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Phenazine. Group: Electroluminescence materials organic light-emitting diode (oled) materials other materials. Alternative Names: Dibenzopyrazine. CAS No. 92-82-0. Pack Sizes: 10 g in glass bottle. Product ID: phenazine. Molecular formula: 180.20. Mole weight: C12H8N2. c1ccc2nc3ccccc3nc2c1. 1S/C12H8N2/c1-2-6-10-9 (5-1)13-11-7-3-4-8-12 (11)14-10/h1-8H, PCNDJXKNXGMECE-UHFFFAOYSA-N. PCNDJXKNXGMECE-UHFFFAOYSA-N.
Phenazine
Phenazine is an electron shuttles, which modulates the redox state of cells and the downstream gene expression related to biofilm formation and bacterial survival. Phenazines is a biocontrol agents, which affects the growth of plants and induces the systemic resistance in plants [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 92-82-0. Pack Sizes: 10 mM * 1 mL; 10 g; 25 g; 50 g; 100 g. Product ID: HY-W016477.
Phenazine,1,2,3,4,6,7-hexahydro-(9ci)
Heterocyclic Organic Compound. CAS No. 112448-71-2. Catalog: ACM112448712.
phenazine-1-carboxylate N-methyltransferase
The enzyme, characterized from the bacterium Pseudomonas aeruginosa, is involved in the biosynthesis of pyocyanin, a toxin produced and secreted by the organism. The enzyme is active in vitro only in the presence of EC 1.14.13.218, 5-methylphenazine-1-carboxylate 1-monooxygenase. Group: Enzymes. Synonyms: phzM (gene name). Enzyme Commission Number: EC 2.1.1.327. 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-1935; phenazine-1-carboxylate N-methyltransferase; EC 2.1.1.327; phzM (gene name). Cat No: EXWM-1935.
Phenazine-1-carboxylic acid
Phenazine-1-carboxylic acid is an antifungal agent. Additionally, Phenazine-1-carboxylic acid exhibits anticancer activity by inducing apoptosis in cancer cells through the regulation of ROS generation. Phenazine-1-carboxylic acid can upregulate the expression of IL-8 and ICAM-1 while inhibiting the release of RANTES and MCP-1, demonstrating its potential immunomodulatory effects. Phenazine-1-carboxylic acid holds significant research value in the areas of anti-infection, anticancer, and immune response modulation [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 2538-68-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 1 g. Product ID: HY-33037.
Phenazine Ethosulfate is an intermediate which is used to detect nitric oxide reducatase activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 10510-77-7. Pack Sizes: 250mg, 500mg. Molecular Formula: C14H13N2 C2H5O4S, Molecular Weight: 209.271251199999. US Biological Life Sciences.
Worldwide
Phenazine methosulfate
25g Pack Size. Group: Biochemicals. Formula: C14H14N2O4S. CAS No. 299-11-6. Prepack ID 20097670-25g. Molecular Weight 306.34. See USA prepack pricing.
Phenazine methosulfate 99+% (HPLC)
Phenazine methosulfate 99+% (HPLC). Group: Biochemicals. Alternative Names: 5-Methylphenazinium methyl sulfate; N-Methylphenazonium methyl sulfate. Grades: Highly Purified. CAS No. 299-11-6. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences.
Worldwide
Phenazine methylsulfate
Phenazine methylsulfate is a free radical generator that can act as an electron transfer reactant in cell viability assays. It also has insecticidal properties. Furthermore, Phenazine methylsulfate induces oxidative DNA damage and cell apoptosis , showing antitumor activity [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 5-Methylphenazinium methylsulfate. CAS No. 299-11-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-W004520.
1,6-Dihydroxy-2-chlorophenazine
It is produced by the strain of Streptosporangium sp. 1656. It has weak anti-fungal and anti-yeast activity. Synonyms: 1,6-Phenazinediol, 2-chloro-; 7-chloro-6-hydroxy-5H-phenazin-1-one; 7-chloro-6-hydroxyphenazin-1(5H)-one. Grades: >95%. CAS No. 93768-40-2. Molecular formula: C12H7N2O2Cl. Mole weight: 246.65.
