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| Product | Description | |
|---|---|---|
| Codeine Phosphate Impurity 1 | Codeine Phosphate Impurity 1. Uses: For analytical and research use. Molecular formula: C35H38N2O6. Mole weight: 582.7. Catalog: APB11497. |  |
| Codeinone | Codeinone. Group: Biochemicals. Alternative Names: (5a)-7,8-Didehydro-4,5-epoxy-3-methoxy-17-methyl-morphinan-6-one; 7,8-Didehydro-4,5a-epoxy-3-methoxy-17-methyl-morphinan-6-one; (-)-Codeinone. Grades: Highly Purified. CAS No. 467-13-0. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C18H19NO3. US Biological Life Sciences. |  Worldwide |
| codeinone reductase (NADPH) | Catalyses the reversible reduction of codeinone to codeine, which is a direct precursor of morphine in the opium poppy plant, Papaver somniferum. Group: Enzymes. Enzyme Commission Number: EC 1.1.1.247. CAS No. 153302-41-1. 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-0153; codeinone reductase (NADPH); EC 1.1.1.247; 153302-41-1. Cat No: EXWM-0153. |  |
| Codergocrine mesilate | Codergocrine mesilate is a mixture of the methanesulfonate salts of three dihydrogenated ergot alkaloids. It binds with high affinity to the GABAA receptor Cl- channel, producing an allosteric interaction with the benzodiazepine site. It also interacts with central dopaminergic, serotonergic and adrenergic (α1) receptors. It displays antiproliferative activity and cognition-enhancing, anticonvulsant and sedative activity in vivo. It has been used to treat dementia and age-related cognitive impairment, such as in Alzheimer disease, as well as to aid in recovery after stroke. It may be used in conjunction with other cerebral enhancers like piracetam, with which it may act synergistically. It was developed by Albert Hofmann for Sandoz (now part of Novartis). Uses: Codergocrine mesilate displays antiproliferative activity and cognition-enhancing, anticonvulsant and sedative activity in vivo. it has been used to treat dementia and age-related cognitive impairment, such as in alzheimer disease, as well as to aid in recovery after stroke. it may be used in conjunction with other cerebral enhancers like piracetam, with which it may act synergistically. Synonyms: CCK 179, CCK-179, CCK179; Dihydroergotoxine mesylate; Dihydroergotoxine methanesulfonate; Dihydroergotoxine methanesulphonate; Dihydroergotoxine monomethanesulfonate(salt); Ergoloid mesylates. Grade: 95%. CAS No. 8067-24-1. Molecular formula: C20H29N3O5S. Mole |  |
| Cod Liver Oil 2500A/250D Deodorized | Cod Liver Oil 2500A/250D Deodorized. |  CA, FL & NJ |
| Co/DOBDC | Revolutionize your Metal-organic Frameworks (MOFs) Materials research with Co/DOBDC from CD Bioparticles. Group: Cobalt-based mofs (co-mof). |  |
| Codonopsi Powder | Codonopsi Powder. | CA, FL & NJ |
| Co-doped Nb2CTx Multilayer Mxene | Co-doped Nb2CTx Multilayer Mxene. Purity: 99%, Co doping amount 1%. |  |
| Co-doped Ti2CTx Multilayer Mxene | Co-doped Ti2CTx Multilayer Mxene. Purity: 99%, Co doping amount 1%. | |
| Co-doped Ti3C2Tx Multilayer Mxene | Co-doped Ti3C2Tx Multilayer Mxene. Purity: 99%, Co doping amount 1%. | |
| Codrituzumab | Codrituzumab (GC33) is a humanized monoclonal antibody targeting human GPC3 (glypican-3), with high affinity (Kd of 0.673 nM). GPC3 is an oncofetal protein expressed on the cell surface of hepatocellular carcinoma (HCC). Codrituzumab induces antibody-dependent cellular cytotoxicity (ADCC) and inhibits tumor growth[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GC33; RO5137382. CAS No. 1365267-33-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99013. |  |
