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| Product | Description | |
|---|---|---|
| Pseudomonic acid C | Pseudomonic acid C, an antibiotic, possesses antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 71980-98-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-133056. |  |
| Pseudomonic Acid C | Pseudomonic Acid C. Group: Biochemicals. Alternative Names: (2E)-5,9-Anhydro-2,3,4,8-tetradeoxy-8-(5-hydroxy-4-methyl-2-hexen-1-yl)-3-methyl-L-talo-Non-2-enonic Acid 8-Carboxyoctyl Ester; [2E,8(2E,4R,5S)]-5,9-Anhydro-2,3,4,8-tetradeoxy-8-(5-hydroxy-4-methyl-2-hexenyl)-3-methyl-L-talo-non-2-enonic Acid 8-Carboxyoctyl Ester; (+)-Pseudomonic acid C. Grades: Highly Purified. CAS No. 71980-98-8. Pack Sizes: 10mg. Molecular Formula: C26H44O8, Molecular Weight: 484.62. US Biological Life Sciences. |  Worldwide |
| Pseudomonic acid D sodium | Pseudomonic acid D sodium. Group: Biochemicals. Alternative Names: [1 (E) , 2E, 8[2S, 3S (1S, 2S) ]]-5, 9-Anhydro-2, 3, 4, 8-tetradeoxy-8-[[3- (2-hydroxy-1-methylpropyl) oxiranyl]methyl]-3-methyl-L-talo-non-2-enonic acid 8-carboxy-5-octenyl ester monosodium salt; Sodium pseudomonate D; Mupirocin Impurity C. Grades: Highly Purified. CAS No. 85178-60-5. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C26H41NaO9. US Biological Life Sciences. | Worldwide |
| Pseudomonic acid E | Pseudomonic acid E is an impurity of Mupirocin, which is a carboxylic acid bacteriostatic/bactericidal antibiotic. Synonyms: Mupirocin III; Mupirocin Impurity 2. CAS No. 167842-57-1. Molecular formula: C28H48O9. Mole weight: 528.67. |  |
| [1(Z), 2E, 8[2S, 3S(1S, 2S)]]- 5, 9-Anhydro-2, 3, 4, 8-tetradeoxy-8-[[3- (2-hydroxy-1-methylpropyl) oxiranyl]methyl]-3-methyl-L-talo-Non-2-enonic Acid 9-Methoxy-9-oxo-5-nonenyl Ester | [1(Z), 2E, 8[2S, 3S(1S, 2S)]]- 5, 9-Anhydro-2, 3, 4, 8-tetradeoxy-8-[[3- (2-hydroxy-1-methylpropyl) oxiranyl]methyl]-3-methyl-L-talo-Non-2-enonic Acid 9-Methoxy-9-oxo-5-nonenyl Ester is an intermediate in the synthesis of Pseudomonic Acid D Sodium (P839520) an antibiotic isolated from Pseudomonas fluorescens. Group: Biochemicals. Grades: Highly Purified. CAS No. 89254-47-7. Pack Sizes: 250ug, 500ug. Molecular Formula: C27H44O9. US Biological Life Sciences. | Worldwide |
| Mupirocin | Major component of the pseudomonic acid, an antibiotic complex produced by Pseudomonas fluorescens NCIB 10586. Topical antibacterial. Pseudomonic acid is a potent antibiotic produced by Pseudomonas fluorescens reported by Fuller et al. in 1971. Pseudomonic acid has broad spectrum activity against Gram positive bacteria and was approved for topical human use in 1985. Pseudomonic acid acts as a potent and selective inhibitor of isoleucyl-tRNA synthetase. Group: Biochemicals. Alternative Names: (2E)-5,9-Anhydro-2,3,4,8-tetradeoxy-8-[[(2S,3S)-3-[(1S,2S)-2-hydroxy-1-methylpropyl]-oxiranyl]methyl]-3-methyl-L-talo-non-2-enonic Acid 8-Carboxyoctyl Ester; BRL 4910A; Bactoderm; Bactroban; Bactroban Ointment; Mupirocin Neo-Sensitabs; Mupricin; Pseudomonic Acid; Pseudomonic Acid A; Turixin; trans-Pseudomonic Acid. Grades: Purified. CAS No. 12650-69-0. Pack Sizes: 500mg, 1g, 5g, 10g. Molecular Formula: C??H??O?, Molecular Weight: 500.62. US Biological Life Sciences. | Worldwide |
| Mupirocin | Mupirocin (BRL-4910A, Pseudomonic acid) is an orally active antibiotic isolated from Pseudomonas fluorescens. Mupirocin apparently exerts its antimicrobial activity by reversibly inhibiting isoleucyl-transfer RNA, thereby inhibiting bacterial protein and RNA synthesis [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: BRL-4910A; Pseudomonic acid. CAS No. 12650-69-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0958. | |