1,6-Dihydroxyphenazine
It is produced by the strain of Streptomyces thioluteus M6-62a. It mainly has the antifungal effect, also has the inhibitory effect against the human type tuberculosis bacillus. Synonyms: 1,6-Phenazinediol; 6-hydroxyphenazin-1(5h)-one; 6-hydroxy-5H-phenazin-1-one; 2,5-diMethoxylnaphthalene. Grades: ≥95%. CAS No. 69-48-7. Molecular formula: C12H8N2O2. Mole weight: 212.20.
1,6-Dimethoxy-phenazine
It is a simple phenazine produced by several species of streptomyces. It is a weakly active antibacterial metabolite with activity against Sarcina lutea and mycobacteria. Dimethoxyphenazine and related phenazines are important dereplication standards in discovery research to eliminate leads due to high amounts of weakly potent actives. Synonyms: Crystalloiodinine B. Grades: >98% by HPLC. CAS No. 13398-79-3. Molecular formula: C14H12N2O2. Mole weight: 240.26.
2,3-Phenazinediamine is used for the study on detection of HIV-1 p24 antigen in patients with varying degrees of viremia using ELISA with photochemical signal amplication system. Group: Biochemicals. Grades: Highly Purified. CAS No. 655-86-7. Pack Sizes: 1g, 5g. Molecular Formula: C12H10N4, Molecular Weight: 210.23. US Biological Life Sciences.
Worldwide
2,3-Phenazinediol
2,3-Phenazinediol is a reactant used in the preparation of anticancer agents. Antibacterial agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 19220-18-9. Pack Sizes: 500mg, 1g. Molecular Formula: C12H8N2O2. US Biological Life Sciences.
The enzyme is involved in the biosynthesis of prenylated phenazines by the bacterium Streptomyces anulatus. It is specific for both dimethylallyl diphosphate and 5,10-dihydrophenazine-1-carboxylate. Group: Enzymes. Synonyms: PpzP; dihydrophenazine-1-carboxylate dimethylallyltransferase; 5,10-dihydrophenazine 1-carboxylate dimethylallyltransferase. Enzyme Commission Number: EC 2.5.1.121. 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-2737; 5,10-dihydrophenazine-1-carboxylate 9-dimethylallyltransferase; EC 2.5.1.121; PpzP; dihydrophenazine-1-carboxylate dimethylallyltransferase; 5,10-dihydrophenazine 1-carboxylate dimethylallyltransferase. Cat No: EXWM-2737.
5-methylphenazine-1-carboxylate 1-monooxygenase
The enzyme, characterized from the bacterium Pseudomonas aeruginosa, is involved in the biosynthesis of pyocyanin, a toxin produced and secreted by the organism. It can also act on phenazine-1-carboxylate, converting it into phenazin-1-ol. Group: Enzymes. Synonyms: phzS (gene name). Enzyme Commission Number: EC 1.14.13.218. 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-0820; 5-methylphenazine-1-carboxylate 1-monooxygenase; EC 1.14.13.218; phzS (gene name). Cat No: EXWM-0820.
6,9-Dimethoxy-phenazine-1-carboxylic acid
Heterocyclic Organic Compound. Alternative Names: 6,9-DIMETHOXY-PHENAZINE-1-CARBOXYLIC ACID. CAS No. 103942-91-2. Molecular formula: C15H12N2O4. Mole weight: 284.27. Catalog: ACM103942912.
7-Methyl-phenazine-1-carboxylic acid
Heterocyclic Organic Compound. Alternative Names: 7-METHYL-PHENAZINE-1-CARBOXYLIC ACID. CAS No. 103942-88-7. Molecular formula: C14H10N2O2. Mole weight: 238.24. Catalog: ACM103942887.
Dipyrido[3,2-a:2',3'-c]phenazine. Group: Ligands for functional metal complexes. Alternative Names: Dipyridoacphenazinehemihydratemin. CAS No. 19535-47-8. Product ID: quinoxalino[2,3-f][1,10]phenanthroline. Molecular formula: 282.30. Mole weight: C18H10N4. C1=CC=C2C (=C1)N=C3C4=C (C5=C (C3=N2)C=CC=N5)N=CC=C4. BVQAWSJMUYMNQN-UHFFFAOYSA-N. InChI=1S/C18H10N4/c1-2-8-14-13 (7-1)21-17-11-5-3-9-19-15 (11)16-12 (18 (17)22-14)6-4-10-20-16/h1-10H. 98%.
