzyme A (CoA, CoASH, or HSCoA) is a coenzyme, notable for its role in the synthesis and oxidation of fatty acids, and the oxidation of pyruvate in the citric acid cycle. All genomes sequenced to date encode enzymes that use coenzyme A as a substrate, and around 4% of cellular enzymes use it (or a thioester, such as acetyl-CoA) as a substrate. In humans, CoA biosynthesis requires cysteine, pantothenate, and adenosine triphosphate (ATP). Group: Coenzymes. Synonyms: Coenzyme A; CoA; Coenzyme A, free acid; 85-61-0; CoASH; HSCoA. CAS No. 85-61-0. Purity: > 75% when determined by enzymatic analysis with phosphotransacetylase at pH 7.5. CoA. Mole weight: 767.53 (as anhydrous free acid) 803.56 (CoA.2H2O). Storage: Keep tightly stoppered in the dark below 5°C. For Prolonged storage, keep below-20°C. Coenzyme A; CoA; Coenzyme A, free acid; 85-61-0; CoASH; HSCoA. Cat No: NATE-0145. |  |
| Coenzyme A - Free Acid | Supplement. CAS No. 85-61-0. |  US, Austria, Lithuania |
| Coenzyme A Lithium Salt | Supplement. CAS No. 18439-24-2. | US, Austria, Lithuania |
| Coenzyme A S-(2-Ethyl-3-oxobutanoate) | Coenzyme A S-(2-Ethyl-3-oxobutanoate). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H44N7O18P3S, Molecular Weight: 879.6. US Biological Life Sciences. |  Worldwide |
| Coenzyme A S-(2-Ethyl-3-oxobutanoate) | Coenzyme A S-(2-Ethyl-3-oxobutanoate) is an derivative of Coenzyme A, a cofactor in enzymatic acetyl transfer reactions. Molecular formula: C27H44N7O18P3S. Mole weight: 879.6. | |
| Coenzyme A sodium | Coenzyme A (CoASH) sodium is a ubiquitous and essential cofactor, which is an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Coenzyme A plays a central role in the oxidation of pyruvate in the citric acid cycle and the metabolism of carboxylic acids, including short- and long-chain fatty acids [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 55672-92-9. Pack Sizes: 5 mg; 10 mg. Product ID: HY-128851B. | |
| Coenzyme A sodium salt | This compound is an essential cofactor in enzymatic acetyl transfer reactions. Applications: An essential cofactor in enzymatic acetyl transfer reactions. Group: Coenzymes. Synonyms: CoA Na2. CAS No. 55672-92-9. Purity: ≥90%. Mole weight: 767.53. Appearance: Powder. Form: Solid. CoA Na2; Coenzyme A sodium salt; 55672-92-9. Cat No: COEC-003. | |
| Coenzyme A Sodium Salt | Supplement. CAS No. 55672-92-9. Categories: c21h36n7o16p3s.xna, c21-h36-n7-o16-p3-s.x-na, coenzyme a sodium salt hydrate, 55672-92-9. | US, Austria, Lithuania |
| Coenzyme A S-Pyrazinecarboxylate Trisodium Salt | Coenzyme A S-Pyrazinecarboxylate is a derivative of Coenzyme A; a cofactor in enzymatic acetyl transfer reactions. It is the source of the phosphopantetheine group that is added as a prosthetic group to proteins such as acyl carrier protein and formyltetrahydrofolate dehydrogenase. Synonyms: S- (2- (3- ( (2R) -4- ( ( ( ( ( ( (2R, 3S, 4R, 5R) -5- (6-Amino-9H-purin-9-yl) -4-hydroxy-3- (phosphonooxy) tetrahydrofuran-2-yl) methoxy) (hydroxy) phosphoryl) oxy) (hydroxy) phosphoryl) oxy) -2-hydroxy-3, 3-dimethylbutanamido) propanamido) ethyl) Pyrazine-2-carbothioate Trisodium Salt. Molecular formula: C26H35N9Na3O17P3S. Mole weight: 939.56. | |
| Coenzyme A trilithium | Coenzyme A (CoASH) is a ubiquitous and essential cofactor, which is an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Coenzyme A plays a central role in the oxidation of pyruvate in the citric acid cycle and the metabolism of carboxylic acids, including short- and long-chain fatty acids [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 18439-24-2. Pack Sizes: 10 mg. Product ID: HY-128851A. | |
