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| Product | Description | |
|---|---|---|
| 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. Group: Biochemical assay reagents. Alternative Names: CoQ0. CAS No. 605-94-7. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-W016412. |  |
| Coenzyme Q1 | ?95%. Group: Fluorescence/luminescence spectroscopy. |  |
| 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 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 Q10 | Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent. Uses: Scientific research. Group: Natural products. 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. 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 | 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 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-d9 (dimethoxy-d6, methyl-d3) | ?98 atom % D, ?97% (CP). Group: Fluorescence/luminescence spectroscopy. | |
| Coenzyme Q10 (Standard) | Coenzyme Q10 (Standard) is the analytical standard of Coenzyme Q10. This product is intended for research and analytical applications. Coenzyme Q10 is an essential cofactor of the electron transport chain and a potent antioxidant agent. Uses: Scientific research. Group: Natural products. CAS No. 303-98-0. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0111R. | |
| Coenzyme Q10 USP | Coenzyme Q10 USP. |  CA, FL & NJ |
| Coenzyme Q2 | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Coenzyme Q4 | ?90%. Group: Fluorescence/luminescence spectroscopy. | |
| Coenzyme Q4 | Coenzyme Q4 increases the fluorescence polarization of perylene incorporated into ubiquinone-depleted bilayer and mitochondrial vesicles prepared from mitochondrial phospholipids. Applications: A compound which increases the fluorescence polarization of perylene. Group: Coenzymes. CAS No. 4370-62-1. Purity: ≥90%. Mole weight: 454.64. Form: Liquid. Coenzyme Q4; 4370-62-1. Cat No: COEC-021. | |
| Coenzyme Q6 | Coenzyme Q6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1065-31-2. Molecular formula: C39H58O4. Mole weight: 590.89. Catalog: APB1065312. | |
| Coenzyme Q8 | Coenzyme Q8. Group: Biochemicals. Alternative Names: 2, 3-Dimethoxy-5-methyl-6-[(2E, 6E, 10E, 14E, 18E, 22E, 26E)-3, 7, 11, 15, 19, 23, 27, 31-octamethyl-2, 6, 10, 14, 18, 22, 26, 30-dotriacontaoctaenyl]-2, 5-cyclohexadiene-1, 4-dione; 2,3-Dimethoxy-5-methyl-6-(3,7,11,15,19,23,27,31-octamethyl-2,6,10,14,18,22,26,30-dotriacontaoctaenyl)-p-benzoquinone; Ubiquinone 40. Grades: Highly Purified. CAS No. 2394-68-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C49H74O4. US Biological Life Sciences. | Worldwide |
| Coenzyme q9 | Coenzyme Q9 (Ubiquinone Q9), the major form of ubiquinone in rodents, is an amphipathic molecular component of the electron transport chain that functions as an endogenous antioxidant. Coenzyme Q9 attenuates the diabetes-induced decreases in antioxidant defense mechanisms. Coenzyme Q9 improves left ventricular performance and reduces myocardial infarct size and cardiomyocyte apoptosis. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Coenzyme Q(sub 9); 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-nonaenyl]cyclohexa-2,5-diene-1,4-dione; Coenzyme Q9; All-Trans Coenzyme Q9; Q-9 Ubiquinone-45 Ubiquinone. Product Category: Inhibitors. CAS No. 303-97-9. Molecular formula: C54H82O4. Mole weight: 795.23. Purity: 0.96. IUPACName: 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-nonaenyl]cyclohexa-2,5-diene-1,4-dione. Canonical SMILES: CC1=C(C(=O)C(=C(C1=O)OC)OC)CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C. Density: 0.97 g/cm³. Product ID: ACM303979. Alfa Chemistry ISO 9001:2015 Certified. Categories: Coenzyme Q10. |  |
| Coenzyme Q9 | ?96.0% (HPLC). Group: Fluorescence/luminescence spectroscopybuilding blocks. Alternative Names: Coenzyme Q9, Ubidecarenone EP impurity D, 2,3-dimethoxy-5-methyl-6-(3,7,11,15,19,23,27,31,35-nonamethyl-2,6,10,14,18,22,26,30,34-hexatriacontanonaenyl)-p-Benzoquinone, CoQ9,Ubiquinone Q9, Ubiquinone 9, 2,3-dimethoxy-5-methyl-6-[(2E,6E,10E,14E,18E,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethyl-2,6,10,14,18,22,26,30,34-hexatriacontanonaen-1-yl]-2,5-Cyclohexadiene-1,4-dione, NSC 226993. | |
| Coenzyme Q9 | Coenzyme Q9. Group: Biochemicals. Alternative Names: (all-E)-2, 3-dimethoxy-5-methyl-6-(3, 7, 11, 15, 19, 23, 27, 31, 35-nonamethyl-2, 6, 10, 14, 18, 22, 26, 30, 34-hexatriacontanonaenyl)-2, 5-cyclohexadiene-1, 4-dione. Grades: Highly Purified. CAS No. 303-97-9. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. Molecular Formula: C54H82O4. US Biological Life Sciences. | Worldwide |
