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| Product | Description | |
|---|---|---|
| 27 kDa antibacterial protein | 27 kDa antibacterial protein is an antimicrobial peptide produced by Cyprinus carpio (common carp). It has antibacterial activity against Gram-positive bacteria and Gram-negative bacteria. Synonyms: Gly-Ile-Gly-Gly-Lys-Pro-Val-Gln-Thr-Ala-Phe-Val-Asp-Asn-Asp-Gly-Ile-Tyr-Asp. Grades: >95%. Molecular formula: C87H132N22O30. Mole weight: 1966.13. |  |
| Antibacterial napin | Antibacterial napin is an antimicrobial peptide produced by Brassica rapa subsp. chinensis (Pak-choi). It has antibacterial activity against Gram-negative bacteria and the Gram-positive bacteria. Synonyms: Pro-Ala-Gln-Pro-Phe-Arg-Phe-Pro-Lys-His-Pro-Gln-Gly-Pro-Gln-Thr-Arg-Pro-Pro-Ile; Napin-like Polypeptide. Grades: ≥96%. Molecular formula: C107H162N32O25. Mole weight: 2296.66. | |
| Antibacterial peptide chensirin-1 | Antibacterial peptide chensirin-1 is an antimicrobial peptide isolated from the skin secretion of the Chinese frog Rana chensinensis. It has antimicrobial activity against gram-negative and gram-positive bacteria. Synonyms: Val-Leu-Pro-Leu-Val-Gly-Asn-Leu-Leu-Asn-Asp-Leu-Leu-Gly-Glu; chensirin-1. Grades: 96%. Molecular formula: C72H123N17O22. Mole weight: 1578.87. | |
| Antibacterial peptide Hex-Mag | Antibacterial peptide Hex-Mag is an antimicrobial peptide produced by Synthetic construct. It has antimicrobial activity against gram-negative and gram-positive bacteria. Synonyms: Arg-Arg-Trp-Gln-Trp-Arg-Gly-Ile-Gly-Lys-Phe-Leu-His-Ser-Ala-Lys-Lys-Phe. Grades: ≥96%. | |
| Antibacterial peptide/melittin homolog | Antibacterial peptide/melittin homolog is an antimicrobial peptide and a synthetic analog of Melittin (H-4310). It has antibacterial activity against gram-negative bacteria. Synonyms: Hecate/Antibacterial peptide/melittin homolog; H-Phe-Ala-Leu-Ala-Leu-Lys-Ala-Leu-Lys-Lys-Ala-Leu-Lys-Lys-Leu-Lys-Lys-Ala-Leu-Lys-Lys-Ala-Leu-OH. Grades: >97%. Molecular formula: C123H226N32O24. Mole weight: 2537.35. | |
| Antibacterial peptide PMAP-23 | Antibacterial peptide PMAP-23 is an antimicrobial peptide produced by Sus scrofa (Pig). It has potent antimicrobial activity against Gram-negative and Gram-positive bacteria without hemolytic activity. Synonyms: Myeloid antibacterial peptide 23; PMAP-23; PMAP23; Arg-Ile-Ile-Asp-Leu-Leu-Trp-Arg-Val-Arg-Arg-Pro-Gln-Lys-Pro-Lys-Phe-Val-Thr-Val-Trp-Val-Arg-OH. Grades: ≥95%. Molecular formula: C140H229N43O28. Mole weight: 2962.63. | |
| Antibacterial peptide PMAP-36 | Antibacterial peptide PMAP-36 is an antimicrobial peptide produced by Sus scrofa (Pig). It has antimicrobial activity against Gram-negative and Gram-positive bacteria. Synonyms: Myeloid antibacterial peptide 36; PMAP-36; PMAP36; Gly-Arg-Phe-Arg-Arg-Leu-Arg-Lys-Lys-Thr-Arg-Lys-Arg-Leu-Lys-Lys-Ile-Gly-Lys-Val-Leu-Lys-Trp-Ile-Pro-Pro-Ile-Val-Gly-Ser-Ile-Pro-Leu-Gly-Cys-Gly. Grades: 97%. Molecular formula: C191H336N62O39S. Mole weight: 4157.22. | |
| Antibacterial peptide PMAP-37 | Antibacterial peptide PMAP-37 is an antimicrobial peptide produced by Sus scrofa (Pig). It has antimicrobial activity against Gram-negative and Gram-positive bacteria. Synonyms: Myeloid antibacterial peptide 37; PMAP-37; PMAP37; Gly-Leu-Leu-Ser-Arg-Leu-Arg-Asp-Phe-Leu-Ser-Asp-Arg-Gly-Arg-Arg-Leu-Gly-Glu-Lys-Ile-Glu-Arg-Ile-Gly-Gln-Lys-Ile-Lys-Asp-Leu-Ser-Glu-Phe-Phe-Gln-Ser. Grades: >85%. Molecular formula: C192H320N60O56. Mole weight: 4365.02. | |
| Aspartate aminotransferase, Genetically engineered bacteria | Aspartate aminotransferase, Genetically engineered bacteria (EC 2.6.1.1) (AST) is a transaminase enzyme, is often used in biochemical studies. Aspartate aminotransferase catalyzes aspartate and alpha-ketoglutarate converts to oxaloacetate and glutamate. Aspartate aminotransferase can be found in cerebrospinal fluid, exudates, and transudates [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 2.6.1.1; GOT; AST. CAS No. 9000-97-9. Pack Sizes: 200 U; 1 KU. Product ID: HY-P3016. |  |
| β-D-Glucuronidase from Bacteria, Recombinant | β-glucuronidase catalyzes the breakdown of complex carbohydrates. In humans it converts conjugated bilirubin into the unconjugated form, making bilirubin suitable for reabsorption. Group: Enzymes. Synonyms: β-glucuronide glucuronohydrolase glucuronidase; exo-β-D-glucuronidase; ketodase; EC 3.2.1.31; 9001-45-0; β-D-glucuronoside glucuronosohydrolase; GUSB. Enzyme Commission Number: EC 3.2.1.31. CAS No. 9001-45-0. GUSB. Mole weight: 68 kD (SDS-PAGE). Activity: > 170 U/mg protein. Storage: Below -20°C. Form: Glycerol Solution. Source: E. coli. Species: Bacteria. β-glucuronide glucuronohydrolase glucuronidase; exo-β-D-glucuronidase; ketodase; EC 3.2.1.31; 9001-45-0; β-D-glucuronoside glucuronosohydrolase; GUSB. Cat No: NATE-1036. |  |
| Catalase from Psychrotolerant Bacteria, recombinant | Catalase is an enzyme that catalyzes the transformation of hydrogen peroxide into water and oxygen. This enzyme functions as a natural antioxidant protecting the cell against oxidative damage. This enzyme finds applications in Research and Clinical Chemistry. It also finds diverse industrial applications in textiles, waste treatment, cosmetics and as a disinfectant agent. Group: Enzymes. Synonyms: EC 1.11.1.6; Catalase; equilase; caperase; optidase; catalase-peroxidase; CAT; H2O2:H2O2 oxidoreductase. Enzyme Commission Number: EC 1.11.1.6. CAS No. 9001-5-2. CAT. Mole weight: ~220 kDa. Activity: > 65000 U/mL (Specific activity: > 7500 U/mg). Storage: At -20°C, it keeps activity for at least 18 months. Form: Liquid. Source: E. coli. Species: Psychrotolerant Bacteria. EC 1.11.1.6; Catalase; equilase; caperase; optidase; catalase-peroxidase; CAT; H2O2:H2O2 oxidoreductase. Cat No: NATE-1699. | |