Endophenazine A
It is produced by the strain of Streptomyces anulatus. It has activity against gram-positive bacteria and filamentous fungi such as mucor and Penicillium. Its weeding ability to Lemna minor is relatively low. Synonyms: 1-Phenazinecarboxylic acid, 9-(3-methyl-2-butenyl)-; 9-(3-Methyl-2-buten-1-yl)-1-phenazinecarboxylic Acid. CAS No. 86125-71-5. Molecular formula: C18H16N2O2. Mole weight: 292.33.
Endophenazine B
It is produced by the strain of Streptomyces anulatus. It's a phenazine antibiotic, and it has low herbicidal activity against Lemna minor. Synonyms: 5,7-Dihydro-5-methyl-9-(3-methyl-2-buten-1-yl)-7-oxo-1-phenazinecarboxylic Acid. CAS No. 479415-40-2. Molecular formula: C19H18N2O3. Mole weight: 322.36.
Methanosarcina-phenazine hydrogenase
Contains nickel, iron-sulfur clusters and cytochrome b. The enzyme from some sources contains selenocysteine. Group: Enzymes. Synonyms: methanophenazine hydrogenase; methylviologen-reducing hydrogenase. Enzyme Commission Number: EC 1.12.98.3. CAS No. 9027-5-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0526; Methanosarcina-phenazine hydrogenase; EC 1.12.98.3; 9027-05-8; methanophenazine hydrogenase; methylviologen-reducing hydrogenase. Cat No: EXWM-0526.
An impurity of Perphenazine which is a typical antipsychotic used to treat psychosis. Synonyms: 4-(3-Phenothiazin-10-ylpropyl)-1-piperazineethanol; 10-[3-[4-(2-Hydroxyethyl)-1-piperazinyl]propyl]-10H-phenothiazine; 4-[3-(10H-Phenothiazin-10-yl)propyl]-1-piperazineethanol; Phenazine (Pharmaceutical); Perphenazine EP Impurity B. Grades: > 95%. CAS No. 3533-97-9. Molecular formula: C21H27N3OS. Mole weight: 369.53.
10-(4-Chlorophenyl)-3-[(4-chlorophenyl)amino]-2(10H)-phenazinone was used in the biological study to observe the pro-oxidative activity of dihydrophenazines in neutrophils of humans. Group: Biochemicals. Grades: Highly Purified. CAS No. 90712-89-3. Pack Sizes: 1mg, 5mg. Molecular Formula: C24H15Cl2N3O, Molecular Weight: 432.3. US Biological Life Sciences.
Worldwide
2-[(2-Bromophenyl)amino]-3-nitrobenzoic Acid
2-[(2-Bromophenyl)amino]-3-nitrobenzoic Acid is an intermediate in the synthesis of Endophenazine A which is a new phenazine antibiotic isolated from the arthropod associated endosymbiont Streptomyces anulatus and shows antimicrobial activities against Gram-positive bacteria and some filamentous fungi, and herbicidal activity against Lemna minor (duckweed). Group: Biochemicals. Grades: Highly Purified. CAS No. 38120-57-9. Pack Sizes: 5mg, 100mg. Molecular Formula: C13H9BrN2O4, Molecular Weight: 337.13. US Biological Life Sciences.
Worldwide
2-[(2-Chlorophenyl)amino]-3-nitrobenzoic Acid
2-[(2-Chlorophenyl)amino]-3-nitrobenzoic Acid is an intermediate in the synthesis of Endophenazine A which is a new phenazine antibiotic isolated from the arthropod associated endosymbiont Streptomyces anulatus and shows antimicrobial activities against Gram-positive bacteria and some filamentous fungi, and herbicidal activity against Lemna minor (duckweed). Group: Biochemicals. Grades: Highly Purified. CAS No. 38120-54-6. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C13H9ClN2O4, Molecular Weight: 292.67. US Biological Life Sciences.