| Coenzyme Q9 | Coenzyme Q9 is a co-enzyme that is lipid solumbe compononet of cell membranes. It is useful in electron and proton transport of liposome systems. It is also a useful tool in vitro to increase the life span of cells. Applications: A useful tool in vitro to increase the life span of cells. Group: Coenzymes. Synonyms: Ubiquinone-9. CAS No. 303-97-9. Purity: ≥98%. Mole weight: 795.23. Form: Solid. Ubiquinone-9; Coenzyme Q9; 303-97-9. Cat No: COEC-045. | |
| Coenzyme Q9 | Coenzyme Q9 (Ubiquinone Q9), the major form of ubiquinone in rodents, is an amphipathic molecular component of the electron transport chain that functions as an endogenous antioxidant. Coenzyme Q9 attenuates the diabetes-induced decreases in antioxidant defense mechanisms. Coenzyme Q9 improves left ventricular performance and reduces myocardial infarct size and cardiomyocyte apoptosis[1][2]. Uses: Scientific research. Group: Natural products. Alternative Names: Ubiquinone Q9; CoQ9; Ubiquinone 9. CAS No. 303-97-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101415. | |
| 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 |
| 10-(4,5-Dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dienyl)decyl Methanesulfonate | 10-(4,5-Dimethoxy-2-methyl-3,6-dioxocyclohexa-1,4-dienyl)decyl Methanesulfonate is an intermediate in the synthesis of Mitoquinol (M372210), an antioxidant mitochondrial-targeted coenzyme Q analog with neuroprotective effects. Group: Biochemicals. Grades: Highly Purified. CAS No. 845959-53-7. Pack Sizes: 50mg, 100mg. Molecular Formula: C20H32O7S. US Biological Life Sciences. | Worldwide |
| 2,3-Dimethoxy-5-methyl-1,4-benzoquinone | 2,3-Dimethoxy-5-methyl-1,4-benzoquinone. Group: Charge transfer complexesmolecular conductors. Alternative Names: Coenzyme Qo. CAS No. 605-94-7. Product ID: 2,3-dimethoxy-5-methylcyclohexa-2,5-diene-1,4-dione. Molecular formula: 182.18. Mole weight: C9H10O4. CC1=CC(=O)C(=C(C1=O)OC)OC. InChI=1S/C9H10O4/c1-5-4-6 (10)8 (12-2)9 (13-3)7 (5)11/h4H, 1-3H3. UIXPTCZPFCVOQF-UHFFFAOYSA-N. >97.0%(T). |  |
| 2,3-Dimethoxy-5-methyl-1,4-hydroquinone | A substituted p-hydroquinone derivative with antioxidant properties and inhibitory effects in lipid peroxidation. It is a free radical scavenger that can potentially be modified to suppress hydrogen peroxide-induced cytotoxicity and DNA damage in relation to affinity for cell membrane. Group: Biochemicals. Alternative Names: 2,3-Dimethoxy-5-methyl-1,4-benzenediol; 2,3-Dimethoxy-5-methylhydroquinone; 2,3-Dimethoxy-5-methyl-1,4-benzohydroquinone; 2, 3-Dimethoxy-5- methyl benzohydroquinone; dihydrocoenzyme Q0; Reduced Coenzyme Q0; Ubiquinol 0. Grades: Highly Purified. CAS No. 3066-90-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 2, 3-Dimethoxy-5-methyl-6-[10-[ (methylsulfonyl) oxy]decyl]-1, 4-benzenediol | 2, 3-Dimethoxy-5-methyl-6-[10-[ (methylsulfonyl) oxy]decyl]-1, 4-benzenediol is an intermediate in the synthesis of Mitoquinol (M372210), an antioxidant mitochondrial-targeted coenzyme Q analog with neuroprotective effects. Group: Biochemicals. Grades: Highly Purified. CAS No. 845959-54-8. Pack Sizes: 50mg, 100mg. Molecular Formula: C20H34O7S. US Biological Life Sciences. | Worldwide |
| 2,3-Dimethoxy-5-methyl-p-benzoquinone | 2,3-Dimethoxy-5-methyl-p-benzoquinone is used in the synthesis of a variety of polyprenylated quinones. Applications: Used in the synthesis of a variety of polyprenylated quinones. Group: Coenzymes. Synonyms: Coenzyme Q0. CAS No. 605-94-7. Purity: ≥98%. Mole weight: 182.17. Appearance: Crystalline powder. Form: Solid. Coenzyme Q0; 2,3-Dimethoxy-5-methyl-p-benzoquinone; 605-94-7. Cat No: COEC-052. | |