| Codrituzumab | Codrituzumab is a humanized monoclonal antibody against Glypican-3 (GPC3). Codrituzumab binds to GPC3 and suppresses GPC3-expressing tumor cell growth. Synonyms: GC33; RO5137382. CAS No. 1365267-33-9. | |
| Coelenteramine 400a | Coelenteramine 400a (Coelenterazine 400a), a derivative of Coelenterazine, is a Renilla luciferase (RLuc) substrate. In the presence of Coelenteramine 400a, RLuc can emit blue light at 395 nm[1][2]. Coelenterazine 400a will causes color change in the bioluminescence reaction of Rluc by replacing the sulfur and oxygen heteroatoms of the methylene bridge. Coelenterazine 400a provides higher signal resolution and can be used in the research of bioluminescence resonance energy transfer (BRET)[3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Coelenterazine 400a; Bisdeoxycoelenterazine. CAS No. 70217-82-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118462. | |
| Coelenterazine | Coelenterazine. Uses: For analytical and research use. Alternative Names: Oplophorus luciferin. CAS No. 55779-48-1. Molecular formula: C26H21N3O3. Mole weight: 423.46. Purity: ≥95%. IUPAC Name: 8-benzyl-6-(4-hydroxyphenyl)-2-[(4-hydroxyphenyl)methyl]imidazo[1,2-a]pyrazin-3-ol. Catalog: APB55779481. | |
| Coelenterazine | Coelenterazine is a luciferin, a light-emitting biomolecule that serves as a substrate for luciferases or as a constituent of photoproteins, including aequorin.1 The oxidation of coelenterazine to coelenteramide is accompanied by emission of blue light (emission maximum, 460-470 nm). Luciferase-mediated oxidation of coelenterazine or a derivative is used as an energy donor, typically to a form of green or yellow fluorescent protein, in bioluminescent resonance energy transfer studies.2,3 Alternatively, the calcium-mediated release of coelenterazine from aequorin, followed by non-enzymatic oxidation of this compound, results in bioluminescence. As light emission depends on both calcium and cellular redox status, this reaction is used to non-fluorescently detect changes in calcium level and redox status.4,5. Group: Biochemicals. Alternative Names: 3,2-Dihydro-2-(p-hydroxybenzyl)-6-(p-hydroxyphenyl)-8-benzylimidazolo[1,2-a]pyrazin-3-one; CLZN; Preluciferin; Luciferin; 6-(4-hydroxyphenyl)-2-[(4-hydroxyphenyl)methyl]-8-(phenylmethyl)-imidazo[1,2-a]pyrazin-3(7H)-one. Grades: Highly Purified. CAS No. 55779-48-1. Pack Sizes: 5mg, 10mg, 25mg. Molecular Formula: C??H??N?O?, Molecular Weight: 423.46. US Biological Life Sciences. | Worldwide |
| Coelenterazine | Coelenterazine Inhibitor. Uses: Scientific use. Product Category: T6808. CAS No. 55779-48-1. |  |
| Coelenterazine | Coelenterazine is a luminescent enzyme substrate for apoaequorin and Renilla luciferase. Renilla luciferase and substrate coelenterazine has been used as the bioluminescence donor in bioluminescence resonance energy transfer (BRET) to detect protein-protein interactions. Coelenterazine is a superoxide anion-sensitive chemiluminescent probe and it can also be used in chemiluminescent detection of peroxynitrite (Ex/Em = 429/466 nm)[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 55779-48-1. Pack Sizes: 500 μg; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-18743. | |