| Mupirocin | Mupirocin (BRL-4910A, Pseudomonic acid) is an orally active antibiotic isolated from Pseudomonas fluorescens. Mupirocin apparently exerts its antimicrobial activity by reversibly inhibiting isoleucyl-transfer RNA, thereby inhibiting bacterial protein and RNA synthesis. Uses: Designed for use in research and industrial production. Additional or Alternative Names: MUPIROCIN;MUPIROCIN CALCIUM;PSEUDOMONIC ACID;PSEUDOMONIC ACID A;(2s-(2-alpha(e;4-beta,5-alpha(2r*,3r*(1r*,2r*))))-3-beta;bactroban;nonanoicacid,9((3-methyl-1-oxo-4-(tetrahydro-3,4-dihydroxy-5-((3-(2-hydroxy-1. Product Category: Inhibitors. Appearance: solid. CAS No. 12650-69-0. Molecular formula: C26H44O9. Mole weight: 500.62. Purity: 0.99. IUPACName: 9-[(E)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[[(2S,3S)-3-[(2S,3S)-3-hydroxybutan-2-yl]oxiran-2-yl]methyl]oxan-2-yl]-3-methylbut-2-enoyl]oxynonanoicacid. Canonical SMILES: CC(C1C(O1)CC2COC(C(C2O)O)CC(=CC(=O)OCCCCCCCCC(=O)O)C)C(C)O. Density: 1.183 g/cm³. ECNumber: 603-145-3. Product ID: ACM12650690. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Mupirocin calcium hydrate | Mupirocin (BRL-4910A, Pseudomonic acid) calcium hydrate is an orally active antibiotic isolated from Pseudomonas fluorescens. Mupirocin calcium hydrate apparently exerts its antimicrobial activity by reversibly inhibiting isoleucyl-transfer RNA, thereby inhibiting bacterial protein and RNA synthesis [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: BRL-4910A calcium hydrate; Pseudomonic acid calcium hydrate. CAS No. 115074-43-6. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N7068. | |
| Mupirocin lithium | Mupirocin (BRL-4910A) lithium is an orally active antibiotic isolated from Pseudomonas fluorescens. Mupirocin lithium apparently exerts its antimicrobial activity by reversibly inhibiting isoleucyl-transfer RNA, thereby inhibiting bacterial protein and RNA synthesis [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BRL-4910A lithium; Pseudomonic acid lithium. CAS No. 73346-79-9. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-W108875. | |
| Mupirocin Lithium | It is a major component of the pseudomonic acid, an antibiotic complex produced by Pseudomonas fluorescens NCIB 10586. It is a carboxylic acid bacteriostatic/bactericidal antibiotic. Synonyms: L-talo-Non-2-enonic acid, 5,9-anhydro-2,3,4,8-tetradeoxy-8-[[(2S,3S)-3-[(1S,2S)-2-hydroxy-1-methylpropyl]oxiranyl]methyl]-3-methyl-, 8-carboxyoctyl ester, lithium salt, (2E)-; L-talo-Non-2-enonic acid, 5,9-anhydro-2,3,4,8-tetradeoxy-8-[[3-(2-hydroxy-1-methylpropyl)oxiranyl]methyl]-3-methyl-, 8-carboxyoctyl ester, monolithium salt, [2E,8[2S,3S(1S,2S)]]-; Lithium mupirocin; Lithium pseudomonate; Li-MUP. Grades: ≥95.0%. CAS No. 73346-79-9. Molecular formula: C26H43LiO9. Mole weight: 506.56. | |
| 10-Undecenoic acid,98% (stabilized with TBC) | 10-Undecenoic acid (Undecylenic acid) is an antifungal agent. 10-Undecenoic acid inhibits Aβ oligomerization, scavenges ROS and inhibits μ-calpain activity. 10-Undecenoic acid has neuroprotective effects. 10-Undecenoic acid has anticancer effects on a variety of tumors. 10-Undecenoic acid inhibits C. albicans biofilm formation and MRSA infection. 10-Undecenoic acid inhibits quorum sensing signals of Bacillus subtilis and Pseudomonas aeruginosa [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Natural products. Alternative Names: Undecylenic acid. CAS No. 112-38-9. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-B0914. | |
| 10-Undecenoic acid (Standard) | 10-Undecenoic acid (Standard) is the analytical standard of 10-Undecenoic acid. This product is intended for research and analytical applications. 10-Undecenoic acid (Undecylenic acid) is an antifungal agent. 10-Undecenoic acid inhibits Aβ oligomerization, scavenges ROS and inhibits μ-calpain activity. 10-Undecenoic acid has neuroprotective effects. 10-Undecenoic acid has anticancer effects on a variety of tumors. 10-Undecenoic acid inhibits C. albicans biofilm formation and MRSA infection. 10-Undecenoic acid inhibits quorum sensing signals of Bacillus subtilis and Pseudomonas aeruginosa [1] [2] [3] [4] [5] [6] [7] [8]. Uses: Scientific research. Group: Natural products. CAS No. 112-38-9. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-B0914R. | |