| (2E,6E,10E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol | Used in the preparation of coenzymes Q, vitamin K and polyprenylquinones. Group: Biochemicals. Alternative Names: (E,E,E)-2,6,10-Trimethyl-12-(phenylmethoxy)-2,6,10-dodecatrien-1-ol. Grades: Highly Purified. CAS No. 71135-48-3. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 2-Nicotinamide-2,3,5-tri-O-acetyl-b-D-riboside bromide | 2-Nicotinamide-2,3,5-tri-O-acetyl-b-D-riboside bromide, a highly intriguing and multifaceted biomedicine, unveils its remarkable therapeutic prowess in combating an array of afflictions. Serving as an invaluable forerunner to nicotinamide adenine dinucleotide (NAD+), a quintessential coenzyme orchestrating cellular energy metabolism, this exceptional compound exhibits vast potential in lending respite to maladies encompassing cancer, neurodegenerative disorders, and metabolic aberrations. Gifting unparalleled regulation of cellular processes and DNA reparation, its impact on the intricate machinery of life is undoubtedly profound. Synonyms: 3-carbamoyl-1-(tri-O-acetyl-α-D-ribofuranosyl)-pyridinium,bromide; NICOTINAMIDE-BETA-D-RIBOSIDE-2,3,5-TRIACETATE BROMIDE. CAS No. 78687-38-4. Molecular formula: C17H21BrN2O8. Mole weight: 461.26. | |
| 4-(2-Quinoxalinyl-3-butene-1,2-diol | 4-(2-Quinoxalinyl-3-butene-1,2-diol. Applications: An oxomolybdoenzyme cofactor. Group: Coenzymes. CAS No. 127196-36-5. Mole weight: 216.24. 4-(2-Quinoxalinyl-3-butene-1,2-diol; 127196-36-5. Cat No: COEC-075. | |
| 5-Methyl-dCDP | 5-Methyl-dCDP , an integral intermediary in the bioresearch and development of coenzyme Q10, embodies paramount significance towards cellular well-being by acting as a pivotal antioxidant within every cell membrane. Its profound potential manifests in the research of diverse oxidative stress-driven ailments, including neurodegenerative afflictions and cardiovascular maladies. Synonyms: 5-Methyl-2'-deoxycytidine-5'-diphosphate, Sodium salt. Grade: ≥ 95% by HPLC. Molecular formula: C10H17N3O10P2 (free acid). Mole weight: 401.20 (free acid). | |
| 5-Phospho-D-ribose 1-diphosphate pentasodium salt | 5-Phospho-D-ribose 1-diphosphate pentasodium salt, a quintessential biochemical of paramount importance, is employed for examining the intricacies of nucleotide metabolism and bioenergetics. It unreservedly acts as an integral instrument in synthesizing NAD, an imperative coenzyme that subsumes metabolic reactions and DNA repair. Additionally, it is a tool that can be utilized for unraveling the mysteries of how purine nucleotides corral erythrocyte metabolism, and showcasing the effects of oxidative stress on cellular metabolism. Synonyms: α-D-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), sodium salt (1:5); PRPP pentasodium salt; α-D-Ribofuranose, 5-(dihydrogen phosphate) 1-(trihydrogen diphosphate), pentasodium salt; 5-Phospho-α-D-ribose-1-diphosphate pentasodium salt; 5-Phosphorylribose 1-α-diphosphate pentasodium salt; PP-Ribose-P pentasodium salt. CAS No. 108321-05-7. Molecular formula: C5H8Na5O14P3. Mole weight: 499.98. | |
| 7,8-Dihydro-L-biopterin | 7,8-dihydro-L-Biopterin is a precursor of BH4 synthesis and a noncompetitive inhibitor of GCH-I (GTP cyclohydrolase I), with a Ki of 14.4 μM. Applications: A precursor of bh4 synthesis. Group: Coenzymes. Synonyms: BH2; Dihydrobiopterin; Quinonoid dihydrobiopterin. CAS No. 6779-87-9. Purity: ≥98%. Mole weight: 239.23. Appearance: Powder. Form: Solid. BH2; Dihydrobiopterin; Quinonoid dihydrobiopterin; 7,8-Dihydro-L-biopterin; 6779-87-9. Cat No: COEC-066. | |
| AMPK Signaling Agonist, F17 (4-hydroxy-1-isobutyl-N-(5-methylthiazol-2-yl)-2-oxo-1,2-dihydroquinoline-3-carboxamide) | A cell-permeable 4-hydroxy-2-oxo quinoline carboxamide that acts as an agonist of AMPK signaling. It is shown to reduce fat storage in C. elegans (EC50 ~0.1uM) and reduce the expression level of fat-7 (a C. elegans ortholog of mammalian stearoyl-CoA desaturase-1), through aak-1 (an ortholog for the AMPK-a1 catalytic subunit) and K08F8.2 (a transcription factor) dependent mechanisms. In addition, it markedly reduces the number of lipid droplets in HepG2 human hepatocarcinoma cells at 25uM, and elicits the phosphorylation and inactivation of acetyl coenzyme A carboxylase (ACC, the enzyme that catalyzes the rate-limiting step in de novo fatty acid synthesis). F17-induced ACC phosphorylation can be abrogated by simultaneous treatment with an AMPK inhibitor compound C. Group: Biochemicals. Grades: Highly Purified. CAS No. 280112-24-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Calcium L-ascorbate dihydrate | Calcium L-ascorbate dihydrate. Synonyms: L-Ascorbic acid calcium salt dihydrate, Vitamin C calcium salt. CAS No. 5743-28-2. Pack Sizes: 100 g. Product ID: CDC10-0038. Molecular formula: C12H14CaO12 2H2O. Category: Antioxidant Cosmetic Chemicals. Product Keywords: Cosmetic Ingredients; Antioxidant Cosmetic Chemicals; Calcium L-ascorbate dihydrate; CDC10-0038; 5743-28-2; C12H14CaO12 2H2O; L-Ascorbic acid calcium salt dihydrate,; Vitamin C calcium salt; 227-261-5; MFCD00149216; 5743-28-2. Purity: 0.99. Color: White to slightly yellow. EC Number: 227-261-5. Physical State: Powder. Solubility: Freely soluble in water, practically insoluble in ethanol (96 per cent). Quality Level: 100. Storage: Inert atmosphere,Room Temperature. Application: Calcium L-ascorbate dihydrate is a physiological antioxidant and coenzyme. Boiling Point: N/A. Melting Point: 166 °C (dec.) (lit.). | |