| Coelenterazine 400a | Coelenterazine 400 a is a chromophore that produces the chemiluminescence displayed by the Aequorin protein in the presence of Ca2+. Group: Biochemicals. Alternative Names: 6-Phenyl-2, 8-bis (phenylmethyl) imidazo[1, 2-a]pyrazin-3 (7H) -one; Bisdeoxycoelenterazine ; Coelenterazine HH; DeepBlueC; Dideoxycoelenterazine; BlueSyn C; 2,8-Dibenzyl-6-phenyl-imidazo[1,2a]pyrazin-3-(7H)-one. Grades: Highly Purified. CAS No. 70217-82-2. Pack Sizes: 5mg, 10mg. Molecular Formula: C??H??N?O, Molecular Weight: 391.46. US Biological Life Sciences. | Worldwide |
| Coelenterazine e | Coelenterazine e. Group: Biochemicals. Grades: Highly Purified. CAS No. 114496-02-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 20mg. Molecular Formula: C28H23N3O3, Molecular Weight: 449.5. US Biological Life Sciences. | Worldwide |
| Coelenterazine F | Coelenterazine F. Group: Biochemicals. Alternative Names: Coelenterazine-Fluoride; 8-benzyl-2- (4-fluorobenzyl) -6- (4-hydroxyphenyl) imidazo[1, 2- a]pyrazin-3(7H)-one. Grades: Highly Purified. CAS No. 123437-16-1. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 20mg. Molecular Formula: C26H20FN3O2. US Biological Life Sciences. | Worldwide |
| Coelenterazine h | Coelenterazine h. Group: Biochemicals. Alternative Names: 2-Deoxycoelenterazine; 2, 8-dibenzyl-6- (4-hydroxyphenyl) imidazo[1, 2-a]pyrazin-3 (7H) -one. Grades: Highly Purified. CAS No. 50909-86-9. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 20mg. Molecular Formula: C26H21N3O2. US Biological Life Sciences. | Worldwide |
| Coelenterazine h | Coelenterazine h (2-Deoxycoelenterazine), a coelenterazine derivative, is a luminescent substrate for RLuc8. Coelenterazine h is more sensitive to Ca2+, thus providing a valuable tool for measuring small changes in Ca2+ concentrations (Ex/Em = 437/466 nm)[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 2-Deoxycoelenterazine; CLZN-h. CAS No. 50909-86-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-D1024. | |
| Coelenterazine v | Coelenterazine v. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 20mg. US Biological Life Sciences. | Worldwide |
| Coenzyme A | Coenzyme A. CAS No: 85-61-0 |  Sarchem Laboratories New Jersey NJ |
| 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 | 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. Category: Signaling pathways. CAS No. 85-61-0. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-128851. | |
| 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 hydrate | Coenzyme A hydrate. Uses: For analytical and research use. CAS No. 85-61-0 (anhydrous). Mole weight: 767.53 (anhydrous basis). Catalog: ALP85610. | |
| Coenzyme A, oxidized lithium salt | Coenzyme A, oxidized lithium salt. Uses: For analytical and research use. CAS No. 31664-36-5 (free acid). Mole weight: 1533.05 (free acid basis). Catalog: ALP31664365. | |
| Coenzyme A, S-(2E)-2-butenoate, tetralithium salt | Coenzyme A, S-(2E)-2-butenoate, tetralithium salt. Synonyms: Coenzyme A, S-2-butenoate, tetralithium salt, (E)-. CAS No. 102680-35-3. Molecular formula: C25H36N7O17P3S.4Li. Mole weight: 859.34. | |
| 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,s-(9Z,12Z)-9,12-octadecadienoate | Coenzyme a,s-(9Z,12Z)-9,12-octadecadienoate. CAS No. 6709-57-5. Product ID: ACM6709575-1. Molecular formula: C39H66N7O17P3S. Mole weight: 1029.96. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Coenzyme a,s-hexadecanoate | Coenzyme a,s-hexadecanoate. Alternative Names: PALMITOYL COENZYME A, K SALT;PALMITOYL COENZYME A POTASSIUM SALT;N-HEXADECANOYL COENZYME A, POTASSIUM;N-HEXADECANOYL COENZYME A POTASSIUM SALT;S-palmitoylcoenzyme A;[5-(6-aminopurin-9-yl)-2-[[[[3-[2-(2-hexadecanoylsulfanylethylcarbamoyl)ethylcarbamoyl]-3. CAS No. 1763-10-6. Product ID: ACM1763106-1. Molecular formula: C37H66N7O17P3S. Mole weight: 1044.03. Alfa Chemistry - ISO 9001:32057 Certified. | |