| Catalase from Psychrotolerant Bacteria, recombinant (Lyophilized Powder) | Catalase is an enzyme that catalyzes the transformation of hydrogen peroxide into water and oxygen. This enzyme functions as a natural antioxidant protecting the cell against oxidative damage. This enzyme finds applications in Research and Clinical Chemistry. It also finds diverse industrial applications in textiles, waste treatment, cosmetics and as a disinfectant agent. Group: Enzymes. Synonyms: EC 1.11.1.6; Catalase; equilase; caperase; optidase; catalase-peroxidase; CAT; H2O2:H2O2 oxidoreductase. Enzyme Commission Number: EC 1.11.1.6. CAS No. 9001-5-2. CAT. Mole weight: ~220 kDa. Activity: > 8000 U/mg protein. Storage: At -20°C, it keeps 100% of its activity for more than two years. Form: Lyophilized Powder. Source: E. coli. Species: Psychrotolerant Bacteria. EC 1.11.1.6; Catalase; equilase; caperase; optidase; catalase-peroxidase; CAT; H2O2:H2O2 oxidoreductase. Cat No: NATE-1700. | |
| CECE_BOMMO Antibacterial peptide enbocin precursor | CECE_BOMMO Antibacterial peptide enbocin precursor was found in Bombyx mori. It has antibacterial activity against Gram-positive and Gram-negative bacteria. | |
| Cellulose Nanofiber from Bacteria | Cellulose Nanofiber from Bacteria. Group: Nanofibers. |  |
| D-Lactate dehydrogenase from Bacteria, Recombinant | In enzymology, a D-lactate dehydrogenase is an enzyme that catalyzes the chemical reaction: (D)-lactate + 2 ferricytochrome c<-> pyruvate + 2 ferrocytochrome c. Thus, the two substrates of this enzyme are (D)-lactate and ferricytochrome c, whereas its two products are pyruvate and ferrocytochrome c. This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-OH group of donor with a cytochrome as acceptor. This enzyme participates in pyruvate metabolism. It employs one cofactor, FAD. Group: Enzymes. Synonyms: EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c 2-oxidoreductase; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Enzyme Commission Number: EC 1.1.1.28. CAS No. 9028-36-8. D-LDH. Mole weight: 44 kD (SDS-PAGE). Activity: > 800 U/mg Protein. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. EC 1.1.1.28; D-Lactic Dehydrogenase; 9028-36-8; (D)-lactate:ferricytochrome-c 2-oxidoreductase; lactic acid dehydrogenase; D-lactate (cytochrome) dehydrogenase; cytochrome-dependent D-(-)-lactate dehydrogenase; D-lactate-cytochrome c reductase; D-(-)-lactic cytochrome c reductase. Cat No: NATE-1042. | |
| Hyaluronic acid sodium salt (from bacteria Streptococcus equi) | 500mg Pack Size. Group: Biochemicals, Carbohydrates, Research Organics & Inorganics. Formula: N/A. CAS No. 9067-32-7. Prepack ID 11130212-500mg. See USA prepack pricing. |  |
| Isocitrate dehydrogenase (NAD+) from Bacteria, Recombinant | Isocitrate dehydrogenase (IDH) is an enzyme that catalyzes the oxidative decarboxylation of Isocitrate, producing alpha-ketoglutarate (α-ketoglutarate) and CO2. This is a two-step process, which involves oxidation of Isocitrate (a secondary alcohol) to oxalosuccinate (a ketone), followed by the decarboxylation of the carboxyl group beta to the ketone, forming alpha-ketoglutarate. In humans, IDH exists in three isoforms:IDH3 catalyzes the third step of the citric acid cycle while converting NAD+ to NADH in the mitochondria. The isoforms IDH1 and IDH2 catalyze the same reaction outside the context of the citric acid cycle and use NADP+ as a cofactor instead o...namide adenine dinucleotide Isocitrate dehydrogenase; EC 1.1.1.41. Enzyme Commission Number: EC 1.1.1.41. CAS No. 9001-58-5. IDH. Mole weight: 40 kD (SDS-PAGE). Activity: > 40 Units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. Beta-ketoglutaric-isocitric carboxylase; IDH; Isocitrate dehydrogenase (NAD); Isocitric acid dehydrogenase; Isocitric dehydrogenase; NAD dependent Isocitrate dehydrogenase; NAD Isocitrate dehydrogenase; NAD isocitric dehydrogenase; NAD-linked Isocitrate dehydrogenase; NAD-specific Isocitrate dehydrogenase; Nicotinamide adenine dinucleotide Isocitrate dehydrogenase; EC 1.1.1.41. Cat No: NATE-1041. | |
| Isocitrate Dehydrogenase (NADP+) from Bacteria, Recombinant | Isocitrate dehydrogenase (IDH) (EC 1.1.1.42) is an enzyme that catalyzes the oxidative decarboxylation of Isocitrate, producing alpha-ketoglutarate (α-ketoglutarate) and CO2. This is a two-step process, which involves oxidation of Isocitrate (a secondary alcohol) to oxalosuccinate (a ketone), followed by the decarboxylation of the carboxyl group beta to the ketone, forming alpha-ketoglutarate. In humans, IDH exists in three isoforms:IDH3 catalyzes the third step of the citric acid cycle while converting NAD+ to NADH in the mitochondria. The isoforms IDH1 and IDH2 catalyze the same reaction outside the context of the citric acid cycle and use NADP+ as a cof...rogenase (NADP+); EC 1.1.1.42; IDH; Isocitrate Dehydrogenase; Dual-cofactor-specific Isocitrate dehydrogenase; IDP; Isocitrate (NADP) dehydrogenase; Isocitrate (nicotinamide adenine dinucleotide phosphate) dehydrogenase; Isocitrate dehydrogenase (NADP); Isocitrate dehydrogenase (NADP-dependent); NADP isocitric dehydrogenase; NADP (+)-ICDH; NADP (+)-IDH; NADP (+)-linked Isocitrate dehydrogenase; NADP-dependent Isocitrate dehydrogenase; NADP-dependent isocitric dehydrogenase; NADP-linked Isocitrate dehydrogenase; NADP-specific Isocitrate dehydrogenase; Oxalosuccinate decarboxylase; Oxalsuccinic decarboxylase; Triphosphopyridine nucleotide-linked Isocitrate dehydrog | |
