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| Product | Description | |
|---|---|---|
| Pantothenic Acid-13C3,15N Hemicalcium Salt | Labeled Pantothenic Acid. Group: Biochemicals. Alternative Names: N-[(2R)-2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl]-15N Hemicalcium; Pantothenic Acid-13C3,15N Hemicalcium; Vitamin B3-13C3,15N Hemicalcium; Vitamin B5. Grades: Highly Purified. CAS No. 356786-94-2. Pack Sizes: 1mg. US Biological Life Sciences. |  Worldwide |
| Pantothenic Acid (Technical Grade, Contains Lactone) | Pantothenic Acid is a member of the B complex vitamins; essential vitamin for the biosynthesis of coenzyme A in mammalian cells. Occurs ubiquitously in all animal and plant tissue. The richest common source is liver, but jelly of the queen bee contains 6 times as much as liver. Rice bran and molasses are other good sources. Group: Biochemicals. Grades: Purified. CAS No. 79-83-4. Pack Sizes: 1g, 10g. Molecular Formula: C9H17NO5. US Biological Life Sciences. | Worldwide |
| 4-O-(b-D-Glucopyranosyl)-D-pantothenic acid | 4-O-(b-D-Glucopyranosyl)-D-pantothenic acid is an esteemed compound, applied predominantly in the pharmaceutical sector of afflictions, encompassing diabetes, cardiovascular disorders and neuronal dysfunctions. Its remarkable advantages reside in its adeptness to selectively modulate intricate cellular cascades and pathways that underlie the aforementioned maladies. Synonyms: D-Pantothenic acid 4-O-b-glucoside. CAS No. 29493-59-2. Molecular formula: C15H27NO10. Mole weight: 381.38. |  |
| D-Pantothenic acid | D-Pantothenic acid (Pantothenate) is an essential trace nutrient that functions as the obligate precursor of coenzyme A (CoA). D-Pantothenic acid plays key roles in myriad biological processes, including many that regulate carbohydrate, lipid, protein, and nucleic acid metabolism [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Pantothenate; Vitamin B5. CAS No. 79-83-4. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0430. |  |
| D-(+)-Pantothenic acid calcium salt | D-(+)-Pantothenic acid calcium salt. Synonyms: D-Pantothenic acid hemicalcium salt, (R)-(+)-N-(2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl)-β-alanine hemicalcium salt, Calcium D-pantothenate, Vitamin B5. CAS No. 137-08-6. Pack Sizes: 1 kg. Product ID: CDC10-0382. Molecular formula: C18H32CaN2O10. Category: Cosmetic Surfactants. Product Keywords: Cosmetic Ingredients; Cosmetic Surfactants; D-(+)-Pantothenic acid calcium salt; CDC10-0382; 137-08-6; C18H32CaN2O10; D-Pantothenic acid hemicalcium salt, (R)-(+)-N-(2,4-Dihydroxy-3,3-dimethyl-1-oxobutyl)-β-alanine hemicalcium salt, Calcium D-pantothenate, Vitamin B5; 205-278-9; MFCD00002766; 137-08-6. Purity: 0.99. EC Number: 205-278-9. Physical State: White Crystalline Powder. Storage: 2-8°C. Boiling Point: 551.5°C at 760 mmHg. Melting Point: 190°C. Density: 1.266 g/cm3. |  |
| D-Pantothenic acid calcium salt | 100g Pack Size. Group: Biochemicals, Building Blocks, Organics. Formula: C18H32CaN2O10. CAS No. 137-08-6. Prepack ID 27765940-100g. Molecular Weight 476.54. See USA prepack pricing. |  |
| D-Pantothenic acid calcium salt | 500g Pack Size. Group: Biochemicals, Building Blocks, Organics. Formula: C18H32CaN2O10. CAS No. 137-08-6. Prepack ID 27765940-500g. Molecular Weight 476.54. See USA prepack pricing. | |