| Coenzyme A Trilithium Salt | A cofactor in enzymatic acetyl transfer reactions. It is the source of the phosphopantetheine group that is added as a prosthetic group to proteins such as acyl carrier protein and formyltetrahydrofolate dehydrogenase. Synonyms: CoA Trilithium Salt; Trilithium Coenzyme A. Grades: 95%. CAS No. 18439-24-2. Molecular formula: C21H33Li3N7O16P3S. Mole weight: 785.33. | |
| 04:1 Coenzyme A Sodium salt | 04:1 Coenzyme A Sodium salt is a fundamental biochemical compound prevalent in the biomedical sector, demonstrating its indispensability as a coenzyme involved in diverse metabolic pathways. Its remarkable functionality aids in the seamless transfer of acyl groups. Moreover, owing to its profound impact on lipid metabolism, this product emerges as a potential solution in the treatment of metabolic afflictions, including obesity, diabetes, and cardiovascular anomalies. Synonyms: (E)-but-2-enoyl Coenzyme A (sodium salt); sodium (2R, 3S, 4R, 5R) -5- (6-amino-9H-purin-9-yl) -2- ( ( ( ( ( ( (R) -4- ( (3- ( (2- ( ( (E) -but-2-enoyl) thio) ethyl) amino) -3-oxopropyl) amino) -3-hydroxy-2, 2-dimethyl-4-oxobutoxy) oxidophosphoryl) oxy) oxidophosphoryl) oxy) methyl) -4-hydroxytetrahydrofuran-3-yl hydrogen phosphate; 9H-Purin-6-amine, 9- [ (2ξ ) -5-O- [hydroxy [ [hydroxy [ (3R) -3-hydroxy-2, 2-dimethyl-4-oxo-4- [ [3-oxo-3- [ [2- [ [ (2E) -1-oxo-2-buten-1-yl] thio] ethyl] amino] propyl] amino] butoxy] phosphinyl] oxy] phosphinyl] -3-O-phosphono-β -D-threo-pentofuranosyl] -, sodium salt (1:3). Grades: >99%. CAS No. 2260670-60-6. Molecular formula: C25H37N7Na3O17P3S. Mole weight: 901.55. | |
| 12:0 Biotinyl Coenzyme A | 12:0 Biotinyl Coenzyme A. Group: Others. Purity: >99%. Mole weight: 1241.45. Stability: 6 Months. Storage: -20°C. Avanti Polar Lipids; lipid products; natural lipids; natural; synthetic lipid; synthetic; modified lipids; headgroup modified lipids; fatty acid modified lipids; singnal transduction; cell pathways; 12:0 Biotinyl Coenzyme A; 12-N-biotinyl(aminododecanoyl) Coenzyme A (ammonium salt). Cat No: NSMZ-111. | |
| 16:0 Azido Coenzyme A Ammonium salt | 16:0 Azido Coenzyme A Ammonium salt is a biochemical reagent mostly used in research related to lipid metabolism and protein modification studies. This product can also help to investigate possible new treatment approaches for metabolic disorders or diseases. Synonyms: 16-azidohexadecanoyl Coenzyme A (ammonium salt). Grades: >99%. CAS No. 2260670-37-7. Molecular formula: C37H74N13O17P3S. Mole weight: 1098.05. | |
| 18:1 Ether Coenzyme A Ammonium salt | 18:1 Ether Coenzyme A Ammonium salt, a crucial ingredient in synthesizing glycosphingolipids and phospholipids, holds an instrumental position in the oxidative disposal of fatty acids while also being a vital agent for drug and toxin metabolism. It is a medically potent recourse for lipid abnormalities and certain inherited metabolic disorders, offering a path of primacy for therapeutic intervention. Synonyms: (9Z-octadecenyl) Coenzyme A (ammonium salt); triazanium (2R, 3S, 4R, 5R) -5- (6-amino-9H-purin-9-yl) -4-hydroxy-2- ( ( ( ( ( ( (R) -3-hydroxy-2, 2-dimethyl-4- ( (3- ( (2- ( ( (Z) -octadec-9-en-1-yl) thio) ethyl) amino) -3-oxopropyl) amino) -4-oxobutoxy) oxidophosphoryl) oxy) oxidophosphoryl) oxy) methyl) tetrahydrofuran-3-yl hydrogen phosphate; 9H-Purin-6-amine, 9-[(2ξ)-5-O-[hydroxy[[hydroxy[(3R)-3-hydroxy-2,2-dimethyl-4-[[3-[[2-[(9Z)-9-octadecen-1-ylthio]ethyl]amino]-3-oxopropyl]amino]-4-oxobutoxy]phosphinyl]oxy]phosphinyl]-3-O-phosphono-β-D-threo-pentofuranosyl]-, triammonium salt. Grades: >99%. CAS No. 2260670-62-8. Molecular formula: C39H79N10O16P3S. Mole weight: 1068.46. | |
