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| Product | Description | |
|---|---|---|
| Pyridoxal-5-phosphate | Pyridoxal-5-phosphate functions as a coenzyme in the metabolism of amino acids, carbohydrates, lipids, and proteins. Applications: A coenzyme for amino acid synthesis. Group: Coenzymes. Synonyms: Codecarboxylase. CAS No. 54-47-7. Purity: ≥98%. Mole weight: 247.14. Form: Solid. Codecarboxylase; Pyridoxal-5-phosphate; 54-47-7. Cat No: COEC-006. |  |
| Pyridoxal-5-Phosphate | A derivative of Pyridoxine. Pyridoxine is a form of vitamin B6 found commonly in food and used as dietary supplement. It can be used to treat and prevent pyridoxine deficiency, sideroblastic anaemia, pyridoxine-dependent epilepsy, certain metabolic disorders, problems from isoniazid, and mushroom poisoning. Vitamin supplement in health care products. Uses: Ingredient of health care products. Synonyms: 3-Hydroxy-2-methyl-5-[(phosphonooxy)methyl]-4-pyridinecarboxaldehyde; Pyridoxal Phosphate; Pyridoxal 5-(Dihydrogen Phosphate); 2-Methyl-3-hydroxy-4-formyl-5- pyridyl-methylphosphoric Acid; 3-Hydroxy-5-(hydroxymethyl)-2-methyl- isonicotinaldehyde 5-Phosphate; Apolon B6; Biosechs; Codecarboxylase; Coenzyme B6; Hairoxal; Hexermin P; Hi-Pyridoxin; Hiadelon; NSC 82388; PLP; Phosphopyridoxal; Piodel; Pydoxal; Pyridoxal Monophosphate; Vitazechs. Grades: > 95%. CAS No. 54-47-7. Molecular formula: C8H10NO6P. Mole weight: 247.15. |  |
| Pyridoxal-5-phosphate 98+% | Pyridoxal-5-phosphate 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g, 1Kg. US Biological Life Sciences. |  Worldwide |
| Pyridoxal-5-phosphate hydrate | Pyridoxal-5-phosphate hydrate. Group: Biochemicals. Alternative Names: 3- hydroxy-2- methyl -5- ( [phosphonooxy] methyl ) -4-pyridinecarboxalde hyde; Pyridoxal 5'-(dihydrogen phosphate). Grades: Highly Purified. CAS No. 853645-22-4. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H10NO6P·xH2O. US Biological Life Sciences. | Worldwide |
| α,γ-Homocysteinase from Trichomonas vaginalis, Recombinant | Recombinant Homocysteine α,γ-lyase is a pyridoxal-5-phosphate dependent enzyme. It is a mutant of homocysteinase from Trichomonas vaginalis encoded by mgl1 gene, containing three point mutations, such as; Phe47Leu, Asp172Glu, Ser308Tyr. The enzyme can metabolize homocysteine into α-keto butyrate, hydrogen sulfide and ammonia. Group: Enzymes. Synonyms: α,γ-Homocysteinase; Methionine gamma-lyase; mgl1. Purity: > 95% by SDS-PAGE. α,γ-Homocysteinase. Mole weight: 43 kDa. Activity: > 5 mU/mg. Storage: Reconstituted enzyme can be stored in working aliquots at -20°C and use within 3 months. Avoid repeated freeze-thaw cycles. Form: Lyophilized. Source: E. coli and fused to His-tag at N-terminus. Species: Trichomonas vaginalis. α,γ-Homocysteinase; Methionine gamma-lyase; mgl1; Homocysteine α,γ-Lyase; rHCYase. Cat No: NATE-1640. | |
| Threonine Deaminase (Crude Enzyme) | Threonine ammonia-lyase, also commonly referred to as threonine deaminase or threonine dehydratase, is an enzyme responsible for catalyzing the conversion of L-threonine into alpha-ketobutyrate and ammonia. Alpha-ketobutyrate can be converted into L-isoleucine, so threonine ammonia-lyase functions as a key enzyme in BCAA synthesis. It employs a pyridoxal-5-phosphate cofactor, similar to many enzymes involved in amino acid metabolism. It is found in bacteria, yeast, and plants, though most research to date has focused on forms of the enzyme in bacteria. This enzyme was one of the first in which negative feedback inhibition by the end product of a metabolic pathway was directl...es. Synonyms: threonine deaminase; L-serine dehydratase; serine deaminase; L-threonine dehydratase; threonine dehydrase; L-threonine deaminase; threonine dehydratase; L-threonine hydro-lyase (deaminating); L-threonine ammonia-lyase. Enzyme Commission Number: EC 4.3.1.19. CAS No. 9024-34-4. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. threonine deaminase; L-serine dehydratase; serine deaminase; L-threonine dehydratase; threonine dehydrase; L-threonine deaminase; threonine dehydratase; L-threonine hydro-lyase (deaminating); L-threonine ammonia-lyase. Pack: 100ml. Cat No: NATE-1853. | |