| Malate dehydrogenase from Bacteria, Recombinant | Malate dehydrogenase is an enzyme in the citric acid cycle that catalyzes the conversion of malate into oxaloacetate (using NAD+) and vice versa (this is a reversible reaction). Malate dehydrogenase is not to be confused with malic enzyme, which catalyzes the conversion of malate to pyruvate producing NADPH. Malate dehydrogenase is also involved in gluconeogenesis, the synthesis of glucose from smaller molecules. Pyruvate in the mitochondria is acted upon by pyruvate carboxylase to form oxaloacetate, a citric acid cycle intermediate. In order to get the oxaloacetate out of the mitochondria, malate dehydrogenase reduces it to malate, and it then traverses the inner mit...EC 1.1.1.37; Malate Dehydrogenase. Enzyme Commission Number: EC 1.1.1.37. CAS No. 9001-64-3. MDH. Mole weight: 40 kD (SDS-PAGE). Activity: > 550 units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. malic dehydrogenase; L-malate dehydrogenase; NAD-L-malate dehydrogenase; malic acid dehydrogenase; NAD-dependent malic dehydrogenase; NAD-malate dehydrogenase; NAD-malic dehydrogenase; malate NAD dehydrogenase; NAD-dependent malate dehydrogenase; NAD-sp; ECific malate dehydrogenase; NAD-linked malate dehydrogenase; MDH; L-malate-NAD+ oxidoreductase; S-malate: NAD+ oxidoreductase; EC 1.1.1.37; Malate Dehydrogenase. Cat No: NATE-1038. | |
| Native Bacteria Achromopeptidase | Lysyl endopeptidase (EC 3.4.21.50, Achromobacter proteinase I, Achromobacter lyticus alkaline proteinase I, protease I, achromopeptidase, lysyl bond specific proteinase) is an enzyme. This enzyme catalyses the following chemical reaction:Preferential cleavage:Lys-, including-Lys-Pro-. This enzyme is isolated from Achromobacter lyticus. Hemolysins are lipids and proteins that cause lysis of red blood cells by destroying their cell membrane. although the lytic activity of some microbe-derived hemolysins on red blood cells may be of great importance for nutrient acquisition, many hemolysins produced by pathogens do not cause significant destruction of red blood cells during infe...and the effect of ciprofloxacin on biofilm formation. Group: Enzymes. Synonyms: Achromobacter proteinase I; Achromobacter lyticus alkaline proteinase I; protease I; achromopeptidase; lysyl bond specific proteinase; EC 3.4.21.50; 123175-82-6; Lysyl endopeptidase. Enzyme Commission Number: EC 3.4.21.50. CAS No. 123175-82-6. Achromopeptidase. Mole weight: ~27 kDa. Activity: > 1,000 units/mg solid; > 20,000 units/mg solid. Storage: 2-8°C. Form: lyophilized powder. Source: Bacteria. Achromobacter proteinase I; Achromobacter lyticus alkaline proteinase I; protease I; achromopeptidase; lysyl bond specific proteinase; EC 3.4.21.50; 123175-82-6; Lysyl endopeptidase. Cat No: NATE-0022. | |
| Native Bacteria Maltose phosphorylase | Maltose phosphorylase (MP) is a dimeric enzyme that catalyzes maltose and inorganic phosphate into β-D-glucose-1-phosphate and glucose. Group: Enzymes. Synonyms: maltose phosphorylase; maltose:phosphate 1-β-D-glucosyltransferase; EC 2.4.1.8; 9030-19-7; MP. Enzyme Commission Number: EC 2.4.1.8. CAS No. 9030-19-7. MP. Activity: > 5 units/mg protein (at 25°C and pH 7.5). Storage: 0 -5°C. Form: Ammonium sulfate suspension. Source: Bacteria. maltose phosphorylase; maltose:phosphate 1-β-D-glucosyltransferase; EC 2.4.1.8; 9030-19-7; MP. Cat No: NATE-1031. | |
| Native Fructose-bisphosphate aldolase from Thermophillic bacteria | Fructose-bisphosphate aldolase (EC 4.1.2.13), often just aldolase, is an enzyme catalyzing a reversible reaction that splits the aldol, fructose 1,6-bisphosphate, into the triose phosphates dihydroxyacetone phosphate (DHAP) and glyceraldehyde 3-phosphate (G3P). Aldolase can also produce DHAP from other (3S,4R)-ketose 1-phosphates such as fructose 1-phosphate and sedoheptulose 1,7-bisphosphate. Gluconeogenesis and the Calvin cycle, which are anabolic pathways, use the reverse reaction. Glycolysis, a catabolic pathway, uses the forward reaction. Aldolase is divided into two classes by mechanism. Applications: Carbon bond formation between dihydroxyacetone phosphate and linear aldehydes. Group: Enzymes. Synonyms: aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; Fructose-bisphosphate aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Enzyme Commission Number: EC 4.1.2.13. CAS No. 9024-52-6. Aldolase. Storage: Store at -20°C. Form: Frozen liquid. Source: Thermophillic bacteria. aldolase; fructose-1,6-bisphosphate triosephosphate-lyase; Fructose-bisphosphate aldolase; fructose diphosphate aldolase; D-fructose-1,6-bisphosphate D-glyceraldehyde-3-phosphate-lyase; EC 4.1.2.13; 9024-52-6. Cat No: NATE-1152. | |
| Native Lactate Dehydrogenase from Thermophillic bacteria | A lactate dehydrogenase (LDH or LD) is an enzyme found in nearly all living cells (animals, plants, and prokaryotes). LDH catalyzes the conversion of pyruvate to lactate and back, as it converts NADH to NAD+ and back. A dehydrogenase is an enzyme that transfers a hydride from one molecule to another. Applications: Diagnostic test and biosensors; nadh recycling. this enzyme is a potential candidate for biocatalysis, suitable for pharmaceutical development / manufacturing. Group: Enzymes. Synonyms: Lactate dehydrogenase; EC 1.1.1.27; LDH; LD. Enzyme Commission Number: EC 1.1.1.27. CAS No. 9001-60-9. LDH. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. Lactate dehydrogenase; EC 1.1.1.27; LDH; LD. Cat No: DIA-400. | |