| 28:0 Coenzyme A Ammonium salt | 28:0 Coenzyme A Ammonium salt, a fundamental element in the regulation of fatty acid metabolism, serves an integral role in the intricate beta-oxidation process. Traditionally deployed as a metabolic biomarker for detecting metabolic aberrations (namely obesity, diabetes, and cardiovascular maladies), research also suggests possibilities for its incorporation in ameliorative measures against metabolic disorders as well as cancerous growths. Synonyms: Octacosanoyl Coenzyme A (ammonium salt); 9H-Purin-6-amine, 9- [ (2ξ ) -5-O- [hydroxy [ [hydroxy [ (3R) -3-hydroxy-2, 2-dimethyl-4-oxo-4- [ [3-oxo-3- [ [2- [ (1-oxooctacosyl) thio] ethyl] amino] propyl] amino] butoxy] phosphinyl] oxy] phosphinyl] -3-O-phosphono-β -D-threo-pentofuranosyl] -, ammonium salt. Grades: >99%. CAS No. 2260795-80-8. Molecular formula: C49H99N10O17P3S. Mole weight: 1225.37. | |
| 2-Butenoyl coenzyme A lithium salt | 2-Butenoyl coenzyme A lithium salt. CAS No: 102680-35-3 | Sarchem Laboratories New Jersey NJ |
| 2-Ethyl-3-Hydroxybutyryl Coenzyme A | 2-Ethyl-3-Hydroxybutyryl Coenzyme A. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H46N7O18P3S, Molecular Weight: 881.68. US Biological Life Sciences. | Worldwide |
| 2-Ethyl-3-Hydroxybutyryl Coenzyme A | 2-Ethyl-3-Hydroxybutyryl Coenzyme A is a derivative of Coenzyme A, a cofactor in enzymatic acetyl transfer reactions. 2-Ethyl-3-Hydroxybutyryl Coenzyme A has been used to study Rathke's pouch homeobox (RPX), a novel antierior-restricted homeobox gene progressively activated in prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo. Molecular formula: C27H46N7O18P3S. Mole weight: 881.68. | |
| 2-Ethyl-3-oxobutyryl Coenzyme A | 2-Ethyl-3-oxobutyryl Coenzyme A. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H44N7O18P3S, Molecular Weight: 879.66. US Biological Life Sciences. | Worldwide |
| 2-Ethyl-3-oxobutyryl Coenzyme A | 2-Ethyl-3-oxobutyryl Coenzyme A is a derivative of Coenzyme A, a cofactor in enzymatic acetyl transfer reactions. 2-Ethyl Crotonyl Coenzyme A has been used to study Rathke's pouch homeobox (RPX), a novel antierior-restricted homeobox gene progressively activated in prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo. Molecular formula: C27H44N7O18P3S. Mole weight: 879.66. | |
| 2-Ethylbutyryl Coenzyme A | 2-Ethylbutyryl Coenzyme A. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H46N7O17P3S, Molecular Weight: 865.68. US Biological Life Sciences. | Worldwide |
| 2-Ethylbutyryl Coenzyme A | 2-Ethylbutyryl Coenzyme A is a Coenzyme A derivative, a cofactor in enzymatic acetyl transfer reactions. 2-Ethylbutyryl Coenzyme A has been used to study Rathke's pouch homeobox (RPX), a novel antierior-restricted homeobox gene progressively activated in prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo. Molecular formula: C27H46N7O17P3S. Mole weight: 865.68. | |
| 2-Ethyl Crotonyl Coenzyme A | 2-Ethyl Crotonyl Coenzyme A. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C27H44N7O17P3S, Molecular Weight: 863.66. US Biological Life Sciences. | Worldwide |
| 2-Ethyl Crotonyl Coenzyme A | 2-Ethyl Crotonyl Coenzyme A is a Coenzyme A derivative, a cofactor in enzymatic acetyl transfer reactions. 2-Ethyl Crotonyl Coenzyme A has been used to study Rathke's pouch homeobox (RPX), a novel antierior-restricted homeobox gene progressively activated in prechordal plate, anterior neural plate and Rathke's pouch of the mouse embryo. Molecular formula: C27H44N7O17P3S. Mole weight: 863.66. | |