| D-Pantothenic Acid Calcium Salt | Pantothenic acid (vitamin B5) is a precursor in the biosynthesis of coenzyme A, which is an essential cofactor functioning as an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Two enantiomers of pantothenic acid exist, D- or L-form. D-Pantothenic acid (sodium salt) is a sodium salt form of the biologically active enantiomer of vitamin B5 and is used in the synthesis of coenzyme A. The L-form of pantothenic acid is biologically inactive and has been shown to act as an antagonist of D-pantothenic acid. Group: Biochemicals. Alternative Names: Calcium D-Pantothenate; N-[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]- β-alanine, Calcium salt. Grades: Cell Culture Grade. CAS No. 137-08-6. Pack Sizes: 100g, 250g, 500g, 1Kg. Molecular Formula: C18H32N2O10 Ca, Molecular Weight: 476.54. US Biological Life Sciences. | Worldwide |
| D-Pantothenic acid calcium salt hydrate | D-Pantothenic acid calcium salt hydrate. Group: other glass and ceramic materials. CAS No. 331748-07-3. Product ID: calcium; 3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoate; hydrate. Molecular formula: 494.5g/mol. Mole weight: C18H34CaN2O11. CC(C)(CO)C(C(=O)NCCC(=O)[O-])O. CC(C)(CO)C(C(=O)NCCC(=O)[O-])O. O. [Ca+2]. InChI=1S/2C9H17NO5.Ca.H2O/c2*1-9(2, 5-11)7(14)8(15)10-4-3-6(12)13; ; /h2*7, 11, 14H, 3-5H2, 1-2H3, (H, 10, 15)(H, 12, 13); ; 1H2/q; ; +2; /p-2/t2*7-; ; /m00./s1. KUKRZUPDYACRAM-GXIDORRSSA-L. |  |
| D-Pantothenic acid hemicalcium salt | D-Pantothenic acid hemicalcium salt is an orally active vitamin that reduces patulin in apple juice. D-Pantothenic acid hemicalcium salt removes ROS. D-Pantothenic acid hemicalcium salt has antibacterial and immunomodulatory activities. D-Pantothenic acid hemicalcium salt also has the effect of improving osteoporosis and obesity[1][2][3][4][5][6][7][8]. Uses: Scientific research. Group: Natural products. Alternative Names: Calcium pantothenate; Calcium D-pantothenate; Vitamin B5 calcium salt. CAS No. 137-08-6. Pack Sizes: 10 mM * 1 mL; 500 mg; 5 g; 10 g; 25 g. Product ID: HY-N0681. | |
| D-Pantothenic acid sodium | D-Pantothenic acid sodium (Sodium pantothenate) is an essential trace nutrient that functions as the obligate precursor of coenzyme A (CoA). D-Pantothenic acid sodium plays key roles in myriad biological processes, including many that regulate carbohydrate, lipid, protein, and nucleic acid metabolism [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Sodium pantothenate; Vitamin B5 sodium. CAS No. 867-81-2. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0430A. | |
| D-Pantothenic acid sodium salt | 100g Pack Size. Group: Analytical Reagents, Biochemicals, Organics. Formula: C9H16NO5 ¢Na. CAS No. 867-81-2. Prepack ID 38950533-100g. Molecular Weight 241.22. See USA prepack pricing. | |
| D-Pantothenic Acid Sodium Salt | D-Pantothenic acid sodium is a sodium salt form of the biologically active enantiomer of pantothenic acid, which is a precursor in the biosynthesis of coenzyme A. It is a water-soluble vitamin and an essential nutrient for for many animals. It is used to synthesize coenzyme-A (CoA) and synthesize and metabolize proteins, carbohydrates, and fats by animals. Uses: D-pantothenic acid sodium is an essential nutrient for for many animals. it is used to synthesize coenzyme-a (coa) and synthesize and metabolize proteins, carbohydrates, and fats by animals. Synonyms: Sodium D-pantothenate; N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-,monosodiumsalt,(R)-.beta.-Alanine; Sodium pantothenate; Vitamin B5 sodium; Sodium (R)-3-(2,4-dihydroxy-3,3-dimethylbutanamido)propanoate. Grade: 99%. CAS No. 867-81-2. Molecular formula: C9H16NNaO5. Mole weight: 241.22. | |