| CoQ-10 | CoQ-10. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Coenzyme Q10. Product Category: Promotional Products. Appearance: solid. CAS No. 303-98-0. Molecular formula: C59H90O4. Mole weight: 863.34. Purity: 95+%. Product ID: ACM303980-4. Alfa Chemistry ISO 9001:2015 Certified. Categories: CoQ 10. | |
| D-Amino acid dehydrogenase, Recombinant | D-amino-acid dehydrogenase (EC 1.4.99.1) is a bacterial enzyme that catalyses the oxidation of D-amino acids into their corresponding oxoacids. It contains both flavin and nonheme iron as cofactors. The enzyme has a very broad specificity and can act on most D-amino acids. D-amino acid + H2O + acceptor <=> a 2-oxo acid + NH3 + reduced acceptor. This reaction is distinct from the oxidation reaction catalysed by D-amino acid oxidase that uses oxygen as a second substrate, as the dehydrogenase can use many different compounds as electron acceptors, with the physiological substrate being coenzyme Q. D-amino-acid dehydrogenase is used in enzyme assays to measure substrate specificity of D-amino acids, such as DauA. Applications: D-amino-acid dehydrogenase is a bacterial enzyme that catalyses the oxidation of d-amino acids into their corresponding oxoacids. it contains flavin and nonheme iron as cofactors and has a broad specificity thereby acting on most d-amino acids. Group: Enzymes. Synonyms: D-Amino acid dehydrogenase; EC 1.4.99.1; 37205-44-0. Enzyme Commission Number: EC 1.4.99.1. CAS No. 37205-44-0. D-Amino acid dehydrogenase. Activity: >26 U/g. Storage: Store at 2-8°C. Source: E. coli. D-Amino acid dehydrogenase; EC 1.4.99.1; 37205-44-0. Cat No: NATE-0825. | |
| Decanoyl coenzyme A monohydrate | Decanoyl coenzyme A is coupled with S-adenosylmethionine (SAM) by Vibrio cholera CqsA enzyme to produce a potent quorum-sensing molecule, 3-aminotridec-2-en-4-one (Ea-CAI-1). Applications: A fatty acyl coa. Group: Coenzymes. Synonyms: Decanoyl CoA Monohydrate. CAS No. 1264-57-9. Purity: ≥90%. Mole weight: 939.8. Appearance: Powder. Form: Solid. Decanoyl CoA Monohydrate; Decanoyl coenzyme A monohydrate; 1264-57-9. Cat No: COEC-051. | |
| Decylubiquinone | Decylubiquinone is an analog of ubiquinone (coenzyme Q 10 ). Decylubiquinone blocks reactive oxygen species (ROS) production in response to glutathione depletion and inhibits activation of the mitochondrial permeability transition [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 55486-00-5. Pack Sizes: 5 mg (77.53 mM * 200 μL in Ethanol); 10 mg (77.53 mM * 400 μL in Ethanol). Product ID: HY-121134. | |
| (E)-Pterulinic acid | (E)-Pterulinic acid is a Coenzyme I: Coenzyme Q oxidoreductase inhibitor produced by Pterula sp. 82168. It has anti-yeast and filamentous fungus effect and has cytotoxic activity. Synonyms: ME-82168-N; Pterulinic acid. CAS No. 190143-30-7. Molecular formula: C15H11ClO4. Mole weight: 290.70. | |
| fumarate reductase (CoM/CoB) | The enzyme, isolated from the archaeon Methanobacterium thermoautotrophicum, is very oxygen sensitive. It cannot use reduced flavins, reduced coenzyme F420, or NAD(P)H as an electron donor. Distinct from EC 1.3.1.6 [fumarate reductase (NADH)], EC 1.3.5.1 [succinate dehydrogenase (ubiquinone)], and EC 1.3.5.4 [fumarate reductase (quinol)]. Group: Enzymes. Synonyms: thiol:fumarate reductase; Tfr. Enzyme Commission Number: EC 1.3.4.1. 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-1384; fumarate reductase (CoM/CoB); EC 1.3.4.1; thiol:fumarate reductase; Tfr. Cat No: EXWM-1384. | |