| 30:0 Coenzyme A Ammonium salt | 30:0 Coenzyme A Ammonium salt is a complex biochemical compound employed for the purpose of exploring and investigating the intricate subject of fatty acid metabolism. As a catalyzing cofactor, it actively participates in the enzymatic reactions integral to the beta-oxidation of very long chain fatty acids (VLCFAs), playing a central role in the treatment of X-linked adrenoleukodystrophy (X-ALD) and Zellweger syndrome, among other related disorders. Synonyms: Triacontanoyl Coenzyme A (ammonium salt). Grades: >99%. CAS No. 2260795-81-9. Molecular formula: C51H103N10O17P3S. Mole weight: 1253.42. | |
| 6',10',14'-Hexahydro 4-Dehydro Coenzyme Q4 | 6',10',14'-Hexahydro 4-Dehydro Coenzyme Q4 can be obtained from (E,E)-Farnesol (F102430) which is a natural organic compound which is present in many essential oils. Analytical Standard, Impurity of Drug. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C29H46O4, Molecular Weight: 458.67. US Biological Life Sciences. | Worldwide |
| Acetoacetyl coenzyme A | Acetoacetyl coenzyme A is a coenzyme. Applications: A coenzyme. Group: Coenzymes. Synonyms: S-Acetoacetylcoenzyme A. CAS No. 1420-36-6. Mole weight: 851.61. S-Acetoacetylcoenzyme A; Acetoacetyl coenzyme A; 1420-36-6. Cat No: COEC-036. | |
| 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. | |
| Acetoacetyl coenzyme A trisodium salt tetrahydrate | Acetoacetyl Coenzyme A Trisodium Salt Tetrahydrate is used in the biomedical industry for its role as a metabolic intermediate. Acetoacetyl Coenzyme A Trisodium Salt Tetrahydrate is involved in the bioresearch and development of various ketone bodies, which are utilized as an energy source during conditions such as fasting or exercise. Additionally, it plays a crucial role in drug development, specifically for compounds targeting diseases related to abnormal fat metabolism. Synonyms: Acetoacetyl-CoANa3 tetrahydrate. Grades: 96%. CAS No. 102029-52-7. Molecular formula: C25H37N7Na3O18P3S·4H2O. Mole weight: 989.62. | |
| Acetyl coenzyme A | Acetyl coenzyme A is the precursor to HMG CoA, an essential component in the synthesis of cholesterol and ketone. Synonyms: Acetyl-CoA; S-Acetyl coenzyme A; AcCoA; Coenzyme A, S-acetate; S-acetyl-CoA. CAS No. 72-89-9. Molecular formula: C23H38N7O17P3S. Mole weight: 809.57. | |
| Acetyl-Coenzyme A acetyltransferase 2 from Human, Recombinant | ACAT2 enzyme participates in lipid metabolism. ACAT2 takes part in lipoprotein assembly, catalyzing cholesterol esterification in mammalian cells. ACAT2 is an integral membrane protein that localizes to the endoplasmic reticulum of human intestinal cells. ACAT2 deficiency contributes to severe mental retardation and hypotonus. Acat2 recombinant human produced in e. coli is a single, non-glycosylated polypeptide chain containing 433 amino acids (1-397 a.a.) and having a molecular mass of 45.4 kda. the acat2 is fused to 36 amino acid his-tag at n-terminus and purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: Acetyl-CoA acetyltransferase cytosolic; Cytosolic acetoacetyl-CoA thiolase; ACAT2; Acetyl CoA transferase-like protein; ACAT-2. Purity: Greater than 95.0% as determined by SDS-PAGE. ACAT-2. Mole weight: 45.4 kDa. Stability: ACAT2 Human although stable at 4°C for 1 week, should be stored desiccated below -18°C. Please prevent freeze thaw cycles. Appearance: Sterile Filtered clear solution. Source: E. coli. Species: Human. Acetyl-CoA acetyltransferase cytosolic; Cytosolic acetoacetyl-CoA thiolase; ACAT2; Acetyl CoA transferase-like protein; ACAT-2. Cat No: NATE-0798. | |
| Acetyl coenzyme A lithium | Acetyl-coenzyme A (Acetyl-CoA) lithium is a membrane-impermeant central metabolic intermediate, participates in the TCA cycle and oxidative phosphorylation metabolism. Acetyl-coenzyme A lithium, regulates various cellular mechanisms by providing (sole donor) acetyl groups to target amino acid residues for post-translational acetylation reactions of proteins. Acetyl Coenzyme A lithium is also a key precursor of lipid synthesis [1] [2] [3] [4]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Acetyl-CoA lithium. CAS No. 32140-51-5. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-113596A. | |