Worldwide
2-amino-4-deoxychorismate synthase
Requires Mg2+. The reaction occurs in the reverse direction to that shown above. In contrast to most anthranilate-synthase I (ASI) homologues, this enzyme is not inhibited by tryptophan. In Streptomyces globisporus, the sequential action of this enzyme and EC 1.3.99.24, 2-amino-4-deoxychorismate dehydrogenase, leads to the formation of the benzoxazolinate moiety of the enediyne antitumour antibiotic C-1027.In certain Pseudomonads the enzyme participates in the biosynthesis of phenazine, a precursor for several compounds with antibiotic activity. Group: Enzymes. Synonyms: ADIC synthase; 2-amino-2-deoxyisochorismate synthase;SgcD. Enzyme Commission Number: EC 2.6.1.86. 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-2927; 2-amino-4-deoxychorismate synthase; EC 2.6.1.86; ADIC synthase; 2-amino-2-deoxyisochorismate synthase;SgcD. Cat No: EXWM-2927.
3-Amino-2-phenazinol Hydrochloride (~90%)
3-Amino-2-phenazinol is a reagent used in the synthesis of phenazine derivatives which are potential antibacterial and antifungal agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 4569-77-1. Pack Sizes: 100mg, 250mg. Molecular Formula: C12H9N3O; (HCl). US Biological Life Sciences.
4-(3-Phenothiazin-10-ylpropyl)-1-piperazineethanol-d8. Group: Biochemicals. Alternative Names: 10-[3-[4-(2-Hydroxyethyl)-1-piperazinyl]propyl]-10H-phenothiazine-d8; 4-[3-(10H-Phenothiazin-10-yl)propyl]-1-piperazineethanol-d8; Phenazine-d8 (Pharmaceutical). Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C21H19D8N3OS, Molecular Weight: 377.57. US Biological Life Sciences.
Worldwide
4-methylphenol dehydrogenase (hydroxylating)
A flavocytochrome c (FAD). Phenazine methosulfate can act as acceptor. A quinone methide is probably formed as intermediate. The first hydroxylation forms 4-hydroxybenzyl alcohol; a second hydroxylation converts this into 4-hydroxybenzaldehyde. Group: Enzymes. Synonyms: p-cresol-(acceptor) oxidoreductase (hydroxylating); p-cresol methylhydroxylase; 4-cresol dehydrogenase (hydroxylating). Enzyme Commission Number: EC 1.17.99.1. CAS No. 66772-07-4. 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-1101; 4-methylphenol dehydrogenase (hydroxylating); EC 1.17.99.1; 66772-07-4; p-cresol-(acceptor) oxidoreductase (hydroxylating); p-cresol methylhydroxylase; 4-cresol dehydrogenase (hydroxylating). Cat No: EXWM-1101.
5,10-dihydrophencomycin methyl ester
It has very weak activity against Escherichia coli and Bacillus subtilis. Synonyms: 5,10-Dihydro-1,6-phenazinedicarboxylic acid dimethyl ester. CAS No. 193421-85-1. Molecular formula: C16H14N2O4. Mole weight: 298.29.
alcohol dehydrogenase (azurin)
A soluble, periplasmic PQQ-containing quinohemoprotein. Also contains a single heme c. Occurs in Comamonas and Pseudomonas. Does not require an amine activator. Oxidizes a wide range of primary and secondary alcohols, and also aldehydes and large substrates such as sterols; methanol is not a substrate. Usually assayed with phenazine methosulfate or ferricyanide. Like all other quinoprotein alcohol dehydrogenases it has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ. Group: Enzymes. Synonyms: type II quinoprotein alcohol dehydrogenase; quinohaemoprotein ethanol dehydrogenase; QHEDH; ADHIIB. Enzyme Commission Number: EC 1.1.9.1. 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-0438; alcohol dehydrogenase (azurin); EC 1.1.9.1; type II quinoprotein alcohol dehydrogenase; quinohaemoprotein ethanol dehydrogenase; QHEDH; ADHIIB. Cat No: EXWM-0438.