| Native Malate dehydrogenase (Decarboxylating) from Thermophillic bacteria | Malate dehydrogenase is an enzyme in the citric acid cycle that catalyzes the conversion of malate into oxaloacetate (using NAD+) and vice versa (this is a reversible reaction). Malate dehydrogenase is not to be confused with malic enzyme, which catalyzes the conversion of malate to pyruvate producing NADPH. Malate dehydrogenase is also involved in gluconeogenesis, the synthesis of glucose from smaller molecules. Pyruvate in the mitochondria is acted upon by pyruvate carboxylase to form oxaloacetate, a citric acid cycle intermediate. In order to get the oxaloacetate out of the mitochondria, malate dehydrogenase reduces it to malate, and it then traverses ...; malate NAD dehydrogenase; NAD-dependent malate dehydrogenase; NAD-sp; ECific malate dehydrogenase; NAD-linked malate dehydrogenase; MDH; L-malate-NAD+ oxidoreductase; S-malate: NAD+ oxidoreductase; EC 1.1.1.38; Malate Dehydrogenase. Enzyme Commission Number: EC 1.1.1.38. CAS No. 9080-52-8. MDH. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. malic dehydrogenase; L-malate dehydrogenase; NAD-L-malate dehydrogenase; malic acid dehydrogenase; NAD-dependent malic dehydrogenase; NAD-malate dehydrogenase; NAD-malic dehydrogenase; malate NAD dehydrogenase; NAD-dependent malate dehydrogenase; NAD-sp; ECific malate dehydrogenase; NAD- | |
| Native Malate dehydrogenase from Thermophillic bacteria | Malate dehydrogenase is an enzyme in the citric acid cycle that catalyzes the conversion of malate into oxaloacetate (using NAD+) and vice versa (this is a reversible reaction). Malate dehydrogenase is not to be confused with malic enzyme, which catalyzes the conversion of malate to pyruvate producing NADPH. Malate dehydrogenase is also involved in gluconeogenesis, the synthesis of glucose from smaller molecules. Pyruvate in the mitochondria is acted upon by pyruvate carboxylase to form oxaloacetate, a citric acid cycle intermediate. In order to get the oxaloacetate out of the mitochondria, malate dehydrogenase reduces it to malate, and it then traverses the inner...e dehydrogenase; NAD-sp; ECific malate dehydrogenase; NAD-linked malate dehydrogenase; MDH; L-malate-NAD+ oxidoreductase; S-malate: NAD+ oxidoreductase; EC 1.1.1.37; Malate Dehydrogenase. Enzyme Commission Number: EC 1.1.1.37. CAS No. 9001-64-3. MDH. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. malic dehydrogenase; L-malate dehydrogenase; NAD-L-malate dehydrogenase; malic acid dehydrogenase; NAD-dependent malic dehydrogenase; NAD-malate dehydrogenase; NAD-malic dehydrogenase; malate NAD dehydrogenase; NAD-dependent malate dehydrogenase; NAD-sp; ECific malate dehydrogenase; NAD-linked malate dehydrogenase; MDH; L-malate-NAD+ oxidored | |
| Native Phosphofructokinase from Thermophillic bacteria | Phosphofructokinase is a kinase enzyme that phosphorylates fructose 6-phosphate in glycolysis. The enzyme-catalysed transfer of a phosphoryl group from ATP is an important reaction in a wide variety of biological processes. One enzyme that utilizes this reaction is phosphofructokinase (PFK), which catalyses the phosphorylation of fructose-6-phosphate to fructose-1,6-bisphosphate, a key regulatory step in the glycolytic pathway. PFK exists as a homotetramer in bacteria and mammals (where each monomer possesses 2 similar domains) and as an octomer in yeast (where there are 4 alpha-(PFK1) and 4 beta-chains (PFK2), the latter, like the mammalian monomers, possessing 2 similar domains). This protein may use the morpheein model of allosteric regulation. Applications: Diagnostic tests. Group: Enzymes. Synonyms: PFKWII; EC 2.7.1.11; PFK; phosphofructokinase; 6-phosphofructokinase; Phosphofructokinase I; Phosphohexokinase. Enzyme Commission Number: EC 2.7.1.11. CAS No. 9001-80-3. PFK. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. PFKWII; EC 2.7.1.11; PFK; phosphofructokinase; 6-phosphofructokinase; Phosphofructokinase I; Phosphohexokinase. Cat No: DIA-403. | |
| Native Pyruvate decarboxylase from Thermophillic bacteria | Pyruvate decarboxylase (PDC) is a homotetrameric enzyme that catalyses the decarboxylation of pyruvic acid to acetaldehyde and carbon dioxide in the cytoplasm. Pyruvate decarboxylase depends on cofactors thiamine pyrophosphate (TPP) and magnesium. PDC contains a β-α-β structure, yielding parallel β-sheets. Applications: C-c bond formation: ligation of two aldehyde molecules enantioselectively to 2-hydroxy ketones; preparation of (r)-phenylacetylcarbinol (pac). Group: Enzymes. Synonyms: Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Enzyme Commission Number: EC 4.1.1.1. CAS No. 9001-4-1. PDC. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Cat No: NATE-1159. | |
| Native Pyruvate Kinase from Thermophillic bacteria | Pyruvate kinase is an enzyme involved in glycolysis. It catalyzes the transfer of a phosphate group from phosphoenolpyruvate (PEP) to ADP, yielding one molecule of pyruvate and one molecule of ATP. Applications: Atp regeneration in biocatalysis. Group: Enzymes. Synonyms: Pyruvate kinase; EC 2.7.1.40; 9001-59-6; phosphoenolpyruvate kinase; phosphoenol transphosphorylase; pyruvate kinase (phosphorylating); fluorokinase; fluorokinase (phosphorylating); pyruvic kinase; pyruvate phosphotransferase; ATP:pyruvate 2-O-phosphotransferase. Enzyme Commission Number: EC 2.7.1.40. CAS No. 9001-59-6. Pyruvate Kinase. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. Pyruvate kinase; EC 2.7.1.40; 9001-59-6; phosphoenolpyruvate kinase; phosphoenol transphosphorylase; pyruvate kinase (phosphorylating); fluorokinase; fluorokinase (phosphorylating); pyruvic kinase; pyruvate phosphotransferase; ATP:pyruvate 2-O-phosphotransferase. Cat No: NATE-1158. | |
| Native Transketolase from Thermophillic bacteria | Transketolase is highly specific for ketol donor substrates and is stereospecific and enantioselective to hydroxyaldehyde substrates with an (R) configuration. It specifically catalyzes the irreversible transfer of one ketol unit from α-hydroxypyruvic acid to an aldehyde to produce a D-threo (3S,4R)ketose. Applications: This enzyme is a potential candidate for biocatalysis, suitable for pharmaceutical development / manufacturing. asymmetric c-c bond formation, ketol donor d-xylulose-5-phosphate may be substituted by hydroxypyruvate; preparation of ketose sugars such as fructose analogs, azasugars and fluorogenic substrates. Group: Enzymes. Synonyms: Transketolase; EC 2.2.1.1; 9014-48-6; glycolaldehydetransferase; Glycolaldehyde Transferase. Enzyme Commission Number: EC 2.2.1.1. CAS No. 9014-48-6. Transketolase. Storage: Store at -20°C. Form: Frozen Liquid. Source: Thermophillic bacteria. Transketolase; EC 2.2.1.1; 9014-48-6; glycolaldehydetransferase; Glycolaldehyde Transferase. Cat No: NATE-1162. | |