| Hymeglusin | It is a β-lactone antibiotic produced by the strain of Cephalosporium sp. It has a strong inhibitory effect on hydroxymethyl glutaryl coenzyme A (HMG-CoA) synthase. Synonyms: Hymeglusin; Antibiotic 1233A; 29066-42-0; L-659,699; (2E,4E,7R)-11-[(2R,3R)-3-(hydroxymethyl)-4-oxooxetan-2-yl]-3,5,7-trimethylundeca-2,4-dienoic acid; 2,4-Undecadienoic acid, 11-[(2R,3R)-3-(hydroxymethyl)-4-oxo-2-oxetanyl]-3,5,7-trimethyl-, (2E,4E,7R)-; Antibiotic F 244; (R,R)-Hymeglusin; L 659699; F 244; F-244; SCHEMBL613745; CHEMBL470269; GTPL5886; CHEBI:191049; DTXSID901318499; (R,2E,4E)-11-((2R,3R)-3-(hydroxymethyl)-4-oxooxetan-2-yl)-3,5,7-trimethylundeca-2,4-dienoic acid; HB3701; AKOS032946337; 2,4-Undecadienoic acid, 11-(3-(hydroxymethyl)-4-oxo-2-oxetanyl)-3,5,7-trimethyl-, (2R-(2-alpha(2E,4E,7R*),3-beta))-; HY-117430; CS-0065979; G13092; J-017379; Q27078398; 11-[3R-(hydroxymethyl)-4-oxo-2R-oxetanyl]-3,5,7R-trimethyl-2E,4E-undecadienoic acid. Grade: ≥95%. CAS No. 29066-42-0. Molecular formula: C29H28ClFN6O3. Mole weight: 563. | |
| Idebenone | Idebenone, a well-appreciated mitochondrial protectant, exhibits protective efficacy against neurotoxicity and can be used for the research of Alzheimer's disease, Huntington's disease. Idebenone (oxidised form) has a dose-dependent inhibitory effect on the enzymatic metabolism of arachidonic acid in astroglial homogenates (IC 50 =16.65 μM) [1]. Idebenone, a coenzyme Q10 analog and an antioxidant, induces apoptotic cell death in the human dopaminergic neuroblastoma SHSY-5Y cells [2]. Idebenone quickly crosses the blood-brain barrier. Uses: Scientific research. Group: Signaling pathways. CAS No. 58186-27-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-N0303. | |
| Idebenone | Idebenone is a synthetic analog of coenzyme Q10 (CoQ10) and a brain stimulant. Idebenone is a smart promoting drug, which is mainly used in the treatment of many degenerative diseases of the central nervous system related to oxidative compressions, such as Parkinson's disease, Alzheimer's disease, multi-infarct dementia, cerebral anemia and cerebral failure, and is also used in the treatment of Friedreich's ataxia. It can also be used in cosmetic formulations to clear free radicals, inhibit lipid peroxidation, inhibit inflammation, inhibit DNA damage, photoprotection, reduce pigmentation, and other cosmetic effects. Synonyms: CV 2619; CV-2619; CV2619; Catena; Raxone; Sovrima; 2-(10-Hydroxydecyl)-5,6-dimethoxy-3-methyl-2,5-cyclohexadiene-1,4-dione; 2,3-Dimethoxy-5-methyl-6-(10-hydroxydecyl)-1,4-benzoquinone; 2,3-Dimethoxy-6-(10-hydroxydecyl)-5-methyl-1,4-benzoquinone; 2-(10-Hydroxy-decyl)-5,6-dimethoxy-3-methyl-[1,4]benzoquinone; Avan; Daruma; Hydroxydecyl ubiquinone; Mnesis. Grade: >98%. CAS No. 58186-27-9. Molecular formula: C19H30O5. Mole weight: 338.44. | |
| Idebenone-d6 | Idebenone-d6 is a labelled Idebenone. Idebenone is a synthetic analogue of coenzyme Q10. It is indicated for the treatment of Alzheimer's disease. Synonyms: 2-(10-hydroxydecyl)-5,6-dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione-d6. Grade: > 95%. Molecular formula: C19H24O5D6. Mole weight: 344.48. | |
| methanol O-anthraniloyltransferase | The enzyme from Concord grape (Vitis labrusca) is solely responsible for the production of O-methyl anthranilate, an important aroma and flavor compound in the grape. The enzyme has a broad substrate specificity, and can use a range of alcohols with substantial activity, the best being butanol, benzyl alcohol, iso-pentanol, octanol and 2-propanol. It can use benzoyl-CoA and acetyl-CoA as acyl donors with lower efficiency. In addition to O-methyl anthranilate, the enzyme might be responsible for the production of ethyl butanoate, methyl-3-hydroxy butanoate and ethyl-3-hydroxy butanoate, which are present in large quantities in the grapes. Also catalyses EC 2.3.1.196, benzyl alcohol O-benzoyltransferase. Group: Enzymes. Synonyms: AMAT; anthraniloyl-coenzyme A (CoA):methanol acyltransferase. Enzyme Commission Number: EC 2.3.1.232. 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-2180; methanol O-anthraniloyltransferase; EC 2.3.1.232; AMAT; anthraniloyl-coenzyme A (CoA):methanol acyltransferase. Cat No: EXWM-2180. | |
| Methoxatin disodium salt | Methoxatin disodium salt. Applications: An organic enzyme cofactor. Group: Coenzymes. Synonyms: Pyrrolo-quinoline-quinone disodium salt; PQQ. CAS No. 122628-50-6. Purity: ≥97%. Mole weight: 374.17. Pyrrolo-quinoline-quinone disodium salt; PQQ; Methoxatin disodium salt; 122628-50-6. Cat No: COEC-078. | |
| Mitoquinol | Mitoquinol is a mitochondrial-targeted coenzyme Q analog. Mitoquinol is an antioxidant that inhibits lipid peroxidation. Mitoquinol can be used in vascular disease research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 845959-55-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-124410. | |