| 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. | |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt, a pivotal molecule in the biomedical industry, is widely utilized in fatty acid and cholesterol biosynthesis, as well as the citric acid cycle. Its role in drug and toxin metabolism and breakdown in the body is also noteworthy. Besides, it contributes to treating metabolic disorders such as diabetes, obesity, and cancer. Its multifaceted functions make it a molecule of great scientific significance. Synonyms: Acetyl CoA. Grades: 90%. CAS No. 102029-73-2. Molecular formula: C23H38N7O17P3S·xNa. Mole weight: 809.57 (free acid). | |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt. Group: Biochemicals. Alternative Names: Acetyl CoA. Grades: Highly Purified. CAS No. 102029-73-2. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C23H38N7O17P3S·xNa. US Biological Life Sciences. | Worldwide |
| Acetyl coenzyme A sodium salt | Acetyl coenzyme A sodium salt is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. 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. It is a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Also a positive regulator of pyruvate carboxylase and a precursor of the neurotransmitter acetylcholine. Applications: An essential cofactor and carrier of acyl groups. Group: Coenzymes. Synonyms: Acethyl coenzyme alpha sodium salt. CAS No. 102029-73-2. Purity: ≥92%. Mole weight: 893.53. Appearance: Powder. Form: Solid. Acethyl coenzyme alpha sodium salt; Acetyl coenzyme A sodium salt; 102029-73-2. Cat No: COEC-047. | |
| Acetyl coenzyme A trilithium salt | Acetyl coenzyme A trilithium salt, an indispensable biochemical constituent extensively utilized in the biomedicine realm, assumes an pivotal role as a vital coenzyme within diverse metabolic pathways, engendering the synthesis and decomposition of molecules within the human anatomical framework. Synonyms: Acetyl-S-CoA Li3. Grades: 95%. CAS No. 75520-41-1. Molecular formula: C23H35Li3N7O17P3S. Mole weight: 827.37. | |
| Acetyl coenzyme A trilithium salt | Acetyl coenzyme A trilithium salt. Group: Biochemicals. Alternative Names: Acetyl-S-CoA Li3. Grades: Highly Purified. CAS No. 75520-41-1. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C23H35Li3N7O17P3S. US Biological Life Sciences. | Worldwide |
| Acetyl coenzyme A trilithium salt trihydrate | Acetyl coenzyme A trilithium salt trihydrate is a crucial compound utilized in various biochemical processes, particularly in the tricarboxylic acid cycle and fatty acid research. This compound is beneficial in studying disorders related to metabolism, such as fatty acid oxidation disorders and certain neurodegenerative diseases. Synonyms: Acetyl CoALi3. CAS No. 496948-93-7. Molecular formula: C23H35N7O17P3S.3Li. Mole weight: 827.37. | |
| Acetyl Coenzyme A Trilithium Salt Trihydrate | Acetyl Coenzyme A Trilithium Salt Trihydrate is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. It is also the precursor for lipid biosynthesis and the neurotransmitter acetylcholine. Applications: An essential cofactor. Group: Coenzymes. CAS No. 75520-41-1. Mole weight: 881.42. Appearance: Powder. Form: Solid. Acetyl Coenzyme A Trilithium Salt Trihydrate; 75520-41-1. Cat No: COEC-100. | |