| Protocatechuate 3,4-Dioxygenase from Bacteria, Recombinant | In enzymology, a protocatechuate 3,4-dioxygenase (EC 1.13.11.3) is an enzyme that catalyzes the chemical reaction:3,4-dihydroxybenzoate + O2<-> 3-carboxy-cis,cis-muconate. Thus, the two substrates of this enzyme are 3,4-dihydroxybenzoate (protocatechuic acid) and O2, whereas its product is 3-carboxy-cis,cis-muconate. This enzyme belongs to the family of oxidoreductases, specifically those acting on single donors with O2 as oxidant and incorporation of two atoms of oxygen into the substrate (oxygenases). This enzyme participates in benzoate degradation via hydroxylation and 2,4-dichlorobenzoate degradation. It employs one cofactor, iron. Applications: Useful for removal of protocatechuate derived from choline esterase determination. Group: Enzymes. Synonyms: protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatech. Enzyme Commission Number: EC 1.13.11.3. CAS No. 9029-47-4. Protocatechuate 3, 4-dioxygenase. Mole weight: 28 kD α subuit, 24 kD β subunit?SDS-PAGE?. Activity: > 3 Units / mg. Storage: 1 - 10°C (do not freeze). Form: Solution. Source: E. coli. Species: Bacteria. protocatechuate 3,4-dioxygenase; protocatechuate oxygenase; protocatechuic acid oxidase; protocatechuic 3,4-dioxygenase; protocatechuic 3,4-oxygenase; 9029-47-4; EC 1.13.11.3; PCD. Cat No: NATE-1028. | |
| Tartrate,clinical detection,general bacteria tiny biochemical identification tube | Heterocyclic Organic Compound. CAS No. 104450-39-7. Molecular formula: C40H64N2O14. Mole weight: 796.941160 [g/mol]. Purity: 0.96. IUPACName: 2,3-dihydroxybutanedioic acid; 1-[4-[2-hydroxy-3- (propan-2-ylamino)propoxy]-3- (propoxymethyl)phenyl]ethanone. Catalog: ACM104450397. |  |
| Urea,clinical detection,nonferment bacteria | Heterocyclic Organic Compound. CAS No. 100078-01-1. Catalog: ACM100078011. | |
| Urease from Bacteria, Recombinant | Ureases, functionally, belong to the superfamily of amidohydrolases and phosphotriesterases. It is an enzyme that catalyzes the hydrolysis of urea into carbon dioxide and ammonia. The reaction occurs as follows: (NH2)2CO + H2O ? CO2 + 2NH3. Group: Enzymes. Synonyms: Urease. Enzyme Commission Number: EC 3.5.1.5. CAS No. 9002-13-5. Urease. Mole weight: 60.3 kD α subunit, 11.7 kD β subunit, 11.1 kD γ subunit?SDS-PAGE?. Activity: > 150 Units / mg. Storage: Below -20°C. Form: Lyophilized powder. Source: E. coli. Species: Bacteria. Urease. Cat No: NATE-1035. | |
| 10-Decarbamoyloxy-9-dehydromitomycin B | 10-Decarbamoyloxy-9-dehydromitomycin B is a mitane antibiotic produced by Streptomyces caespitosus KY 2072. It has anti-Gram-positive bacteria and anti-tumor cell activity. Synonyms: Mitomycin H; Azirino(2',3':3,4)pyrrolo(1,2-a)indole-4,7-dione, 1,1a,2,8,8a,8b-hexahydro-1,5-dimethyl-8a-hydroxy-6-methoxy-8-methylene-, (1aS-(1a-alpha,8a-alpha,8b-alpha))-. CAS No. 74148-44-0. Molecular formula: C15H16N2O4. Mole weight: 288.30. | |
| 10-Decarbomethoxyaclacinomycin A | 10-Decarbomethoxyaclacinomycin A is an anthracycline antibiotic produced by Streptomyces galilaeus MA144-Mlt mutant strain KE303. It has anti-tumor and gram-positive bacteria activity. Synonyms: 7-epi-10-Decarbomethoxyaclacinomycin A. CAS No. 76264-91-0. Molecular formula: C40H51NO13. Mole weight: 753.83. | |
| 10-Hydroxyundeca-2,4,6,8-tetraynamide | 10-Hydroxyundeca-2,4,6, 8-tetraynamide is a polyacetylene antibiotic produced by Mycena viridimarginata 7638. It has anti-gram-positive bacteria, negative bacteria, yeast, fungus activity and cytotoxicity. Synonyms: 10-Hydroxy-undeca-2,4,6,8-tetraynamide. CAS No. 83475-37-0. Molecular formula: C11H7NO2. Mole weight: 185.18. | |
| 1,11-Undecanedicarboxylic Acid | 1,11-Undecanedicarboxylic Acid is used in the synthesis of two Bis (tetra hydroisoquinoline) which were highly cytotoxic for cancer-cell cultures and less toxic to healthy cells and exhibited noticeable antimicrobial activity against Gram-positive and Gram-negative bacteria and fungal strain Candida albicans. Group: Biochemicals. Grades: Highly Purified. CAS No. 505-52-2. Pack Sizes: 2.5g, 5g. Molecular Formula: C13H24O4, Molecular Weight: 244.33. US Biological Life Sciences. |  Worldwide |
| 11-Bromo-1-undecene | 11-Bromo-1-undecene acts as a reagent used in the chemoenzymatic synthesis of macrolide antibiotics for the treatment of common bacteria infection. Group: Biochemicals. Grades: Highly Purified. CAS No. 7766-50-9. Pack Sizes: 500mg, 1g. Molecular Formula: C11H21Br, Molecular Weight: 233.19. US Biological Life Sciences. | Worldwide |
| 11-Deoxy-13-deoxodaunorubicin | 11-Deoxy-13-deoxodaunorubicin is an anthracycline antibiotic produced by Micromonospora peucetica B211 F.I. It has anti-gram-positive bacteria, negative bacteria and tumor activity. CAS No. 71800-92-5. Molecular formula: C27H31NO8. Mole weight: 497.54. | |
| 11-Deoxy-13-dihydrodaunorubicin | 11-Deoxy-13-dihydrodaunorubicin is an anthracycline antibiotic produced by Microjnonospora peucetica B211 F. I. It has anti-gram-positive bacteria, negative bacteria and tumor activity. CAS No. 71800-90-3. Molecular formula: C27H31NO9. Mole weight: 513.54. | |
| 11-Hydroxynovobiocin | 11-Hydroxynovobiocin is a novobiocin homolog produced by Sebekia benihana UC 5762 (NRRL 11111). It has anti-gram-negative bacteria effect, and its activity is equivalent to 30% of novobiocin. Molecular formula: C31H36N2O12. Mole weight: 628.62. | |