| NADH:ubiquinone reductase (H+-translocating) | A flavoprotein (FMN) containing iron-sulfur clusters. The complex is present in mitochondria and aerobic bacteria. Breakdown of the complex can release EC 1.6.99.3, NADH dehydrogenase. In photosynthetic bacteria, reversed electron transport through this enzyme can reduce NAD+ to NADH. Group: Enzymes. Synonyms: ubiquinone reductase (ambiguous); type 1 dehydrogenase; complex 1 dehydrogenase; coenzyme Q reductase (ambiguous); complex I (electron transport chain); complex I (mitochondrial electron transport); complex I (NADH:Q1 oxidoreductase); dihydronicotinamide adenine dinucleotide-coenzyme Q reductase (ambiguous); DPNH-coenzyme Q reductase (. Enzyme Commission Number: EC 7.1.1.2 (Formerly EC 1.6.5.3). CAS No. 9028-04-0. 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-1592; NADH:ubiquinone reductase (H+-translocating); EC 1.6.5.3; 9028-04-0; ubiquinone reductase (ambiguous); type 1 dehydrogenase; complex 1 dehydrogenase; coenzyme Q reductase (ambiguous); complex I (electron transport chain); complex I (mitochondrial electron transport); complex I (NADH:Q1 oxidoreductase); dihydronicotinamide adenine dinucleotide-coenzyme Q reductase (ambiguous); DPNH-coenzyme Q reductase (ambiguous); DPNH-ubiquinone reductase (ambiguous); mitochondrial electron transp | |
| NADH:ubiquinone reductase (non-electrogenic) | A flavoprotein (FAD). Occurs in mitochondria of yeast and plants, and in aerobic bacteria. Has low activity with NADPH. Group: Enzymes. Synonyms: ubiquinone reductase (ambiguous); coenzyme Q reductase (ambiguous); dihydronicotinamide adenine dinucleotide-coenzyme Q reductase (ambiguous); DPNH-coenzyme Q reductase (ambiguous); DPNH-ubiquinone reductase (ambiguous); NADH-coenzyme Q oxidoreductase (ambiguous); NADH-coenzyme Q reductase (ambiguous); NADH-C. Enzyme Commission Number: EC 1.6.5.9. CAS No. 9028-04-0. 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-1598; NADH:ubiquinone reductase (non-electrogenic); EC 1.6.5.9; 9028-04-0; ubiquinone reductase (ambiguous); coenzyme Q reductase (ambiguous); dihydronicotinamide adenine dinucleotide-coenzyme Q reductase (ambiguous); DPNH-coenzyme Q reductase (ambiguous); DPNH-ubiquinone reductase (ambiguous); NADH-coenzyme Q oxidoreductase (ambiguous); NADH-coenzyme Q reductase (ambiguous); NADH-CoQ oxidoreductase (ambiguous); NADH-CoQ reductase (ambiguous); NADH-ubiquinone reductase (ambiguous); NADH-ubiquinone oxidoreductase (ambiguous); reduced nicotinamide adenine dinucleotide-coenzyme Q reductase (ambiguous); NADH-Q6 oxidoreductase (ambiguous); NADH2 dehydrogenase (ubiquinone) (ambiguous). Cat No: EXWM-1598. | |
| Orsellinic acid | Orsellinic acid is from Chaetomium globosum endophytic. Orsellinic acid can block platelet activating factor (PAF)-mediated neuronal apoptosis without affecting G-protein coupled receptor (PAFR)-mediated neuroprotection, and it can effectively attenuate PAFR-independent neuronal apoptosis. It is a novel benzoquinone ring precursor for antroquinonol and 4-acetylantroquinonol B. It is formed from acetyl-coenzyme Q (CoQ) and malonyl-CoA via polyketide pathway. Synonyms: o-Orsellinic acid; 4,6-Dihydroxy-o-toluic acid. Grade: 99.0%. CAS No. 480-64-8. Molecular formula: C8H8O4. Mole weight: 168.15. | |
| o-succinylbenzoate-CoA ligase | O-succinylbenzoate CoA ligase (EC 6.2.1.26), encoded from the menE gene in Escherichia coli, catalyzes the fifth reaction in the synthesis of menaquinone (vitamin K2). This pathway is called 1, 4-dihydroxy-2-naphthoate biosynthesis I. Vitamin K is a quinone that serves as an electron transporter during anaerobic respiration. This process of anaerobic respiration allows the bacteria to generate the energy required to survive. Group: Enzymes. Synonyms: o-succinylbenzoyl-coenzyme A synthetase; o-succinylbenzoate:CoA ligase (AMP-forming). Enzyme Commission Number: EC 6.2.1.26. CAS No. 72506-70-8. 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-5684; o-succinylbenzoate-CoA ligase; EC 6.2.1.26; 72506-70-8; o-succinylbenzoyl-coenzyme A synthetase; o-succinylbenzoate:CoA ligase (AMP-forming). Cat No: EXWM-5684. | |
| 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 |