alcohol dehydrogenase (cytochrome c)
A periplasmic PQQ-containing quinoprotein. Occurs in Pseudomonas and Rhodopseudomonas. The enzyme from Pseudomonas aeruginosa uses a specific inducible cytochrome c550 as electron acceptor. Acts on a wide range of primary and secondary alcohols, but not methanol. It has a homodimeric structure [contrasting with the heterotetrameric structure of EC 1.1.2.7, methanol dehydrogenase (cytochrome c)]. It is routinely assayed with phenazine methosulfate as electron acceptor. Activity is stimulated by ammonia or amines. Like all other quinoprotein alcohol dehydrogenases it has an 8-bladed 'propeller' structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ. Group: Enzymes. Synonyms: type I quinoprotein alcohol dehydrogenase; quinoprotein ethanol dehydrogenase. Enzyme Commission Number: EC 1.1.2.8. 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-0390; alcohol dehydrogenase (cytochrome c); EC 1.1.2.8; type I quinoprotein alcohol dehydrogenase; quinoprotein ethanol dehydrogenase. Cat No: EXWM-0390.
alcohol dehydrogenase (quinone)
Only described in acetic acid bacteria where it is involved in acetic acid production. Associated with membrane. Electron acceptor is membrane ubiquinone. A model structure suggests that, like all other quinoprotein alcohol dehydrogenases, the catalytic subunit has an 8-bladed propeller structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ; the catalytic subunit also has a heme c in the C-terminal domain. The enzyme has two additional subunits, one of which contains three molecules of heme c. It does not require amines for activation. It has a restricted substrate specificity, oxidizing a few primary alcohols (C2 to C6), but not methanol, secondary alcohols and some aldehydes. It is assayed with phenazine methosulfate or with ferricyanide. Group: Enzymes. Synonyms: type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Enzyme Commission Number: EC 1.1.5.5. 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-0433; alcohol dehydrogenase (quinone); EC 1.1.5.5; type III ADH; membrane associated quinohaemoprotein alcohol dehydrogenase. Cat No: EXWM-0433.
aralkylamine dehydrogenase (azurin)
Phenazine methosulfate can act as acceptor. Acts on aromatic amines and, more slowly, on some long-chain aliphatic amines, but not on methylamine or ethylamine. Group: Enzymes. Synonyms: aromatic amine dehydrogenase; arylamine dehydrogenase; tyramine dehydrogenase; aralkylamine:(acceptor) oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.9.2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1489; aralkylamine dehydrogenase (azurin); EC 1.4.9.2; aromatic amine dehydrogenase; arylamine dehydrogenase; tyramine dehydrogenase; aralkylamine:(acceptor) oxidoreductase (deaminating). Cat No: EXWM-1489.
Azapentacene
Azapentacene is used in ophthalmologic eye lotions containing polymers with side-chains of phosphorylcholine analogs. Synonyms: 5,12-Dihydro-quinoxalino[2,3-b]phenazine sulfonate sodium salt; Sodium 5,12-dihydroazapentacene disulfonate; Phacolysine Sodium Salt ; Phacolin; Quinax. Grades: > 95%. CAS No. 3863-80-7. Molecular formula: C18H10N4O6S2Na2. Mole weight: 488.41.
Clofazimine
Antibacterial (tuberculostatic, leprostatic). Group: Biochemicals. Alternative Names: N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-[(1-methylethyl)imino]-2-phenazinamine; 3- (p-Chloroanilino) -10- (p-chlorophenyl) -2, 10-dihydro-2- (isopropylimino) phenazine; 2-(4-Chloroanilino)-3-isopropylimino-5-(4-chlorophenyl)-3,5-dihydrophenazine; B 663. Grades: Highly Purified. CAS No. 2030-63-9. Pack Sizes: 1g. US Biological Life Sciences.