| D-Pantothenic Acid, Sodium Salt (Vitamin B5) | Pantothenic acid (vitamin B5) is a precursor in the biosynthesis of coenzyme A, which is an essential cofactor functioning as an acyl group carrier and carbonyl-activating group for the citric acid cycle and fatty acid metabolism. Two enantiomers of pantothenic acid exist, D- or L-form. D-Pantothenic acid (sodium salt) is a sodium salt form of the biologically active enantiomer of vitamin B5 and is used in the synthesis of coenzyme A. The L-form of pantothenic acid is biologically inactive and has been shown to act as an antagonist of D-pantothenic acid. Group: Biochemicals. Alternative Names: Sodium D-Pantothenate; N-[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]- β-alanine, monosodium salt. Grades: Cell Culture Grade. CAS No. 867-81-2. Pack Sizes: 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| (2R)-2-hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-4-phenylbutyl)butanamide | (2R)-2-hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-4-phenylbutyl)butanamide or RR6 is an inhibitor of Vanin which is an enzyme that play a role in the recycling of pantothenic acid (vitamin B5) from pantetheine. Alterations in plasma lipid concentrations in rats caused by RR6 indicates its potential usefulness. Group: Biochemicals. Grades: Highly Purified. CAS No. 1351758-37-6. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C16H23NO4, Molecular Weight: 293.36. US Biological Life Sciences. | Worldwide |
| (2R)-2-hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-4-phenylbutyl)butanamide-d5 | (2R)-2-hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-4-phenylbutyl)butanamide-d5 or RR6 (vanin inhibitor)-d5 is the labelled analogue of 2R)-2-hydroxy-3-(hydroxymethyl)-3-methyl-N-(3-oxo-4-phenylbutyl)butanamide or RR6 (vanin inhibitor) which is an enzyme that play a role in the recycling of pantothenic acid (vitamin B5) from pantetheine. Alterations in plasma lipid concentrations in rats caused by RR6 indicates its potential usefulness. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C16H18D5NO4, Molecular Weight: 298.39. US Biological Life Sciences. | Worldwide |
| 3-Methyl-2-oxobutanoic acid | 3-Methyl-2-oxobutanoic acid is a precursor of pantothenic acid in Escherichia coli. Uses: Scientific research. Group: Natural products. CAS No. 759-05-7. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-W006057. | |
| 3-Methyl-2-oxobutanoic acid (Standard) | 3-Methyl-2-oxobutanoic acid (Standard) is the analytical standard of 3-Methyl-2-oxobutanoic acid. This product is intended for research and analytical applications. 3-Methyl-2-oxobutanoic acid is a precursor of pantothenic acid in Escherichia coli. Uses: Scientific research. Group: Natural products. CAS No. 759-05-7. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-W006057R. | |
| β-Alanine | β-Alanine is a naturally occurring beta amino acid, formed in vivo by the degradation of dihydrouracil and carnosine. It is a component of pantothenic acid and the rate-limiting amino acid in the biosynthesis of the histidinyl antioxidant dipeptides carnosine and anserine. It is a non-specific endogenous agonist at the inhibitory glycine receptor and more selective than taurine. It is the rate-limiting precursor of carnosine, as a result supplementation with β-alanine increases the concentration of carnosine in muscles. It has been used as a ligand for the orphan MAS-related receptor. It is also applied in culture media used for certain strains of yeast to test for β-alanine auxotrophy. It also distinguishes between GABA transporters. Nutritional supplement in health care products. Uses: Β-alanine is a non-essential amino acid that is critical for the creation of new drugs. it is an essential component in many pharmacological research and application fields due to its distinct qualities and possible therapeutic advantages. the synthesis of carnosine, a dipeptide made of β-alanine and histidine, is one of the primary functions of β-alanine in drug discovery. carnosine has been rese. Synonyms: 2-Carboxyethylamine; 3-Aminopropanoic Acid; 3-Aminopropionic Acid; Abufene; NSC 7603; β-Aminopropanoic Acid; β-Aminopropionic Acid; ω-Aminopropionic Acid. Grade: 98%. CAS No. 107-95-9. Mole | |