| 1,2:3,4:5,6-Tri-O-isopropylidene-L-glycero-L-gulo-heptitol | 1,2:3,4:5,6-Tri-O-isopropylidene-L-glycero-L-gulo-heptitol, a multifaceted biomedicine, unveils extraordinary potential in the realm of medicine. With striking antimicrobial properties, it displays efficaciousness against drug-resistant bacteria and fungal infections, heralding a new era of combatting formidable pathogens. The distinctive structure and pharmacological properties of this compound ignite a fervor for further research and development in the biomedical frontier, propelling the evolution of healthcare for mankind. Molecular formula: C16H28O7. Mole weight: 332.39. | |
| 1,2,3,4-Tetra-O-benzoyl-D-glucopyranose-13C6 | Used in the preparation of α-Glycosphingolipids, important in the innate-type immune response to Gram-negative bacteria. Group: Biochemicals. Alternative Names: 1,2,3,4-Tetrabenzoate-D-glucopyranose. Grades: Highly Purified. Pack Sizes: 250mg. US Biological Life Sciences. | Worldwide |
| 1,2,4,5-Tetrachlorobenzene-13C6 | 1,2,4,5-Tetrachlorobenzene-13C6 is an intermediate used in the synthesis of 2,4,5-Trichlorophenol-13C6 (T774148), which is an isotope labelled 2,4,5-Trichlorophenol is used as a broad range pesticide against insects, fungi, vegetation and bacteria. It has become a common environmental contaminant and probable human carcinogen. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: 13C6H2Cl4, Molecular Weight: 221.85. US Biological Life Sciences. | Worldwide |
| 1,2,4,6-Tetra-O-acetyl-3-deoxy-3-N-(4-nitrobenzamido)-D-galactopyranose | 1,2,4,6-Tetra-O-acetyl-3-deoxy-3-N-(4-nitrobenzamido)-D-galactopyranose, identified as a chemical entity of paramount significance, assumes a critical role in augmenting the development of antibiotics as an efficacious remedy to counter bacterial infections. With a proclivity for serving as a precursor for the synthesis of aminoglycoside antibiotics, such as kanamycin and amikacin, it exhibits promise in the race for combating pernicious bacteria and thwarting their detrimental effects on the human body. Synonyms: (3R,4S,5R,6R)-6-(Acetoxymethyl)-4-(4-nitrobenzamido)tetrahydro-2H-pyran-2,3,5-triyl triacetate; 947590-43-4. CAS No. 947590-43-4. Molecular formula: C21H24N2O12. Mole weight: 496.42. | |
| 1,2,4,6-Tetra-O-acetyl-3-deoxy-D-glucopyranose | 1,2,4,6-Tetra-O-acetyl-3-deoxy-D-glucopyranose, a pivotal compound found in the biomedicine sector, holds immense significance in the synthesis of diverse pharmaceuticals, particularly those designed to combat metabolic disorders and infectious ailments. This compound showcases noteworthy antiviral and antibacterial attributes, contributing significantly to the creation of therapeutic remedies targeting viral infections and antibiotic-resistant bacteria. Synonyms: 3-Deoxy-1,2,4,6-tetra-O-acetyl-D-glucopyranose. CAS No. 5040-9-5. Molecular formula: C14H20O9. Mole weight: 332.3. | |
| 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate dehydrogenase | Involved in the o-xylene degradation pathway in bacteria. Group: Enzymes. Enzyme Commission Number: EC 1.3.1.68. 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-1336; 1,2-dihydroxy-6-methylcyclohexa-3,5-dienecarboxylate dehydrogenase; EC 1.3.1.68. Cat No: EXWM-1336. | |
| 1,2-Dimyristoyl-sn-glycero-3-phosphocholine | 1,2-Dimyristoyl-sn-glycero-3-phosphocholine is used in the generation of micelles and liposomes.1,2-Dimyristoyl-sn-glycero-3-phosphocholine (DMPC) is a phospholipid found in eukaryotes, but not most bacteria. It is used in lipid bilayer studies to analyze organelle and cell membranes. Its also been used to study molecules in membranes, such as the interaction between DMPC and proteins in lab-constructed dimyristoyl phosphatidyl choline vesicles.CAS Number:18194-24-6. Group: Biochemicals. Alternative Names: 3,5,9-Trioxa-4-phosphatricosan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxotetradecyl)oxy]-, hydroxide, inner salt, 4-oxide, (R)-; Choline, hydroxide, dihydrogen phosphate, inner salt, ester with 1,2-dimyristin, L- (8CI); Choline, phosphate, ester with L-1,2-dimyristin(6CI); 1,2-Bis(myristoyl)-sn-glycerophosphocholine; 1,2-Dimyristoyl-3-sn-phosphatidylcholine; 1,2-Dimyristoyl-3-sn-phosphatidylcholine; 1,2-Dimyristoyl-L-3-phosphatidylcholine; 1,2-Dimyristoyl-L-phosphatidylcholine; 1,2-Dimyristoyl-L-a-phosphatidylcholine; 1,2-Dimyristoyl-sn-3-glycerophosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphatidylcholine; 1,2-Dimyristoyl-sn-glycero-3-phosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphocholine; 1,2-Dimyristoyl-sn-glycero-3-phosphorylcholine; 1,2-Dimyristoyl-sn-glycerol-3. Grades: Highly Purified. CAS No. 18194-24-6. Pack Sizes: 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-N-phthalimido-a-D-glucopyranose | 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-N-phthalimido-a-D-glucopyranose, a chemical compound utilized in the production of glycopeptide antibiotics, demonstrates its functional potential as an acyl donor in the course of synthesizing vancomycin derivatives. Resistant against MRSA and other drug-resistance bacteria, said derivatives showcase their potential to alleviate the issues precipitated by such pathogens. Synonyms: 1,3,4,6-Tetraacetyl-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-a-D-glucopyranose. CAS No. 31505-44-9. Molecular formula: C22H23NO11. Mole weight: 477.42. | |
| 1,3,6,8-tetrahydroxynaphthalene synthase | Isolated from the fungus Colletotrichum lagenarium, and the bacteria Streptomyces coelicolor and Streptomyces peucetius. It only uses malonyl-CoA, without invovement of acetyl-CoA. Group: Enzymes. Synonyms: PKS1; THNS; SCO1206; RppA. Enzyme Commission Number: EC 2.3.1.233. 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-2181; 1,3,6,8-tetrahydroxynaphthalene synthase; EC 2.3.1.233; PKS1; THNS; SCO1206; RppA. Cat No: EXWM-2181. | |