| 1,3,7-trimethyluric acid 5-monooxygenase | The enzyme, characterized from the bacterium Pseudomonas sp. CBB1, is part of the bacterial C-8 oxidation-based caffeine degradation pathway. The product decomposes spontaneously to a racemic mixture of 3,6,8-trimethylallantoin. The enzyme shows no acitivity with urate. cf. EC 1.14.13.113, FAD-dependent urate hydroxylase. Group: Enzymes. Synonyms: tmuM (gene name). Enzyme Commission Number: EC 1.14.13.212. 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-0814; 1,3,7-trimethyluric acid 5-monooxygenase; EC 1.14.13.212; tmuM (gene name). Cat No: EXWM-0814. |  |
| 1-Ethyl-1,4-dihydro-4-oxo-7-(4-pyridyl)quinoline-3-carboxylic Acid Ethyl Ester | 1-Ethyl-1,4-dihydro-4-oxo-7-(4-pyridyl)quinoline-3-carboxylic Acid Ethyl Ester is an intermediate in the synthesis of Rosoxacin (R693580), an antibacterial agent used against Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pneumoniae. Group: Biochemicals. Grades: Highly Purified. CAS No. 40034-46-6. Pack Sizes: 5mg, 10mg. Molecular Formula: C19H18N2O3. US Biological Life Sciences. | Worldwide |
| (2,2,3-trimethyl-5-oxocyclopent-3-enyl)acetyl-CoA 1,5-monooxygenase | A FAD dependent enzyme isolated from Pseudomonas putida. Forms part of the catabolism pathway of camphor. It acts on the CoA ester in preference to the free acid. Group: Enzymes. Synonyms: 2-oxo-Δ3-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase; 2-oxo-Δ3-4,5,5-trimethylcyclopentenylacetyl-CoA 1,2-monooxygenase; OTEMO. Enzyme Commission Number: EC 1.14.13.160. 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-0760; (2,2,3-trimethyl-5-oxocyclopent-3-enyl)acetyl-CoA 1,5-monooxygenase; EC 1.14.13.160; 2-oxo-Δ3-4,5,5-trimethylcyclopentenylacetyl-CoA monooxygenase; 2-oxo-Δ3-4,5,5-trimethylcyclopentenylacetyl-CoA 1,2-monooxygenase; OTEMO. Cat No: EXWM-0760. | |
| 2- [ [ (3-Bromophenyl) amino] methylene] propanedioic Acid 1,3-Diethyl Ester | 2- [ [ (3-Bromophenyl) amino] methylene] propanedioic Acid 1,3-Diethyl Ester is an intermediate in the synthesis of Rosoxacin (R693580), an antibacterial agent used against Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphylococcus aureus and Streptococcus pneumoniae. Group: Biochemicals. Grades: Highly Purified. CAS No. 351893-47-5. Pack Sizes: 50mg, 100mg. Molecular Formula: C14H16BrNO4, Molecular Weight: 342.19. US Biological Life Sciences. | Worldwide |
| 2,4-Bis(benzyloxy)-6-propylbenzaldehyde | 2,4-Bis(benzyloxy)-6-propylbenzaldehyde is an intermediate in synthesizing Divarinic Acid (D494463), an antibacterial compound that strongly inhibits bacterial growth of Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg, 250mg. Molecular Formula: C24H24O3. US Biological Life Sciences. | Worldwide |
| 2,4-Bis(phenylmethoxy)-6-propylbenzoic Acid | 2,4-Bis(phenylmethoxy)-6-propylbenzoic Acid is an intermediate in synthesizing Divarinic Acid (D494463), an antibacterial compound that strongly inhibits bacterial growth of Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa. Group: Biochemicals. Grades: Highly Purified. CAS No. 104847-69-0. Pack Sizes: 50mg, 100mg. Molecular Formula: C24H24O4. US Biological Life Sciences. | Worldwide |
| 2,4-Dihydroxy-6-propylbenzaldehyde | 2,4-Dihydroxy-6-propylbenzaldehyde possesses strong anti-septic action; Also, it is an intermediate used in the synthesis of Divarinic Acid (D494463), which is an antibacterial compound that strongly inhibits bacterial growth of Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa. Group: Biochemicals. Grades: Highly Purified. CAS No. 37455-87-1. Pack Sizes: 100mg, 250mg. Molecular Formula: C10H12O3, Molecular Weight: 180.2. US Biological Life Sciences. | Worldwide |