| Calcium D-(+)-pantothenate | Calcium D-(+)-pantothenate is a precursor for coenzyme A biosynthesis. Applications: A precursor for coenzyme a biosynthesis. Group: Coenzymes. Synonyms: D-Pantothenic acid calcium salt; Vitamin B5. CAS No. 137-08-6. Mole weight: 476.53. Appearance: Powder. Form: Solid. D-Pantothenic acid calcium salt; Vitamin B5; Calcium D-(+)-pantothenate; 137-08-6. Cat No: COEC-019. |  |
| Calcium pantothenate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardseuropean pharmacopoeia (ph. eur.)impurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Calcium D-pantothenate, Vitamin B5 calcium salt, Pantholin, Panthoject, Calcium D-(+)-N-(alpha,gamma-dihydroxy-beta,beta-dimethylbutyryl)-beta-alaninate, N-(2,4-Dihydroxy-3,3-dimethylbutyryl)-beta-alanine calcium, Calpan, beta-Alanine, N-[(2R)-2,4-dihydroxy-3,3-dimethyl-1-oxobutyl]-, calcium salt (2:1), Pancal, Pantothenate calcium, Calpanate, Calcium, bis(pantothenato)- (7CI), NSC 36292, Dextro calcium pantothenate, beta-Alanine, N-(2,4-dihydroxy-3,3-dimethyl-1-oxobutyl)-, calcium salt (2:1), (R)-, Pantothenic acid hemicalcium salt, Calcium D-(+)-pantothenate, Panthothenic acid hemicalcium salt, SKF-D-58861X, Calcium pantothenate, Pantothenic acid calcium salt, Pantothenic acid, calcium salt (2:1), D- (8CI), (+)-Pantothenic acid calcium salt,Calcium bis[3-[[(2R)-2,4-dihydroxy-3,3-dimethylbutanoyl]amino]propanoate]. |  |
| Calcium pantothenate EP Impurity H | An impurity of Calcium pantothenate. Calcium pantothenate is a water-soluble vitamin B5 derivative used as a dietary supplement and additive in food, feed, and cosmetics. Synonyms: 3-[(5Ξ)-5-(1-hydroxy-2-methylpropan-2-yl)-4-oxo-1,3-oxazolidin-3-yl]propanoic acid; Pantothenic Acid EP Impurity H; Calcium pantothenate Impurity H; Pantothenic Acid Impurity H. Molecular formula: C10H17NO5. Mole weight: 231.25. | |
| Dexpanthenol | D-Panthenol is an analogue of pantothenic acid, a member of the B complex vitamins. D-Panthenol is the biologically active enantiomer of Panthenol. Group: Biochemicals. Grades: Highly Purified. CAS No. 81-13-0. Pack Sizes: 100g, 250g, 500g. Molecular Formula: C9H19NO4, Molecular Weight: 205.25. US Biological Life Sciences. | Worldwide |
| D-Panthenol | D-Panthenol is an analogue of pantothenic acid, a member of the B complex vitamins. D-Panthenol is the biologically active enantiomer of Panthenol. Group: Biochemicals. Grades: Highly Purified. CAS No. 81-13-0. Pack Sizes: 10g, 50g, 100g, 250g, 500g. Molecular Formula: C9H19NO4, Molecular Weight: 205.25. US Biological Life Sciences. | Worldwide |
| D-Panthenol | D-Panthenol is the biologically-active alcohol of pantothenic acid, which leads to an elevation in the amount of coenzyme A in the cell. D-panthenol exhibits nephroprotective effect in AKI, promotes tissue repair and regeneration. Uses: Scientific research. Group: Natural products. Alternative Names: Dexpanthenol. CAS No. 81-13-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1391. | |
| D-Panthenol (Standard) | D-Panthenol (Standard) is the analytical standard of D-Panthenol. This product is intended for research and analytical applications. D-Panthenol is the biologically-active alcohol of pantothenic acid, which leads to an elevation in the amount of coenzyme A in the cell. D-panthenol exhibits nephroprotective effect in AKI, promotes tissue repair and regeneration. Uses: Scientific research. Group: Natural products. CAS No. 81-13-0. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1391R. | |