| 13-Deoxycarminomycin | 13-Deoxycarminomycin, an antineoplastic agent and a bacterial metabolite, is a cytotoxic anthracycline antibiotic produced by Streptomyces peucetius var. carminatus (a biochemical mutant of Streptomyces peucetius var. caesius). It has activity against Gram-positive bacteria, Gram-negative bacteria, tumors and P-388 murine leukemia. Synonyms: Antibiotic D 788-11; R 20X; 13-Deoxocarminomycin; (8S)-10α-[(3-Amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-1,6,8α,11-tetrahydroxy-5,12-naphthacenedione; 13-Deoxocarminomycin I; (1S,3S)-3-Ethyl-3,5,10,12-tetrahydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-tetracenyl 3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranoside; 5,12-Naphthacenedione, 7,8,9,10-tetrahydro-10-((3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy)-8-ethyl-1,6,8,11-tetrahydroxy-, (8S-cis)-; 5,12-Naphthacenedione, 10-[(3-amino-2,3,6-trideoxy-α-L-lyxo-hexopyranosyl)oxy]-8-ethyl-7,8,9,10-tetrahydro-1,6,8,11-tetrahydroxy-, (8S,10S)-. Grades: ≥95%. CAS No. 76034-18-9. Molecular formula: C26H29NO9. Mole weight: 499.51. | |
| 13-deoxydaunorubicin hydroxylase | The enzymes from the Gram-positive bacteria Streptomyces sp. C5 and Streptomyces peucetius show broad substrate specificity for structures based on an anthracycline aglycone, but have a strong preference for 4-methoxy anthracycline intermediates (13-deoxydaunorubicin and 13-dihydrodaunorubicin) over their 4-hydroxy analogues (13-deoxycarminomycin and 13-dihydrocarminomycin), as well as a preference for substrates hydroxylated at the C-13 rather than the C-14 position. Group: Enzymes. Synonyms: DoxA. Enzyme Commission Number: EC 1.14.13.181. 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-0780; 13-deoxydaunorubicin hydroxylase; EC 1.14.13.181; DoxA. Cat No: EXWM-0780. | |
| 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-amine | 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-amine is a boron compound that can potentially be used for treatment of periodontal disease such as infection involving bacteria, viruses, fungi and/or parasites. 1,3-Dihydro-1-hydroxy-2,1-benzoxaborol-5-amine may also be used as an anti-inflammatory agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 947165-26-6. Pack Sizes: 5mg, 10mg. Molecular Formula: C7H8BNO2, Molecular Weight: 148.949999999999. US Biological Life Sciences. | Worldwide |
| 1,3-Naphthalenediol | 1,3-Naphthalenediol is a derivative of naphthalene (N345600) and may have antibacterial activity against oral bacteria. Group: Biochemicals. Grades: Highly Purified. CAS No. 132-86-5. Pack Sizes: 500mg, 1g. Molecular Formula: C10H8O2, Molecular Weight: 160.169999999999. US Biological Life Sciences. | Worldwide |
| 13-O-Ethylamphotericin B | 13-O-Ethylamphotericin B is an analogue of 13-O-Methylamphotericin B, an antifungal. 13-O-Methylamphotericin B is a derivative of Amphotericin B, a polypeptide antibiotic active against gram positive bacteria. Antifungal. Synonyms: (1R, 3S, 5R, 6R, 9R, 11R, 15S, 16R, 17R, 18S, 19E, 21E, 23E, 25E, 27E, 29E, 31E, 33R, 35S, 36R, 37S)-33-(((2R, 3S, 4S, 5S, 6R)-4-Amino-3, 5-dihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-1-ethoxy-3, 5, 6, 9, 11, 17, 37-heptahydroxy-15, 16, 18-trimethyl-13-oxo-14, 39-dioxabicyclo[33.3.1]nonatriaconta-19, 21, 23, 25, 27, 29, 31-heptaene-36-carboxylic Acid. Molecular formula: C49H77NO17. Mole weight: 952.13. | |
| 13-O-Ethylamphotericin B | 13-O-Ethylamphotericin B is an analogue of 13-O-Methylamphotericin B (M287440), an antifungal. 13-O-Methylamphotericin B is a derivative of Amphotericin B (A634250), a polypeptide antibiotic active against gram positive bacteria. Antifungal. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C49H77NO17, Molecular Weight: 952.13. US Biological Life Sciences. | Worldwide |
| 13-O-Methylamphotericin B | 13-O-Methylamphotericin B is an antifungal. 13-O-Methylamphotericin B is a derivative of Amphotericin B (A634250), a polypeptide antibiotic active against gram positive bacteria. Antifungal. Group: Biochemicals. Grades: Highly Purified. CAS No. 136135-57-4. Pack Sizes: 5mg, 50mg. Molecular Formula: C48H75NO17. US Biological Life Sciences. | Worldwide |
| 13-O-Methylamphotericin B | 13-O-Methylamphotericin B is an antifungal. 13-O-Methylamphotericin B is a derivative of Amphotericin B, a polypeptide antibiotic active against gram positive bacteria. Antifungal. Synonyms: 14,39-Dioxabicyclo[33.3.1]nonatriacontane Amphotericin B derivative. CAS No. 136135-57-4. Molecular formula: C48H75NO17. Mole weight: 938.11. | |
| 1,4-Anhydro-D-erythritol | 1,4-Anhydro-D-erythritol, a versatile sugar alcohol, is employed in the synthesis of a plethora of compounds, from biodegradable plastics to pharmaceuticals. The potential scope of its applications extends towards the therapeutic treatment of diabetes, owing to its hypoglycemic effects. Its antimicrobial properties have been extensively scrutinized, with studies targeting its potential employment in countering streptococcal bacteria responsible for dental caries. Synonyms: 1,4-Anhydroerythritol; cis-Tetrahydrofuran-3,4-diol; (3R,4S)-tetrahydrofuran-3,4-diol; (3R,4S)-oxolane-3,4-diol; 1,4-Anhydro-D-erythritol; Erythritan; (-)-1,4-ANHYDRO-L-THREITOL; (3~{S},4~{R})-oxolane-3,4-diol; 3,4-Furandiol, tetrahydro-, (3R,4S)-rel-; cis-3,4-Dihydroxytetrahydrofuran; MFCD00075210; cis-3,4-Tetrahydrofurandiol; SCHEMBL196429; 1 pound not4-Anhydroerythritol; 1,4-Anhydroerythritol, 95%; SSYDTHANSGMJTP-ZXZARUISSA-N; DTXSID401318325; AMY16786; (3R, 4S)-tetrahydrofuran-3,4-diol; AKOS016011113; AS-33974; CS-0049648; EN300-195706; P15622; A872684; IJ8. CAS No. 4358-64-9. Molecular formula: C4H8O3. Mole weight: 104.10. | |