| 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. Category: Signaling pathways. CAS No. 55672-92-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 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 hydrate | Coenzyme A sodium salt hydrate. Uses: For analytical and research use. CAS No. 55672-92-9 (anhydrous). Mole weight: 767.53 (anhydrous free acid basis). EC Number: 259-747-8. Catalog: ALP55672929. | |
| Coenzyme A S-Pyrazinecarboxylate-d3 | Coenzyme A S-Pyrazinecarboxylate-d3 is the isotope labelled analog of Coenzyme A S-Pyrazinecarboxylate, which is a derivative of Coenzyme A. Molecular formula: C26H35D3N9O17P3S. Mole weight: 876.63. | |
| 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. Category: Signaling pathways. CAS No. 18439-24-2. Pack Sizes: 10 mg; 25 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. Grade: 95%. CAS No. 18439-24-2. Molecular formula: C21H33Li3N7O16P3S. Mole weight: 785.33. | |
| Coenzyme A, Trilithium Salt - CAS 18439-24-2 | Coenzyme A, Trilithium Salt - CAS 18439-24-2. Uses: For analytical and research use. CAS No. 18439-24-2. Mole weight: 785.33. Catalog: AP18439242-A. | |
| Coenzyme B12 | Coenzyme B12. Alternative Names: 5'-Deoxyadenosylcobalamin Adenosylcobalamin Cobamamide. CAS No. 13870-90-1. Purity: >99.0%. Product ID: FFC-AR-13870901. Molecular formula: C72H100CoN18O17P. Mole weight: 1579.58. Alfa Chemistry - ISO 9001:32057 Certified. | |
| Coenzyme B12 | Coenzyme B12. Group: Coenzymes. Synonyms: 5'-Deoxyadenosylcobalamine; Adenosyl cobalamine; Cobamamide; DMBC coenzyme. CAS No. 13870-90-1. Purity: ≥97%. Mole weight: 1579.58. 5'-Deoxyadenosylcobalamine; Adenosyl cobalamine; Cobamamide; DMBC coenzyme; Coenzyme B12; 13870-90-1. Cat No: COEC-023. | |
| 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 FO | Coenzyme FO, a deazaflavin chromophore, acts as an important hydride acceptor/donor in the central methanogenic pathway[1][2]. Uses: Scientific research. Category: Induced disease models products. CAS No. 37333-48-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-136497. | |
| 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 PQQ Pyrroloquinoline Quinone Powder 99% HPLC | Pyrroloquinoline quinone (PQQ) is a small molecule quinone compound. Although it is relatively rare in plants and animals, its content in breast milk is relatively significant. The most striking function of PQQ is that it acts as a redox agent, which can effectively reduce harmful oxidants in the body. Its unique "charging" ability allows PQQ to maintain its active state after reacting with glutathione and circulating multiple times. PQQ can promote the proliferation and functional improvement of mitochondria. Mitochondria are the energy factories of cells, providing energy to cells by producing adenosine triphosphate (ATP) and playing a key role in regulating cell metabolism. In the activity of mitochondria, PQQ can also affect the biological clock of cells, which is associated with the aging process of cells and has a potential impact on skin aging. In addition, PQQ has a good binding ability to specific protein structures in cells, and its antioxidant activity mainly occurs near proteins. In contrast, other antioxidants such as carotenoids (such as β-carotene and astaxanthin) mainly play a role near the cell membrane. Their respective positioning and mechanism of action result in differences in the antioxidant effects in different areas of the cell. Therefore, in antioxidant defense, PQQ and carotenoids have a complementary and synergistic relationship. CAS No. 72909-34-3. Pro | |