| Acyl-Coenzyme A Dehydrogenase 8 from Human, Recombinant | Acyl CoA dehydrogenase is the enzymeused to catalyzethe first step of β-oxidationin Fatty acid metabolism. Acyl-coenzyme A (CoA) dehydrogenases (ACADs) are a family of mitochondrial enzymes that catalyze the first dehydrogenation step in the bets-oxidation of fatty acyl-CoA derivatives. Several human ACADs exist and all ACADs catalyze the same initial dehydrogenation of the substrate at the beta-carbon atom and require electron transfer flavoprotein as an alectron acceptor. The predicted 415-amino acid ACAD8 protein contains many of the residues conserved in most other ACADs, including an active site glutamic acid residue and residues important for tetramer f...mber 8 mitochondrial; ACAD-8; Isobutyryl-CoA dehydrogenase; Activator-recruited cofactor 42 kDa component; ARC42; FLJ22590. Purity: Greater than 95.0% as determined by SDS-PAGE. ACAD-8. Mole weight: 47.7 kDa. Stability: ACAD8 although stable at 4°C for 1 week, should be stored desiccated below -18°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please prevent freeze-thaw cycles. Appearance: Sterile Filtered clear solution. Source: E. coli. Species: Human. Acyl-CoA dehydrogenase family member 8 mitochondrial; ACAD-8; Isobutyryl-CoA dehydrogenase; Activator-recruited cofactor 42 kDa component; ARC42; FLJ22590. Cat No: NATE-0801. | |
| Acyl coenzyme A synthetase | Acyl coenzyme A synthetase (ACS), namely acetyl coenzyme A synthetase, is often used in biochemical research. Acyl coenzyme A synthetase can catalyze the activation of fatty acids by coenzyme A through a two-step thioesterification reaction to produce acyl coenzyme A, and then participate in a variety of anabolic and catabolic lipid metabolism pathways, and participate in the TCA cycle in aerobic respiration [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ACS. CAS No. 9013-18-7. Pack Sizes: 100 U. Product ID: HY-P2832. | |
| ACYL-COENZYME A SYNTHETASE | ACYL-COENZYME A SYNTHETASE. Synonyms: EC 6.2.1.3;ACID: COA LIGASE (AMP-FORMING);ACYL-COENZYME A SYNTHETASE;Synthetase, acyl coenzyme A;ACYL-COENZYME A SYNTHETASE FROM PSEUDO-M ONAS SP., ~2.5U/MG;acyl-coenzyme a synthetase from pseudomonas sp.;Acyl-coenzyme A Synthetase [>=8 units/mg];Acyl-CoA Synthetase. CAS No. 9013-18-7. Pack Sizes: 1 kg. Product ID: CDF4-0057. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; ACYL-COENZYME A SYNTHETASE; CDF4-0057; 9013-18-7; 232-747-5; 9013-18-7. Purity: 0.99. Color: White. EC Number: 232-747-5. Physical State: Powder. Storage: -20°C. Product Description: Acyl-coenzyme A synthetase belongs to adenylate-forming enzymes superfamily. It has a conserved adenosine triphosphate/adenosine monophosphate (ATP/AMP) binding motif. |  |
| 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. | |
| Azo Coenzyme A Triammonium salt | Azo Coenzyme A Triammonium Salt, a fundamental biochemical reagent, holds momentous implications in exploring enzymatic reactions that involve coenzyme A and its various derivatives. This reagent remarkably aids in the synthesis of inhibitors for the acetyl-CoA carboxylase enzyme, which is crucial for fatty acid synthesis. The said reagent has also been scrutinized for its potential applications in treating metabolic disorders, hyperlipidemia and other related conditions, thereby signifying relatively consequential implications in the field of life sciences. Synonyms: (E)-4-(4-((4-butylphenyl)diazenyl)phenyl)butanoyl Coenzyme A (ammonium salt); 9H-Purin-6-amine, 9- [ (2ξ ) -5-O- [ [ [ [ (3R) -4- [ [3- [ [2- [ [4- [4- [ (E) -2- (4-butylphenyl) diazenyl] phenyl] -1-oxobutyl] thio] ethyl] amino] -3-oxopropyl] amino] -3-hydroxy-2, 2-dimethyl-4-oxobutoxy] hydroxyphosphinyl] oxy] hydroxyphosphinyl] -3-O-phosphono-β -D-threo-pentofuranosyl] -, ammonium salt; Coenzyme A, S-[4-[ (1E) -2- (4-Butylphenyl) diazenyl]benzenebutanoate], ammonium salt. Grades: >99%. CAS No. 2260670-58-2. Molecular formula: C41H67N12O17P3S. Mole weight: 1125.03. | |