| D-(-)-Pantolactone | D-(-)-Pantolactone is a chiral auxiliary used in many asymmetric synthesis reactions. It is also an important intermediate in the synthesis of pantothenic acid and a degradation product of pantothneic acid in the liver. Synonyms: (3R)-Dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone; (-)-(R)-Pantolactone; (-)-2-Hydroxy-3,3-dimethyl-γ-butyrolactone; (-)-Pantoyl Lactone; (3R)-Tetrahydro-3-hydroxy-4,4-dimethylfuran-2-one; Pantothenic Lactone; D-(-)-α-Hydroxy-β,β-dimethyl-γ-butyrolactone; (R)-α-Hydroxy-β,β-dimethyl-γ-butyrolactone; Pantolactone; (R)-pantolactone; (R)-3-hydroxy-4,4-dimethyldihydrofuran-2(3H)-one. Grade: ≥ 95 %. CAS No. 599-04-2. Molecular formula: C6H10O3. Mole weight: 130.14. | |
| pantothenate kinase | Pantothenate kinase (EC 2.7.1.33, PanK; CoaA) is the first enzyme in the Coenzyme A biosynthetic pathway. It phosphorylates pantothenate (vitamin B5) to form 4'-phosphopantothenate at the expense of a molecule of adenosine triphosphate (ATP). It is the rate-limiting step in the biosynthesis of CoA. Group: Enzymes. Synonyms: pantothenate kinase (phosphorylating); pantothenic acid kinase; ATP:pantothenate 4'-phosphotransferase; D-pantothenate kinase. Enzyme Commission Number: EC 2.7.1.33. CAS No. 9026-48-6. 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-3064; pantothenate kinase; EC 2.7.1.33; 9026-48-6; pantothenate kinase (phosphorylating); pantothenic acid kinase; ATP:pantothenate 4'-phosphotransferase; D-pantothenate kinase. Cat No: EXWM-3064. | |
| phosphopantothenoylcysteine decarboxylase | This enzyme belongs to the family of lyases, to be specific the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in coenzyme A (CoA) biosynthesis from pantothenic acid. Group: Enzymes. Synonyms: 4-phosphopantotheoylcysteine decarboxylase; 4-phosphopantothenoyl-L-cysteine decarboxylase; PPC-decarboxylase; N-[(R)-4'-phosphopantothenoyl]-L-cysteine carboxy-lyase. Enzyme Commission Number: EC 4.1.1.36. CAS No. 9024-69-5. 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-4780; phosphopantothenoylcysteine decarboxylase; EC 4.1.1.36; 9024-69-5; 4-phosphopantotheoylcysteine decarboxylase; 4-phosphopantothenoyl-L-cysteine decarboxylase; PPC-decarboxylase; N-[(R)-4'-phosphopantothenoyl]-L-cysteine carboxy-lyase. Cat No: EXWM-4780. | |
| (RS)-Pantoic Acid Sodium Salt | (RS)-Pantoic acid is formed by bacterial degradation of Pantothenic acid. (RS)-Pantoic acid is an impurity of Pantothenic acid. Group: Biochemicals. Alternative Names: 2,4-Dihydroxy-3,3-dimethylbutanoic Acid Sodium Salt; DL-2,4-Dihydroxy-3,3-dimethylbutyric Acid Monosodium Salt; α,γ-Dihydroxy- β, β-dimethylbutyric Acid Sodium Salt; (±)-Pantoic Acid Sodium Salt; DL-Pantoic Acid Sodium Salt; NSC 28026. Grades: Highly Purified. CAS No. 1902-1-8. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Sodium 3-methyl-2-oxobutanoate | Sodium 3-methyl-2-oxobutanoate is a precursor of pantothenic acid in Escherichia coli[1][2][3]. Uses: Scientific research. Group: Natural products. CAS No. 3715-29-5. Pack Sizes: 500 mg; 1 g. Product ID: HY-W006057A. | |
| 2-dehydropantoate 2-reductase | This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (R)-pantoate:NADP+ 2-oxidoreductase. Other names in common use include 2-oxopantoate reductase, 2-ketopantoate reductase, 2-ketopantoic acid reductase, ketopantoate reductase, and ketopantoic acid reductase. This enzyme participates in pantothenate and coa biosynthesis. Group: Enzymes. Synonyms: 2-oxopantoate reductase; 2-ketopantoate reductase; 2-ketopantoic acid reductase; ketopantoate reductase; ketopantoic acid reductase. Enzyme Commission Number: EC 1.1.1.169. CAS No. 37211-74-8. 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-0072; 2-dehydropantoate 2-reductase; EC 1.1.1.169; 37211-74-8; 2-oxopantoate reductase; 2-ketopantoate reductase; 2-ketopantoic acid reductase; ketopantoate reductase; ketopantoic acid reductase. Cat No: EXWM-0072. | |