| Coenzyme Q0 | Coenzyme Q0 (CoQ0) is a potent, oral active ubiquinone compound can be derived from Antrodia cinnamomea. Coenzyme Q0 induces apoptosis and autophagy, suppresses of HER-2/AKT/mTOR signaling to potentiate the apoptosis and autophagy mechanisms. Coenzyme Q0 regulates NFκB/AP-1 activation and enhances Nrf2 stabilization in attenuation of inflammation and redox imbalance. Coenzyme Q0 has anti-angiogenic activity through downregulation of MMP-9/NF-κB and upregulation of HO-1 signaling[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CoQ0. CAS No. 605-94-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 g; 5 g. Product ID: HY-W016412. | |
| Coenzyme Q1 | Coenzyme Q1. Uses: For analytical and research use. CAS No. 727-81-1. Mole weight: 250.29. Catalog: AP727811. | |
| Coenzyme Q10 | Coenzyme Q10. Synonyms: Q-10, Ubiquinone 50, Ubiquinone-10. CAS No. 303-98-0. Pack Sizes: 100, 500 mg in poly bottle. Product ID: CDC10-0087. Molecular formula: C59H90O4. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Coenzyme Q10; CDC10-0087; 303-98-0; C59H90O4; Q-10, Ubiquinone 50, Ubiquinone-10; 206-147-9; MFCD00042919; 303-98-0. Purity: ≥98% (HPLC). Color: Yellow to dark orange. EC Number: 206-147-9. Physical State: Powder. Solubility: Soluble in chloroform. Quality Level: 200. Storage: -20°C. Application: cell analysis. Boiling Point: 715.32°C (rough estimate). Melting Point: 49 °C. Density: 0.9145 g/mL(rough estimate). |  |
| Coenzyme Q10 | 1g Pack Size. Group: Biochemicals, Research Organics & Inorganics. Formula: C59H90O4. CAS No. 303-98-0. Prepack ID 27199124-1g. Molecular Weight 863.34. See USA prepack pricing. | |
| Coenzyme Q10 | Coenzyme Q10. Group: Biochemicals. Alternative Names: (all-E)-2-(3, 7, 11, 15, 19, 23, 27, 31, 35, 39-decamethyl-2, 6, 10, 14, 18, 22, 26, 30, 34, 38-tetracontadecaenyl)-5, 6-dimethoxy-3-methyl-2, 5-cyclohexadiene-1, 4-dione; Bio-quinone Q10; CoQ10. Grades: Highly Purified. CAS No. 303-98-0. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C59H90O4. US Biological Life Sciences. | Worldwide |
| Coenzyme Q10 | Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CoQ10; Ubiquinone-10; Ubidecarenone. CAS No. 303-98-0. Pack Sizes: 100 mg; 200 mg; 500 mg; 1 g; 5 g. Product ID: HY-N0111. | |
| Coenzyme Q10 | Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration. Coenzyme Q10 is widely found in the mitochondria of the whole body. It has a stronger antioxidant function than vitamin C and vitamin E, can effectively remove free radicals, and has good anti-aging, whitening, and moisturizing functions. It can be widely used in anti-aging and wrinkle-removing, whitening and lightening spots, moisturizing and moisturizing, firming and tenderizing skin, sunscreen repair products, and it is compatible with lotion cream formula, gel formula, and water formula. Uses: Ingredient of health care products. Synonyms: CoQ10; Ubiquinone-10; Ubidecarenone; COQ10; Vitamin Q; NSC 140665; (all-E)-2-(3,7,11,15,19,23,27,31,35,39-Decamethyl-2,6,10,14,18,22,26,30,34,38-tetracontadecaenyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione; Bio-Quinone Q10; Cosmesome Q 10; Ensorb; Kaneka Q10; Kudesan. Grade: ≥98%. CAS No. 303-98-0. Molecular formula: C59H90O4. Mole weight: 863.34. | |