| 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 |
| β-NAD, Oxidized (Beta-NAD, Coenzyme I) | β-NAD, Oxidized (Beta-NAD, Coenzyme I). Group: Biochemicals. Alternative Names: Adenosine 5-(Trihydrogen Diphosphate), P?5-Ester with 3-(Aminocarbonyl)-1- β -D-ribofuranosyl pyridinium Hydroxide, Inner Salt; Pyridinium, 3-Carbamoyl-1- β-D-ribofuranosyl-, Hydroxide, 5?5-Ester with Adenosine 5-(Trihydrogen Pyrophosphate), Inner Salt (8CI); Adenine-nicotinamide Dinucleotide; CO-I; Codehydrase I; Codehydrogenase I; Coenzyme I; Cozymase I; DPN; Diphosphopyridine Nucleotide; Enzopride; NAD; NAD+; NSC 20272; Nadide; Nicotinamide-adenine Dinucleotide; Oxidized Diphosphopyridine Nucleotide; β-Diphosphopyridine Nucleotide; β-NAD; β-NAD+; β-Nicotinamide Adenine Dinucleotide; β-Nicotinamide Adenine Dinucleotide Hydrate. Grades: Highly Purified. CAS No. 53-84-9. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| Biotin (D-Biotin, Vitamin H, Coenzyme R, Bioepiderm) | Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanoic Acid; (+)-Biotin; Vitamin B7; Coenzyme R; D(+)-Biotin; Factor S; Lutavit H2; Meribin; NSC 63865; Rovimix H2. Grades: Molecular Biology Grade. CAS No. 58-85-5. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C??H??N?O?S, Molecular Weight: 244.31. US Biological Life Sciences. | Worldwide |
| Biotin (D-Biotin, Vitamin H, Coenzyme R, Bioepiderm), 97.5-100.5% USP | Biotin (D-Biotin, Vitamin H, Coenzyme R, Bioepiderm), 97.5-100.5% USP. Group: Biochemicals. Alternative Names: (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanoic Acid; (+)-Biotin; Vitamin B7; Coenzyme R; D(+)-Biotin; Factor S; Lutavit H2; Meribin; NSC 63865; Rovimix H2. Grades: USP. CAS No. 58-85-5. Pack Sizes: 1g, 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Biotinyl coenzyme A | Biotinyl coenzyme A. Group: Biochemicals. Alternative Names: 12-N-biotinyl (aminododecanoyl) Coenzyme A ammonium salt. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg, 10mg. US Biological Life Sciences. | Worldwide |
| Biotinyl coenzyme A | Biotinyl coenzyme A, known scientifically as 5'-deoxyadenos-5'-ylmethylthioadenylate is a pivotal and indispensable compound widely employed in the facilitation of crucial metabolic routes, mainly the carboxylation of intricate fatty acids and amino acids as well as the development of glucose. Synonyms: 12-N-biotinyl(aminododecanoyl) Coenzyme A ammonium salt. Molecular formula: C43H82N13O19P3S2. Mole weight: 1242.24. | |
| 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 hydrate | Butyryl-Coenzyme A lithium hydrate can synthesize Butyric acid (HY-B0350) or Butyrate [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Butyryl CoA lithium hydrate. CAS No. 1107039-35-9. Pack Sizes: 500 μg; 1 mg. Product ID: HY-141479B. | |
| coenzyme-B sulfoethylthiotransferase | This enzyme catalyses the final step in methanogenesis, the biological production of methane. This important anaerobic process is carried out only by methanogenic archaea. The enzyme can also function in reverse, for anaerobic oxidation of methane.The enzyme requires the hydroporphinoid nickel complex coenzyme F430. Highly specific for coenzyme B with a heptanoyl chain; ethyl CoM and difluoromethyl CoM are poor substrates. The sulfide sulfur can be replaced by selenium but not by oxygen. Group: Enzymes. Synonyms: methyl-CoM reductase; methyl coenzyme M reductase. Enzyme Commission Number: EC 2.8.4.1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3427; coenzyme-B sulfoethylthiotransferase; EC 2.8.4.1; methyl-CoM reductase; methyl coenzyme M reductase. Cat No: EXWM-3427. | |