Worldwide
CoB-CoM heterodisulfide reductase
This enzyme is found in methanogenic archaea, particularly Methanosarcina species, and regenerates coenzyme M and coenzyme B after the action of EC 2.8.4.1, coenzyme-B sulfoethylthiotransferase. Contains (per heterodimeric unit) two distinct b-type hemes and two [4Fe-4S] clusters. Highly specific for both coenzyme M and coenzyme B. Reacts with various phenazine derivatives, including 2-hydroxyphenazine and 2-bromophenazine. Group: Enzymes. Synonyms: heterodisulfide reductase; soluble heterodisulfide reductase. Enzyme Commission Number: EC 1.8.98.1. 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-1682; CoB-CoM heterodisulfide reductase; EC 1.8.98.1; heterodisulfide reductase; soluble heterodisulfide reductase. Cat No: EXWM-1682.
cytokinin dehydrogenase
A flavoprotein(FAD). Catalyses the oxidation of cytokinins, a family of N6-substituted adenine derivatives that are plant hormones, where the substituent is a dimethylallyl or other prenyl group. Although this activity was previously thought to be catalysed by a hydrogen-peroxide-forming oxidase, this enzyme does not require oxygen for activity and does not form hydrogen peroxide. 2,6-Dichloroindophenol, methylene blue, nitroblue tetrazolium, phenazine methosulfate and Cu(II) in the presence of imidazole can act as acceptors. This enzyme plays a part in regulating rice-grain production, with lower levels of the enzyme resulting in enhanced grain production. Group: Enzymes. Synonyms: N6-dimethylallyladenine:(acceptor) oxidoreductase; 6-N-dimethylallyladenine:acceptor oxidoreductase; OsCKX2; CKX; cytokinin oxidase/dehydrogenase. Enzyme Commission Number: EC 1.5.99.12. CAS No. 55326-39-1. 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-1566; cytokinin dehydrogenase; EC 1.5.99.12; 55326-39-1; N6-dimethylallyladenine:(acceptor) oxidoreductase; 6-N-dimethylallyladenine:acceptor oxidoreductase; OsCKX2; CKX; cytokinin oxidase/dehydrogenase. Cat No: EXWM-1566.
DC 86M
It is originally isolated from Streptomyces lugeogriseus 86. DC 86M has anti-Gram-positive bacteria and weak anti-Gram-negative bacteria activity, and can inhibit mouse sarcoma 180 cells. Synonyms: 6-(1-((Hydroxyacetyl)oxy)ethyl)-1-phenazinecarboxylic acid; DC-86-M; DC-86M; DC 86 M; 6-{1-[(Hydroxyacetyl)oxy]ethyl}phenazine-1-carboxylic acid. Grades: >98%. CAS No. 94448-15-4. Molecular formula: C17H14N2O5. Mole weight: 326.30.
DOB-41
DOB-41 is produced by the strain of Pseudomonas DOB-41. It has strong anti-gram-positive bacteria activity, and has the effect of inhibiting tumor. It prolongs the survival of transplanted leukemia P388 mice. Synonyms: Dob-41 antibiotic; Antibiotic dob 41; 6-[(R)-1-[(R)-3-Hydroxy-2-methoxy-1-oxopropoxy]ethyl]-1-phenazinecarboxylic acid. CAS No. 115666-98-3. Molecular formula: C19H18N2O6. Mole weight: 370.36.
formate dehydrogenase (cytochrome-c-553)
Yeast cytochrome c, ferricyanide and phenazine methosulfate can act as acceptor. Group: Enzymes. Enzyme Commission Number: EC 1.2.2.3. 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-1204; formate dehydrogenase (cytochrome-c-553); EC 1.2.2.3. Cat No: EXWM-1204.
glucose 1-dehydrogenase (PQQ, quinone)
Integral membrane protein containing PQQ as prosthetic group. It also contains bound ubiquinone and Mg2+ or Ca2+. Electron acceptor is membrane ubiquinone but usually assayed with phenazine methosulfate. Like in all other quinoprotein alcohol dehydrogenases the catalytic domain has an 8-bladed propeller structure. It occurs in a wide range of bacteria. Catalyses a direct oxidation of the pyranose form of D-glucose to the lactone and thence to D-gluconate in the periplasm. Oxidizes other monosaccharides including the pyranose forms of pentoses. Group: Enzymes. Synonyms: quinoprotein glucose dehydrogenase; membrane-bound glucose dehydrogenase; mGDH; glucose dehydrogenase (PQQ-dependent); glucose dehydrogenase (pyrroloquinoline-quinone); quinoprotein D-glucose dehydrogenase. Enzyme Commission Number: EC 1.1.5.2. CAS No. 81669-60-5. Glucose Dehyrogenase. 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-0430; glucose 1-dehydrogenase (PQQ, quinone); EC 1.1.5.2; 81669-60-5; quinoprotein glucose dehydrogenase; membrane-bound glucose dehydrogenase; mGDH; glucose dehydrogenase (PQQ-dependent); glucose dehydrogenase (pyrroloquinoline-quinone); quinoprotein D-glucose dehydrogenase. Cat No: EXWM-0430.