| 2-iminobutanoate/2-iminopropanoate deaminase | This enzyme, which has been found in all species and tissues examined, catalyses the hydrolytic deamination of imine intermediates formed by several types of pyridoxal-5'-phosphate-dependent dehydratases, such as EC 4.3.1.19, threonine ammonia-lyase and EC 4.3.1.17, L-serine ammonia-lyase. The reactions, which can occur spontaneously, are accelerated to minimize the cellular damage that could be caused by these reactive intermediates. Group: Enzymes. Synonyms: yjgF (gene name); ridA (gene name); enamine/imine deaminase (ambiguous). Enzyme Commission Number: EC 3.5.99.10. 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-4586; 2-iminobutanoate/2-iminopropanoate deaminase; EC 3.5.99.10; yjgF (gene name); ridA (gene name); enamine/imine deaminase (ambiguous). Cat No: EXWM-4586. | |
| 7-Azido-4-methylcoumarin (AzMC) | Highly sensitive and selective fluorogenic H2S probe. The aromatic azide moiety of AzMC is selectively reduced in the presence of H2S, producing the fluorescent 7-amino-4- methylcoumarin (AMC) with a concomitant increase in fluorescence with lambdaex=365nm and lambdaem=450nm. Photoaffinity labeling probe for the substrate binding site of human sulfotransferase 1A1 (SULT1A1). Probe to monitor the enzymatic production of H2S in vitro and to visualize H2S in living cells. Tool for monitoring the activity of pyridoxal-5'-phosphate (PLP)-dependent enzymes (e.g. cystathionine beta-synthase (CBS), cystathionine gamma-lyase (CGL) and tryptophan synthase (TS)). Tool to identify novel cystathionine beta-synthase (CBS) inhibitors and activators. Suitable for high-throughput screening. Use of this product with DTT, TCEP and/or biological thiols at concentrations of >25mM should be avoided for maximum efficiency. Group: Biochemicals. Grades: Highly Purified. CAS No. 95633-27-5. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| erythrose-4-phosphate dehydrogenase | This enzyme was originally thought to be a glyceraldehyde-3-phosphate dehydrogenase (EC 1.2.1.12), but this has since been disproved, asglyceraldehyde 3-phosphate is not a substrate. Forms part of the pyridoxal-5'-phosphate coenzyme biosynthesis pathway in Escherichia coli, along with EC 1.1.1.290 (4-phosphoerythronate dehydrogenase), EC 2.6.1.52 (phosphoserine transaminase), EC 1.1.1.262 (4-hydroxythreonine-4-phosphate dehydrogenase), EC 2.6.99.2 (pyridoxine 5'-phosphate synthase) and EC 1.4.3.5 (pyridoxamine-phosphate oxidase). Group: Enzymes. Synonyms: erythrose 4-phosphate dehydrogenase; E4PDH; GapB; Epd dehydrogenase; E4P dehydrogenase. Enzyme Commission Number: EC 1.2.1.72. CAS No. 131554-04-6. 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-1174; erythrose-4-phosphate dehydrogenase; EC 1.2.1.72; 131554-04-6; erythrose 4-phosphate dehydrogenase; E4PDH; GapB; Epd dehydrogenase; E4P dehydrogenase. Cat No: EXWM-1174. | |
| L-Methionine γ-Lyase, Recombinant | L-Methionine γ-Lyase or methioninase has been shown to have anti-tumor effects by depleting methionine from methionine-dependent tumors making them more sensitive to traditional chemotherapies. L-methionine γ-lyase is a pyridoxal phosphate-containing enzyme that converts l-methionine to α-ketobutyrate, ammonia and methyl mercaptan. Applications: L-methionine γ-lyase has been used in a study to assess catabolism of volatile sulfur compound precursors by brevibacterium linens and geotrichum candidum. it has also been used in a study to investigate the enzymatic pr ocessing of fluorinated methionine analogs. Group: Enzymes. Synonyms: L-methioninase; methionine lyase; methioninase; methionine dethiomethylase; L-methionine γ-lyase; L-methionine methanethiol-lyase (deaminating); EC 4.4.1.11; methionine γ-lyase. Enzyme Commission Number: EC 4.4.1.11. CAS No. 42616-25-1. L-Methionine γ-Lyase. Activity: > 0.2 unit/mg solid. Storage: -20°C. Form: Supplied as a lyophilized powder containing pyridoxal-5?-phosphate and potassium phosphate. Source: E. coli. L-methioninase; methionine lyase; methioninase; methionine dethiomethylase; L-methionine γ-lyase; L-methionine methanethiol-lyase (deaminating); EC 4.4.1.11; methionine γ-lyase. Cat No: NATE-0414. | |