| 3-(2,2,5,5-Tetramethyl-1,3-dioxane-4-carboxamido)propanoic acid | An impurity of Calcium pantothenate. Calcium pantothenate is a water-soluble vitamin B5 derivative used as a dietary supplement and additive in food, feed, and cosmetics. Synonyms: 3-[N-(2,2,5,5-Tetramethyl-1,3-dioxane-4-carbonyl)amino]propionic acid; N-[(2,2,5,5-Tetramethyl-1,3-dioxan-4-yl)carbonyl]-β-alanine. Grade: ≥95%. CAS No. 135422-90-1. Molecular formula: C12H21NO5. Mole weight: 259.30. | |
| β-Alanine | Acrylonitrile reacts with ammonia in diphenylamine and tert-butanol solution to form β-aminopropanitrile, which is obtained by alkaline hydrolysis. Synonyms: BETA-ALA;BETA-ALANINE;BETA-AMINO-PROPIONIC ACID;H-GLY(C*CH2)-OH;H-BETA-ALA-OH;FEMA 3252;RARECHEM EM WB 0001;NH2-(CH2)2-COOH. CAS No. 107-95-9. Product ID: PAP-0033. Molecular formula: C3H7NO2. Category: Amino acid. Product Keywords: Amino Acid Series; β-Alanine; PAP-0033; Amino acid; C3H7NO2; 107-95-9. Appearance: Crystalline Powder. Chemical Name: β-Alanine. Grade: Pharmaceutical Grade. Solubility: Practically insoluble in methanol, ethanol, ether, benzene. Soluble in acids and alkalies. Storage: Keep in dark place,Inert atmosphere,Room temperature. Applications: This product is mainly used for the synthesis of medicine and feed additives calcium pantothenate raw materials, can also be used for electroplating corrosion inhibitors, as biological reagents and organic synthesis intermediates. Used as food, health additives. Boiling Point: 244.01°C (rough estimate). Melting Point: 235 °C (dec.) (lit.). Density: 1,543g/cm. Product Description: Acrylonitrile reacts with ammonia in diphenylamine and tert-butanol solution to form β-aminopropanitrile, which is obtained by alkaline hydrolysis. | |
| 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}. CAS No. 85-61-0. Molecular formula: C21H36N7O16P3S. Mole weight: 767.53. | |
| 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. | |
| dihydroxy-acid dehydratase | This enzyme participates in valine, leucine and isoleucine biosynthesis and pantothenate and coenzyme A (CoA) biosynthesis. Group: Enzymes. Synonyms: acetohydroxyacid dehydratase; α,β-dihydroxyacid dehydratase; 2,3-dihydroxyisovalerate dehydratase; α,β-dihydroxyisovalerate dehydratase; dihydroxy acid dehydrase; DHAD; 2,3-dihydroxy-acid hydro-lyase. Enzyme Commission Number: EC 4.2.1.9. CAS No. 9024-32-2. 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-5073; dihydroxy-acid dehydratase; EC 4.2.1.9; 9024-32-2; acetohydroxyacid dehydratase; α,β-dihydroxyacid dehydratase; 2,3-dihydroxyisovalerate dehydratase; α,β-dihydroxyisovalerate dehydratase; dihydroxy acid dehydrase; DHAD; 2,3-dihydroxy-acid hydro-lyase. Cat No: EXWM-5073. | |
| DL-Panthenol | DL-Panthenol (DL-Pantothenol) is an alcohol derivative of pantothenyl acid. DL-Panthenol exerts eyelash protection effect. DL-Panthenol is widely used in the Skin and hair conditioner research [1] [2]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: DL-Pantothenol; DL-Pantothenyl alcohol. CAS No. 16485-10-2. Pack Sizes: 10 mM * 1 mL; 25 g. Product ID: HY-B1024. | |