| Pentapeptide-34 Trifluoroacetate | Pentapeptide-34 Trifluoroacetate, also known as Peptide Q10, is an anti-aging peptide that is inspired by the antioxidant properties of coenzyme Q10. It works by enhancing the natural endogenous synthesis of CoQ10, which is a substance that decreases with age and is crucial for energy production and as a powerful antioxidant in the body. This peptide helps protect the skin against free radicals, which can contribute to premature aging. It is used in various anti-aging personal care products and is known to significantly reduce the appearance of wrinkles, particularly around the eyes and forehead. In summary, Pentapeptide-34 Trifluoroacetate is a valuable ingredient in skincare for its ability to combat the signs of aging and protect the skin from oxidative stress. Synonyms: Peptide Q10; Ala-Val-Leu-Ala-Gly TFA. Grade: ≥95%. | |
| Pterulone | Pterulone is a Coenzyme I: Coenzyme Q oxidoreductase inhibitor produced by Pterula sp. 82168. It has anti-yeast and filamentous fungus effect. Synonyms: (E)-Pterulone; Pterulone A. Grade: 95%. CAS No. 190143-31-8. Molecular formula: C13H11ClO2. Mole weight: 234.68. | |
| Pyrroloquinoline quinone | Pyrroloquinoline quinone is a cofactor of microbial quinoprotein enzyme, and imidazopyrroline. A redox/cofactor found in a a class of enzymes called quinoproteins. Applications: A redox/cofactor found in a a class of enzymes called quinoproteins. Group: Coenzymes. Synonyms: PQQ. CAS No. 72909-34-3. Mole weight: 330.2. Form: Solid. PQQ; Pyrroloquinoline quinone; 72909-34-3. Cat No: COEC-076. | |
| quinate O-hydroxycinnamoyltransferase | Caffeoyl-CoA and 4-coumaroyl-CoA can also act as donors, but more slowly. Involved in the biosynthesis of chlorogenic acid in sweet potato and, with EC 2.3.1.98 chlorogenate-glucarate O-hydroxycinnamoyltransferase, in the formation of caffeoyl-CoA in tomato. Group: Enzymes. Synonyms: hydroxycinnamoyl coenzyme A-quinate transferase. Enzyme Commission Number: EC 2.3.1.99. CAS No. 60321-02-0. 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-2281; quinate O-hydroxycinnamoyltransferase; EC 2.3.1.99; 60321-02-0; hydroxycinnamoyl coenzyme A-quinate transferase. Cat No: EXWM-2281. | |
| quinol-cytochrome-c reductase | The enzyme, often referred to as the cytochrome bc1 complex or complex III, is the third complex in the electron transport chain. It is present in the mitochondria of all aerobic eukaryotes and in the inner membranes of most bacteria. The mammalian enzyme contains cytochromes b-562, b-566 and c1, and a 2-iron ferredoxin. Depending on the organism and physiological conditions, the enzyme extrudes either two or four protons from the cytoplasmic to the non-cytoplasmic compartment (cf. EC 1.6.99.3, NADH dehydrogenase). Group: Enzymes. Synonyms: ubiquinol-cytochrome-c reductase; coenzyme Q-cytochrome c reductase; dihydrocoenzyme Q-cytochrome c reductase; reduced ubiquinone-cytochrome c reductase; complex III (mitocho. Enzyme Commission Number: EC 1.10.2.2. CAS No. 9027-3-6. 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-0474; quinol-cytochrome-c reductase; EC 1.10.2.2; 9027-03-6; ubiquinol-cytochrome-c reductase; coenzyme Q-cytochrome c reductase; dihydrocoenzyme Q-cytochrome c reductase; reduced ubiquinone-cytochrome c reductase; complex III (mitochondrial electron transport); ubiquinone-cytochrome c reductase; ubiquinol-cytochrome c oxidoreductase; reduced coenzyme Q-cytochrome c reductase; ubiquinone-cytochrome c oxidoreductase; reduced ubiquinone-cytochrome c oxido | |
| Tetrahydrobiopterin (THB) dihydrochloride | Tetrahydrobiopterin (THB) dihydrochloride is an activating Nitric Oxide Synthase (NOS)cofactor used in a variety of applications. The compound is also a known cofactor for the monooxygenases that hydroxylates phenylalanine, tyrosine, and tryptophan. Synthesis of THB has been documented to be the rate limiting step in the metabolism of phenylalanine and the biosynthesis of neurotransmiter amines. In mice, Quinolinic acid (sc-203226) induced convulsions were potentiated with Tetrahydrobiopterin dihydrochloride demonstrating that endogenous NO may be involved in stimulating the NMDA receptors. When hypertensive mice were fed THB, but were not introduced to hydralazine or tetrahydroneopterin, they displayed improved cardiac THB stores, phosphorylated phospholamban levels, and diastolic dysfunction. The compound has also been observed as an essential cofactor in the hydroxylation process in mammalian brains. Applications: An activating nos cofactor. Group: Coenzymes. Synonyms: (6R)-5,6,7,8-Tetrahydro-L-biopterin dihydrochloride. CAS No. 69056-38-8. Purity: ≥98%. Mole weight: 314.17. Appearance: Powder. Form: Solid. (6R)-5,6,7,8-Tetrahydro-L-biopterin dihydrochloride; Tetrahydrobiopterin (THB) dihydrochloride; 69056-38-8. Cat No: COEC-024. | |