| 1,4-dihydroxy-2-naphthoyl-CoA synthase | This enzyme is involved in the synthesis of 1,4-dihydroxy-2-naphthoate, a branch point metabolite leading to the biosynthesis of menaquinone (vitamin K2, in bacteria), phylloquinone (vitamin K1 in plants), and many plant pigments.The coenzyme A group is subsequently removed from the product by EC 3.1.2.28, 1,4-dihydroxy-2-naphthoyl-CoA hydrolase. Group: Enzymes. Synonyms: naphthoate synthase; 1,4-dihydroxy-2-naphthoate synthase; dihydroxynaphthoate synthase; o-succinylbenzoyl-CoA 1,4-dihydroxy-2-naphthoate-lyase (cyclizing); MenB; o-succinylbenzoyl-CoA dehydratase (cyclizing). Enzyme Commission Number: EC 4.1.3.36. CAS No. 61328-42-5. 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-4913; 1,4-dihydroxy-2-naphthoyl-CoA synthase; EC 4.1.3.36; 61328-42-5; naphthoate synthase; 1,4-dihydroxy-2-naphthoate synthase; dihydroxynaphthoate synthase; o-succinylbenzoyl-CoA 1,4-dihydroxy-2-naphthoate-lyase (cyclizing); MenB; o-succinylbenzoyl-CoA dehydratase (cyclizing). Cat No: EXWM-4913. | |
| 1,4-D-Xylobiose | 1,4-D-Xylobiose is a vital substance used in the biomedical industry. It exhibits potential applications as a dietary supplement due to its prebiotic properties. It can serve as a nutrition source for beneficial gut bacteria, promoting a healthy intestinal environment. Synonyms: β1,4-D-Xylobiose; 4-O-(b-D-Xylopyranosyl)-D-xylopyranose; 1,4-β-Xylobiose; 4-O-β-D-Xylopyranosyl-D-xylose; Xylobiose. Grades: ≥98%. CAS No. 6860-47-5. Molecular formula: C10H18O9. Mole weight: 282.25. | |
| 1,5-Anhydro-2,3-dideoxy-2-(N2-isobutyrylguanidin-1-yl)-D-glucitol | 1,5-Anhydro-2,3-dideoxy-2-(N2-isobutyrylguanidin-1-yl)-D-glucitol: An intriguing compound with notable promise, this product elicits immense interest in the biomedical field. Its remarkable therapeutic potential shines in its ability to combat drug-resistant bacteria and various associated infections. Unlocking its full capabilities requires meticulous examination of scholarly works and insights from authoritative experts, as it holds immense potential for diverse application domains. Molecular formula: C15H21N5O5. Mole weight: 351.37. | |
| 15-Hydroxypentadecanoic acid | 15-Hydroxypentadecanoic acid is a long-chain fatty acid found in various plant and animal sources and also produced by bacteria and fungi. It has potential health benefits and is used as an intermediate in the synthesis of other organic compounds, including pharmaceuticals, agrochemicals and surfactants. Its unique chemical properties make it an essential ingredient in several industrial processes, especially in the fields of food science and nutrition. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 4617-33-8. Pack Sizes: 1 g. Product ID: HY-W105734. | |
| 16,17-Dehydrorifamycin G | 16,17-Dehydrorifamycin G is an antibiotic produced by Nocardia mediterranei R-21 (DSM 1415). It has anti-Gram-positive bacteria and weak anti-Gram-negative bacteria activity. Molecular formula: C36H45NO12. Mole weight: 683.74. | |
| 1,6:2,3-Dianhydro-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-mannopyranose | Purportedly an efficacious chemical in inhibiting the pathological propagation of bacteria and viruses, 1,6:2,3-Dianhydro-4-O-(2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl)-b-D-mannopyranose is a vital substance involved in the biomedical field. Its mechanism of action involves significantly impeding the growth and spreading of deleterious microorganisms within the human body, resulting in the treatment and prevention of bacterial and viral infections. Synonyms: SCHEMBL18045633; (2S,3R,4S,5R,6R)-2-(((1R,2S,4S,5R,6R)-3,8,9-Trioxatricyclo[4.2.1.02,4]nonan-5-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate; 103702-87-0. CAS No. 103702-87-0. Molecular formula: C20H26O13. Mole weight: 474.41. | |
| 1,6-Anhydro-b-D-cellopentose | 1,6-Anhydro-b-D-cellopentose is a molecular structure extensively used in research into antibacterial substances and new antibiotic drugs. It mainly works in the study of diseases caused by antibiotic-resistant bacteria. Synonyms: Cellopentaosan. CAS No. 122274-98-0. Molecular formula: C30H50O25. Mole weight: 810.70. | |
| 1,6-Anhydro-b-D-galactopyranose | 1,6-Anhydro-b-D-galactopyranose is a reducing sugar often used in biomedical research. As a gibberellin biosynthesis inhibitor, it is commonly utilized in the study of plant growth regulation and hormone synthesis. Additionally, it aids in the analysis of and insight into the carbohydrate structure-function relationships in bacteria and fungi. Synonyms: 6,8-Dioxa-bicylo[3,2,1]octonae-2,3,4-triol; D-Galactosan. CAS No. 644-76-8. Molecular formula: C6H10O5. Mole weight: 162.14. | |
| 16-Deethylindanomycin | 16-Deethylindanomycin is an antibiotic of the indanomycin group produced by Streptomyces setonii. It has anti-gram-positive bacteria and coccidia activity. Synonyms: Omomycin; 2H-Pyran-2-acetic acid, tetrahydro-alpha,5-dimethyl-6-(1-ethyl-4-(2,3,3a,4,5,7a-hexahydro-4-(1H-pyrrol-2-ylcarbonyl)-1H-inden-5-yl)-1,3-butadienyl)-, (3aR-(3a-alpha,4-alpha,5-alpha(1E(2R*(R*),5S*,6R*),3E),7a-beta))-. Grades: ≥95%. CAS No. 106803-22-9. Molecular formula: C29H39NO4. Mole weight: 465.62. | |
| 17-Hydroxyventuricidin A | Antifungal. Antibacterial against Gram-positive bacteria. Group: Biochemicals. Alternative Names: Antibiotic YP 02259L-C. Grades: Highly Purified. CAS No. 113204-43-6. Pack Sizes: 250ug, 1mg. Molecular Formula: C41H67NO12. US Biological Life Sciences. | Worldwide |
| 1,8-Dichloroanthraquinone | 1,8-Dichloroanthraquinone, an anthraquinone, is an inhibitor of sulfide production by sulfate-reducing bacteria [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 82-43-9. Pack Sizes: 25 g; 50 g; 100 g; 500 g. Product ID: HY-W103170. | |
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