glycine dehydrogenase (cyanide-forming)
The enzyme from Pseudomonas sp. contains FAD. The enzyme is membrane-bound, and the 2-electron acceptor is a component of the respiratory chain. The enzyme can act with various artificial electron acceptors, including phenazine methosulfate. Group: Enzymes. Synonyms: hydrogen cyanide synthase; HCN synthase. Enzyme Commission Number: EC 1.4.99.5. 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-1491; glycine dehydrogenase (cyanide-forming); EC 1.4.99.5; hydrogen cyanide synthase; HCN synthase. Cat No: EXWM-1491.
glycolate dehydrogenase
Also acts on (R)-lactate. 2,6-Dichloroindophenol and phenazine methosulfate can act as acceptors. Group: Enzymes. Synonyms: glycolate oxidoreductase; glycolic acid dehydrogenase; glycolate:(acceptor) 2-oxidoreductase. Enzyme Commission Number: EC 1.1.99.14. CAS No. 37368-32-4. 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-0447; glycolate dehydrogenase; EC 1.1.99.14; 37368-32-4; glycolate oxidoreductase; glycolic acid dehydrogenase; glycolate:(acceptor) 2-oxidoreductase. Cat No: EXWM-0447.
Griseolutein A
It is produced by the strain of Streptomyces griseoluteus. Griseolutein A and Griseolutein B have similar activitiy against gram-positive and negative bacteria. Synonyms: 6-(((Hydroxyacetyl)oxy)methyl)-9-methoxy-1-phenazinecarboxylic acid; 1-Phenazinecarboxylic acid, 6-(hydroxymethyl)-9-methoxy-, glycolate (ester). Grades: >98%. CAS No. 573-84-2. Molecular formula: C17H14N2O6. Mole weight: 342.30.
Griseolutein B
It is produced by the strain of Streptomyces griseoluteus. Griseolutein A and Griseolutein B have similar activitiy against gram-positive and negative bacteria, and Griseolutein B also inhibits rickettsia, trichomonas vaginalis and Ehrlichite ascites cancer. Synonyms: 6-[(1,2-Dihydroxyethoxy)methyl]-9-methoxy-1-phenazinecarboxylic acid. Grades: >98%. CAS No. 2072-68-6. Molecular formula: C17H16N2O6. Mole weight: 344.32.
Hemipyocyanine
Hemipyocyanine, an α-Amylase inhibitor, is produced by the strain of Pseudomonas aeruginosa. It has anti-gram-positive bacteria, negative-bacteria, trichophyta, yeast and other fungi activities. Synonyms: 1-Hydroxyphenazine; 1-Phenazinol; Pyoxanthose; NSC 88882; Phenazine, 1-hydroxy-; 1-Hydroxy-5,10-diazaanthracene; 5H-phenazin-1-one; alpha-Hydroxyphenazine; 1-Hydroxy-9,10-diazaanthracene; Hemipyocyanin; Pyoxanthose; α-Hydroxyphenazine. Grades: >95%. CAS No. 528-71-2. Molecular formula: C12H8N2O. Mole weight: 196.21.
Homo fluorindine
Homo fluorindine. Group: Biochemicals. Alternative Names: 5,12-Dihydroquinoxalino[2,3-b]phenazine; 5,12-Dihydro-5,7,12,14-tetraazapentacene; 5,12-Dihydroquinoxalino[2,3-b]phenazine. Grades: Highly Purified. CAS No. 531-47-5. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C18H12N4. US Biological Life Sciences.