| FUSIDIC ACID | Fusidic acid is a steroid antibiotic that is isolated from the fermentation broth of Fusidium coccineum. It has a role as a protein synthesis inhibitor, an EC 2.7.1.33 (pantothenate kinase) inhibitor and an Escherichia coli metabolite. It is a 3alpha-hydroxy steroid, an 11alpha-hydroxy steroid, a sterol ester, a steroid acid, an alpha,beta-unsaturated monocarboxylic acid and a steroid antibiotic. It is a conjugate acid of a fusidate. It derives from a hydride of a 5alpha-cholestane. CAS No. 6990-6-3. Product ID: PAP-0038. Molecular formula: C31H48O6. Category: Antibacterial, anti-inflammatory and antiviral. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; FUSIDIC ACID; PAP-0038; Antibacterial, anti-inflammatory and antiviral; C31H48O6; 6990-06-3. Standard: EP/ BP. Color: White to Off-White. EC Number: 230-256-0. Physical State: neat. Solubility: Practically insoluble in water, freely soluble in ethanol (96 per cent). Storage: Sealed in dry,2-8°C. Applications: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. Boiling Point: 521.49°C (rough estimate). Melting Point: 190-192°C. Density: 1.0389 (rough estimate). Product Description: Fusidic acid is an antibiotic that is often used topically in creams or ointments and eyedrops but may also be given systemically as tablets or injections. | |
| Native Crotalus adamanteus venom Pyrophosphatase, Nucleotide | In enzymology, a nucleotide diphosphatase (EC 3.6.1.9) is an enzyme that catalyzes the chemical reaction:a dinucleotide + H2O<-> 2 mononucleotides. Thus, the two substrates of this enzyme are dinucleotide and H2O, whereas its product is mononucleotide. This enzyme belongs to the family of hydrolases, specifically those acting on acid anhydrides in phosphorus-containing anhydrides. This enzyme participates in 5 metabolic pathways:purine metabolism, starch and sucrose metabolism, riboflavin metabolism, nicotinate and nicotinamide metabolism, and pantothenate and coa biosynthesis. Group: Enzymes. Synonyms: nucleotide diphosphatase; EC 3.6.1.9; nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; 9032-64-8. Enzyme Commission Number: EC 3.6.1.9. CAS No. 9032-64-8. Nucleotide Pyrophosphatase. Activity: 4-8 units/mg protein, vial of ~25 units. Storage: -20°C. Form: Lyophilized powder containing approx. 35% Tris buffer salts. Source: Crotalus adamanteus venom. nucleotide diphosphatase; EC 3.6.1.9; nucleotide pyrophosphatase; nucleotide-sugar pyrophosphatase; 9032-64-8. Pack: vial of ~25 units. Cat No: NATE-0493. | |
| Native Yeast Coenzyme A, Trilithium Salt | 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, Trilithium Salt; CoA-Li; 18439-24-2. CAS No. 18439-24-2. Purity: Determined by enzyme analysis with PTA* (> 75%) *PTA = Phosphotrasacetylase (LM) (EC 2.3.1.8.). CoA. Mole weight: 685.41. Storage: Keep tightly stoppered in the dark below 5°C. For Prolonged storage, keep below-20°C. Source: Yeast. Coenzyme A, Trilithium Salt; CoA-Li; 18439-24-2. Cat No: NATE-0146. | |
| pantoate-β-alanine ligase (AMP-forming) | This enzyme belongs to the family of ligases, specifically those forming carbon-nitrogen bonds as acid-D-amino-acid ligases (peptide synthases). This enzyme participates in beta-alanine metabolism and pantothenate and CoA biosynthesis. Group: Enzymes. Synonyms: pantothenate synthetase; pantoate activating enzyme; pantoic-activating enzyme; D-pantoate:β-alanine ligase (AMP-forming); pantoate-β-alanine ligase (ambiguous). Enzyme Commission Number: EC 6.3.2.1. CAS No. 9023-49-8. 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-5730; pantoate-β-alanine ligase (AMP-forming); EC 6.3.2.1; 9023-49-8; pantothenate synthetase; pantoate activating enzyme; pantoic-activating enzyme; D-pantoate:β-alanine ligase (AMP-forming); pantoate-β-alanine ligase (ambiguous). Cat No: EXWM-5730. | |
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