| PPNDS | PPNDS is a potent and selective P2X1 receptor antagonist (pKB = 7.43 in rat vas deferens). PNDS is approximately 50-fold less selective for P2Y1R and does not interact with α1A-adrenergic, adenosine A1 and A2B, histamine H1, or muscarinic M3 receptors. Synonyms: Pyridoxal-5'-phosphate-6-(2'-naphthylazo-6'-nitro-4',8'-disulfonate) tetrasodium salt. CAS No. 1021868-77-8. Molecular formula: C18H11N4Na4O14PS2. Mole weight: 694.36. | |
| Pyridoxal-5'- phosphate monohydrate | 5g Pack Size. Group: Analytical Reagents, Biochemicals, Stains & Indicators. Formula: C8H10NO6P ·H2O. CAS No. 41468-25-1. Prepack ID 26067672-5g. Molecular Weight 265.16. See USA prepack pricing. |  |
| Pyridoxal-5'-phosphate monohydrate | Pyridoxal-5'-phosphate monohydrate is a vitamin B6 metabolite that can modify lysyl and valyl residues in proteins. It has the ability to inhibit purinergic receptors and intracellular influx of Ca2+. Pyridoxal-5'-phosphate monohydrate can modify peptides and suppress their precursor ionization efficiency. Research shows that pyridoxal-5'-phosphate-dependent enzymes can be inhibited by cycloserine. Applications: A vitamin b6 metabolite that can modify lysyl and valyl residues in proteins. Group: Coenzymes. Synonyms: Codecarboxylase. CAS No. 41468-25-1. Purity: ≥97%. Mole weight: 265.2. Appearance: Powder. Form: Solid. Codecarboxylase; Pyridoxal-5'-phosphate monohydrate; 41468-25-1. Cat No: COEC-044. | |
| Pyridoxal-5'-Phosphate (P5P) | Pyridoxal-5'-Phosphate (P5P). |  CA, FL & NJ |
| pyridoxal 5'-phosphate synthase | A flavoprotein (FMN). In Escherichia coli, the coenzyme pyridoxal 5'-phosphate is synthesized de novo by a pathway that involves EC 1.2.1.72 (erythrose-4-phosphate dehydrogenase), EC 1.1.1.290 (4-phosphoerythronate dehydrogenase), EC 2.6.1.52 (phosphoserine transaminase), EC 1.1.1.262 (4-hydroxythreonine-4-phosphate dehydrogenase), EC 2.6.99.2 (pyridoxine 5'-phosphate synthase) and EC 1.4.3.5 (with pyridoxine 5'-phosphate as substrate). N4'-Substituted pyridoxamine derivatives are also oxidized in reaction (1) to form pyridoxal 5-phosphateand the corresponding primary amine. Group: Enzymes. Synonyms: pyridoxamine 5'-phosphate oxidase; pyridoxamine phosphate oxidase; pyridoxine (pyridoxamine)phosphate oxidase; pyridoxine (pyridoxamine) 5'-phosphate. Enzyme Commission Number: EC 1.4.3.5. CAS No. 9029-21-4. 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-1482; pyridoxal 5'-phosphate synthase; EC 1.4.3.5; 9029-21-4; pyridoxamine 5'-phosphate oxidase; pyridoxamine phosphate oxidase; pyridoxine (pyridoxamine)phosphate oxidase; pyridoxine (pyridoxamine) 5'-phosphate oxidase; pyridoxaminephosphate oxidase (EC 1.4.3.5: deaminating); PMP oxidase; pyridoxol-5'-phosphate:oxygen oxidoreductase (deaminating) (incorrect); pyridoxamine-phosphate oxidase; PdxH. Cat No: EXWM-1482. | |
| Pyridoxamine-5-phosphate | Cas No. 529-96-4. | |
| (S)-3,5-dihydroxyphenylglycine transaminase | A pyridoxal-5'-phosphate protein. The enzyme from the bacterium Amycolatopsis orientalis catalyses the reaction in the reverse direction as part of the biosynthesis of the (S)-3,5-dihydroxyphenylglycine constituent of the glycopeptide antibiotic chloroeremomycin. Group: Enzymes. Synonyms: HpgT. Enzyme Commission Number: EC 2.6.1.103. 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-2843; (S)-3,5-dihydroxyphenylglycine transaminase; EC 2.6.1.103; HpgT. Cat No: EXWM-2843. | |
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