Worldwide
Iodinin
Iodinin is an antibiotic produced by the strain of Chromobacterium iodinum etc. It has antibacterial and fungal properties. Synonyms: 5,6-dihydroxy-10-oxidophenazin-10-ium-1-one; 1,6-Phenazinediol 5,10-dioxide. CAS No. 68-81-5. Molecular formula: C12H8N2O4. Mole weight: 244.20.
isoquinoline 1-oxidoreductase
The enzyme from Pseudomonas diminuta is specific towards N-containing N-heterocyclic substrates, including isoquinoline, isoquinolin-5-ol, phthalazine and quinazoline. Electron acceptors include 1,2-benzoquinone, cytochrome c, ferricyanide, iodonitrotetrazolium chloride, nitroblue tetrazolium, Meldola blue and phenazine methosulfate. Group: Enzymes. Enzyme Commission Number: EC 1.3.99.16. CAS No. 155948-73-5. 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-1421; isoquinoline 1-oxidoreductase; EC 1.3.99.16; 155948-73-5. Cat No: EXWM-1421.
Lomofungin
It is produced by the strain of Str. lomondensis var. lomondensis NRRL 3252. It is an antibiotic of the phenazine derivatives. It has anti-bacterial and fungal effects, but the anti-bacterial effects are weak. Synonyms: Lomondomycin; NSC 106995; NSC 156939; U-24792; 1-carbomethoxy-5-formyl-4,6,8-trihydroxyphenazine; 6-Formyl-4,7,9-trihydroxy-1-phenazinecarboxylic acid methyl ester. Grades: >95%. CAS No. 26786-84-5. Molecular formula: C15H10N2O6. Mole weight: 314.25.
L-sorbose 1-dehydrogenase
The product, L-sorbosone, is an intermediate in bacterial 2-keto-L-gulonic-acid formation. The activity of this membrane-bound enzyme is stimulated by Fe(III) or Co2+ but is inhibited by Cu2+. The enzyme is highly specific for L-sorboseas other sugars, such as glucose, mannitol and sorbitol, are not substrates. Phenazine methosulfate and DCIP can act as artificial acceptors. Group: Enzymes. Synonyms: SDH. Enzyme Commission Number: EC 1.1.99.32. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0461; L-sorbose 1-dehydrogenase; EC 1.1.99.32; SDH. Cat No: EXWM-0461.
methanol dehydrogenase (cytochrome c)
A periplasmic quinoprotein alcohol dehydrogenase that only occurs in methylotrophic bacteria. It uses the novel specific cytochrome cL as acceptor. Acts on a wide range of primary alcohols, including ethanol, duodecanol, chloroethanol, cinnamyl alcohol, and also formaldehyde. Activity is stimulated by ammonia or methylamine. It is usually assayed with phenazine methosulfate. Like all other quinoprotein alcohol dehydrogenases it has an 8-bladed 'propeller' structure, a calcium ion bound to the PQQ in the active site and an unusual disulfide ring structure in close proximity to the PQQ. It differs from EC 1.1.2.8, alcohol dehydrogenase (cytochrome c), in having a high affinity for methanol and in having a second essential small subunit (no known function). Group: Enzymes. Synonyms: methanol dehydrogenase; MDH. Enzyme Commission Number: EC 1.1.2.7. CAS No. 37205-43-9. 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-0389; methanol dehydrogenase (cytochrome c); EC 1.1.2.7; 37205-43-9; methanol dehydrogenase; MDH. Cat No: EXWM-0389.
Myxin
Myxin is a phenazine derivative produced by Sorangium sp. 3C. It has activity against gram-positive bacteria, negative bacteria, mycobacteria, yeasts and fungi. Synonyms: 6-Methoxy-1-phenazinol 5,10-dioxide. CAS No. 13925-12-7. Molecular formula: C13H10N2O4. Mole weight: 258.23.
Oxychloroaphine
It is produced by the strain of Pseudomonas aeruginosa T359. It's a phenazine antibiotic. It has antifungal and mycobacterium effects, and has weak inhibitory effect on gram-positive bacteria. Synonyms: Oxychloraphin; Oxychlororaphine; Oxychloroaphine; 1-Phenazinecarboxamide; 1-carbamoylphenazine. Grades: >98% by HPLC. CAS No. 550-89-0. Molecular formula: C13H9N3O. Mole weight: 223.23.
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