| Ubidecarenone | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Ubiquinone 10, Li-Q-Sorb, Ubiquinone 50, Unispheres Q 10, (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, Kudesan, p-Benzoquinone, 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- (8CI), PureSorb Q 40, Q 10AA, Vitamin Q, Ensorb, Kaneka Q10, Q-Gel 100,Ubidecarenone, Q-absorb, NSC 140865, Q-Gel, 2,5-Cyclohexadiene-1,4-dione, 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-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- (9CI), Ubiquinone Q10, Liquid-Q, Neuquinon, Aqua Q 10L10, Bio-Quinone Q10, Adelir, 2,5-Cyclohexadiene-1,4-dione, 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-, (all-E)-, Aqua Q10, Coenzyme Q10 (6CI), Ubiquinone, Q10, 2-[(all-E)-3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylbenzene-1,4-dione, CoQ10, Aqua-Q 10P40, Neuquinone, Cosmesome Q 10, Bio-Quinon, Cudesan. | |
| Ubidecarenone for system suitability | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Kaneka Q10, Aqua Q 10L10, Ubiquinone Q10, Unispheres Q 10, (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, Kudesan, Aqua Q10, PureSorb Q 40, Bio-Quinon, Cosmesome Q 10,Ubidecarenone, Li-Q-Sorb, Q-absorb, NSC 140865, CoQ10, Ubiquinone 50, Adelir, Ensorb, Q-Gel, Q-Gel 100, Neuquinone, Ubiquinone 10, 2,5-Cyclohexadiene-1,4-dione, 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-, (all-E)-, 2,5-Cyclohexadiene-1,4-dione, 2-[(2E,6E,10E,14E,18E,22E,26E,30E,34E)-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- (9CI), Q10, Ubiquinone, Liquid-Q, Coenzyme Q10 (6CI), Q 10AA, Vitamin Q, Neuquinon, Bio-Quinone Q10, Cudesan, p-Benzoquinone, 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- (8CI), 2-[(all-E)-3,7,11,15,19,23,27,31,35,39-Decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaenyl]-5,6-dimethoxy-3-methylbenzene-1,4-dione, Aqua-Q 10P40. | |
| Ubiquinol | Reduced coenzyme Q for improving nervous system cell functions. Group: Biochemicals. Alternative Names: 2-[(2E, 6E, 10E, 14E, 18E, 22E, 26E, 30E, 34E)-3, 7, 11, 15, 19, 23, 27, 31, 35, 39-Decamethyl-2, 6, 10, 14, 18, 22, 26, 30, 34, 38-tetracontadecaen-1-yl]-5, 6-dimethoxy-3-methyl- 1,4-benzenediol; Dihydrocoenzyme Q10; Reduced Coenzyme Q10; Reduced Ubiquinone Q10; Ubiquinol 50. Grades: Highly Purified. CAS No. 992-78-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Ubiquinone-1 | Ubiquinone-1 is an intermediate in the synthesis of Coenzyme Q. Ubiquinone-1 can be reduced by NADPH oxidase, hepatoma cells, Ascorbic acid (HY-B0166)[1][2][3][4][5]. Uses: Scientific research. Group: Natural products. CAS No. 727-81-1. Pack Sizes: 1 mg (40 mM * 100 ?L in Ethanol); 5 mg (40 mM * 500 ?L in Ethanol); 10 mg (40 mM * 1 mL in Ethanol); 25 mg (40 mM * 2.5 mL in Ethanol); 50 mg (40 mM * 5 mL in Ethanol); 100 mg (40 mM * 10 mL in Ethanol). Product ID: HY-113449. | |
| Ubiquinone-10 | Ubiquinone-10 acts as an inhibitor of the mitochondrial permeability transition pore (MPTP). This inhibitory effect can be counteracted by ubiquinone-5. Applications: An inhibitor of the mitochondrial permeability transition pore. Group: Coenzymes. Synonyms: Coenzyme Q2; 2,3-Dimethoxy-5-methyl-6-geranyl-1,4-benzoquinone. CAS No. 606-06-4. Purity: ≥90%. Mole weight: 318.4. Form: Liquid. Coenzyme Q2; 2,3-Dimethoxy-5-methyl-6-geranyl-1,4-benzoquinone; Ubiquinone-10; 606-06-4. Cat No: COEC-062. | |
| Ubiquinone-5 | Ubiquinone-5 is a coenzyme Q10 (CoQ10) (sc-205262) analog that counteracts the inhibitory effects on mitochondrial permeability transition pore (MPTP) of decylubiquinone and ubiquinone-10. Applications: A coq10 analog that counteracts the inhibitory effects on mptp. Group: Coenzymes. Synonyms: Coenzyme Q1. CAS No. 727-81-1. Mole weight: 250.29. Form: Liquid. Coenzyme Q1; Ubiquinone-5; 727-81-1. Cat No: COEC-012. | |
| (Z)-Pterulinic Acid | (Z)-Pterulinic Acid is a Coenzyme I: Coenzyme Q oxidoreductase inhibitor produced by Pterula sp. 82168. It has anti-yeast and filamentous fungus effect and has cytotoxic activity. CAS No. 530087-05-9. Molecular formula: C15H11ClO4. Mole weight: 290.70. | |
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