| coenzyme F420-0:L-glutamate ligase | This protein catalyses the successive addition of two glutamate residues to cofactor F420 by two distinct and independent reactions. In the reaction described here the enzyme attaches a glutamate via its α-amine group to F420-0. In the second reaction (EC 6.3.2.34, coenzyme F420-1-γ-L-glutamate ligase) it catalyses the addition of a second L-glutamate residue to the γ-carboxyl of the first glutamate. Group: Enzymes. Synonyms: CofE-AF; MJ0768; CofE. Enzyme Commission Number: EC 6.3.2.31. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5748; coenzyme F420-0:L-glutamate ligase; EC 6.3.2.31; CofE-AF; MJ0768; CofE. Cat No: EXWM-5748. | |
| coenzyme F420-1:γ-L-glutamate ligase | This protein catalyses the successive addition of two glutamate residues to cofactor F420 by two distinct and independent reactions. In the first reaction (EC 6.3.2.31, coenzyme F420-0-L-glutamate ligase) the enzyme attaches a glutamate via its α-amine group to F420-0. In the second reaction, which is described here, the enzyme catalyses the addition of a second L-glutamate residue to the γ-carboxyl of the first glutamate. Group: Enzymes. Synonyms: F420:γ-glutamyl ligase; CofE-AF; MJ0768; CofE. Enzyme Commission Number: EC 6.3.2.34. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5751; coenzyme F420-1:γ-L-glutamate ligase; EC 6.3.2.34; F420:γ-glutamyl ligase; CofE-AF; MJ0768; CofE. Cat No: EXWM-5751. | |
| coenzyme F420H2 oxidase | The enzyme contains FMN and a binuclear iron center. The enzyme from the archaeon Methanothermobacter marburgensis is Si-face specific with respect to C-5 of coenzyme F420. Group: Enzymes. Synonyms: FprA. Enzyme Commission Number: EC 1.5.3.22. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1550; coenzyme F420H2 oxidase; EC 1.5.3.22; FprA. Cat No: EXWM-1550. | |
| coenzyme F420 hydrogenase | An iron-sulfur flavoprotein (FAD) containing nickel. The enzyme from some sources contains selenocysteine. The enzyme also reduces the riboflavin analogue of F420, flavins and methylviologen, but to a lesser extent. The hydrogen acceptor coenzyme F420 is a deazaflavin derivative. Group: Enzymes. Synonyms: 8-hydroxy-5-deazaflavin-reducing hydrogenase; F420-reducing hydrogenase; coenzyme F420-dependent hydrogenase. Enzyme Commission Number: EC 1.12.98.1. CAS No. 9027-5-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0524; coenzyme F420 hydrogenase; EC 1.12.98.1; 9027-05-8; 8-hydroxy-5-deazaflavin-reducing hydrogenase; F420-reducing hydrogenase; coenzyme F420-dependent hydrogenase. Cat No: EXWM-0524. | |
| coenzyme F420 oxidoreductase (ferredoxin) | The enzyme from the archaeon Methanosarcina mazei contains iron-sulfur centres and FAD. Group: Enzymes. Synonyms: Fd:F420 oxidoreductase; FpoF protein; ferredoxin:F420 oxidoreductase. Enzyme Commission Number: EC 1.5.7.2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1559; coenzyme F420 oxidoreductase (ferredoxin); EC 1.5.7.2; Fd:F420 oxidoreductase; FpoF protein; ferredoxin:F420 oxidoreductase. Cat No: EXWM-1559. | |
| coenzyme γ-F420-2:α-L-glutamate ligase | The enzyme caps the γ-glutamyl tail of the hydride carrier coenzyme F420. Group: Enzymes. Synonyms: MJ1001; CofF protein; γ-F420-2:α-L-glutamate ligase. Enzyme Commission Number: EC 6.3.2.32. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5749; coenzyme γ-F420-2:α-L-glutamate ligase; EC 6.3.2.32; MJ1001; CofF protein; γ-F420-2:α-L-glutamate ligase. Cat No: EXWM-5749. | |
| Coenzyme Q10 EP Impurity A | Coenzyme Q10 EP Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 2,3-dimethoxy-5-methylbenzene-1,4-diol. CAS No. 3066-90-8. Molecular Formula: C9H12O4. Mole Weight: 184.19. Catalog: APB3066908. |  |
Our database is helping our users find suppliers everyday.