| Coenzyme Q10 | Coenzyme Q10 is an electron transport chain component of the mitochondria, which assists proton and electron transfer across the inner mitochondrial membrane. Studies indicate that Coenzyme Q10 can protect human endothelial cells from oxidative damage by modulating the nitric oxide pathway. In addition, Coenzyme Q10 inhibits LDL oxidation, a major process in the development of atherosclerosis. Coenzyme Q10 is known to suppress the down regulation of NOS3 (endothelial nitric oxide synthase, eNOS) and up-regulation of NOS2 (inducible nitric oxide synthase, iNOS). As a result of its ability to bind Ca2+, Coenzyme Q10 can transport this cation across artificial biomimetic membranes. Applications: A mitochondrial transporter chain component. Group: Coenzymes. Synonyms: CoQ10; Ubidecarenone; Ubiquinone-10; Q-10. CAS No. 303-98-0. Purity: ≥98%. Mole weight: 863.34. Appearance: Powder. Form: Solid. CoQ10; Ubidecarenone; Ubiquinone-10; Q-10; Coenzyme Q10; 303-98-0. Cat No: COEC-013. | |
| Coenzyme Q 10 | Coenzyme Q 10. CAS No: 303-98-0 | Sarchem Laboratories New Jersey NJ |
| Coenzyme Q10-[d5] | Coenzyme Q10-[d5], is the labelled analogue of Coenzyme Q10. Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration. Synonyms: Coenzyme Q10 D5. Grade: > 95%. Molecular formula: C59H85O4D5. Mole weight: 868.4. | |
| Coenzyme Q10-[d6] | Coenzyme Q10-[d6] is the labelled analogue of Coenzyme Q10. Coenzyme Q10 (ubiquinone, ubidecarenone, coenzyme Q) is a component of the electron transport chain and participates in aerobic cellular respiration. Synonyms: Coenzyme Q10-d6; Bio-Quinone Q10-d6; CoQ10-d6; Cosmesome Q 10-d6; Ensorb-d6; Kaneka Q10-d6; Kudesan-d6; Li-Q-Sorb-d6. Grade: 95% by HPLC; 95% atom D. CAS No. 1331655-96-9. Molecular formula: C59H84D6O4. Mole weight: 869.4. | |
| Coenzyme Q10 EP Impurity A | Coenzyme Q10 EP Impurity A. Uses: For analytical and research use. Alternative Names: 2,3-dimethoxy-5-methylbenzene-1,4-diol. CAS No. 3066-90-8. Molecular formula: C9H12O4. Mole weight: 184.19. Catalog: APB3066908. | |
| Coenzyme Q10 EP Impurity B | Coenzyme Q10 EP Impurity B. Uses: For analytical and research use. Alternative Names: 2-((2E,6E,10E,14E,18E,22E)-3,7,11,15,19,23,27-heptamethyloctacosa-2,6,10,14,18,22,26-heptaen-1-yl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione. Molecular formula: C44H66O4. Mole weight: 658.50. Catalog: APB05036. | |
| Coenzyme Q10 EP Impurity C | Coenzyme Q10 EP Impurity C. Uses: For analytical and research use. Alternative Names: 2,3-dimethoxy-5-methyl-6-((2E,6E,10E,14E,18E,22E,26E)-3,7,11,15,19,23,27,31-octamethyldotriaconta-2,6,10,14,18,22,26,30-octaen-1-yl)cyclohexa-2,5-diene-1,4-dione. Molecular formula: C49H74O4. Mole weight: 726.56. Catalog: APB05035. | |
| Coenzyme Q10 EP Impurity D | Coenzyme Q10 EP Impurity D. Uses: For analytical and research use. Alternative Names: Ubidecarenone EP Impurity D; 2,3-dimethoxy-5-methyl-6-((2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-yl)cyclohexa-2,5-diene-1,4-dione. CAS No. 303-97-9. Molecular formula: C54H82O4. Mole weight: 794.62. Catalog: APB303979. | |
| Coenzyme Q10 EP Impurity E | Coenzyme Q10 EP Impurity E. Uses: For analytical and research use. Alternative Names: Ubidecarenone EP Impurity E; (RS)-7,8-dimethoxy-2,5-dimethyl-2-((3E,7E,11E,15E,19E,23E,27E,31E)-4,8,12,16,20,24,28,32,36-nonamethylheptatriaconta-3,7,11,15,19,23,27,31,35-nonaen-1-yl)-2H-chromen-6-ol. Molecular formula: C59H90O4. Mole weight: 862.68. Catalog: APB05034. | |
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