| 2-Acetamido-2-deoxy-D-galacturonic Acid | A component of O-antigens of Pseudomonas aeruginosa. Uses: A component of o-antigens of pseudomonas aeruginosa. Synonyms: 2-(Acetylamino)-2-deoxy-D-galacturonic Acid. CAS No. 45171-33-3. Molecular formula: C8H13NO7. Mole weight: 235.19. | |
| 2-(acetamidomethylene)succinate hydrolase | Involved in the degradation of pyridoxin in Pseudomonas. Group: Enzymes. Synonyms: α-(N-acetylaminomethylene)succinic acid hydrolase. Enzyme Commission Number: EC 3.5.1.29. CAS No. 37289-09-1. 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-4418; 2-(acetamidomethylene)succinate hydrolase; EC 3.5.1.29; 37289-09-1; α-(N-acetylaminomethylene)succinic acid hydrolase. Cat No: EXWM-4418. | |
| 2-aminomuconate deaminase | 2-Aminomuconate is an intermediate in the bacterial biodegradation of nitrobenzene. The enzyme has been isolated from several species, including Pseudomonas pseudocaligenes JS45, Pseudomonas fluorescens KU-7, Pseudomonas sp. AP3 and Burkholderia cenocepacia J2315. The reaction is spontaneous in acid conditions. Group: Enzymes. Synonyms: amnD (gene name); nbaF (gene name). Enzyme Commission Number: EC 3.5.99.5. CAS No. 201098-29-5. 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-4588; 2-aminomuconate deaminase; EC 3.5.99.5; 201098-29-5; amnD (gene name); nbaF (gene name). Cat No: EXWM-4588. | |
| 2-Carboxybenzaldehyde | 2-Carboxybenzaldehyde is the major metabolite found in phenanthrene metabolism. Phenanthrene can be degrade by Pseudomonas sp. Lphe-2 strain [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Phthalaldehydic acid. CAS No. 119-67-5. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g. Product ID: HY-Y1771. | |
| 2-dehydro-3-deoxy-D-gluconate 5-dehydrogenase | The enzyme from Pseudomonas acts equally well on NAD+ or NADP+, while that from Erwinia chrysanthemi and Escherichia coli is more specific for NAD+. Group: Enzymes. Synonyms: 2-keto-3-deoxygluconate 5-dehydrogenase; 2-keto-3-deoxy-D-gluconate dehydrogenase; 2-keto-3-deoxygluconate (nicotinamide adenine dinucleotide (phosphate)) dehydrogenase; 2-keto-3-deoxy-D-gluconate (3-deoxy-D-glycero-2,5-hexodiulosonic acid) dehydrogenase. Enzyme Commission Number: EC 1.1.1.127. CAS No. 37250-56-9. 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-0031; 2-dehydro-3-deoxy-D-gluconate 5-dehydrogenase; EC 1.1.1.127; 37250-56-9; 2-keto-3-deoxygluconate 5-dehydrogenase; 2-keto-3-deoxy-D-gluconate dehydrogenase; 2-keto-3-deoxygluconate (nicotinamide adenine dinucleotide (phosphate)) dehydrogenase; 2-keto-3-deoxy-D-gluconate (3-deoxy-D-glycero-2,5-hexodiulosonic acid) dehydrogenase. Cat No: EXWM-0031. | |
| 2-haloacid dehalogenase (configuration-inverting) | Dehalogenates both (S)- and (R)-2-haloalkanoic acids to the corresponding (R)- and (S)-hydroxyalkanoic acids, respectively, with inversion of configuration at C-2. The enzyme from Pseudomonas sp. 113 acts on 2-haloalkanoic acids whose carbon chain lengths are five or less. [See also EC 3.8.1.2 (S)-2-haloacid dehalogenase, EC 3.8.1.9 (R)-2-haloacid dehalogenase and EC 3.8.1.11 2-haloacid dehalogenase (configuration-retaining)]. Group: Enzymes. Synonyms: 2-haloalkanoic acid dehalogenase; 2-haloalkanoid acid halidohydrolase; DL-2-haloacid dehalogenase; DL-2-haloacid dehalogenase (inversion of configuration); DL-2-haloacid halidohydrolase (inversion of configuration); DL-DEXi; (R,S)-2-haloacid dehalogenase (configuration-inverting). Enzyme Commission Number: EC 3.8.1.10. 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-4740; 2-haloacid dehalogenase (configuration-inverting); EC 3.8.1.10; 2-haloalkanoic acid dehalogenase; 2-haloalkanoid acid halidohydrolase; DL-2-haloacid dehalogenase; DL-2-haloacid dehalogenase (inversion of configuration); DL-2-haloacid halidohydrolase (inversion of configuration); DL-DEXi; (R,S)-2-haloacid dehalogenase (configuration-inverting). Cat No: EXWM-4740. | |
| 2-Hydroxydecanoic Acid | 2-Hydroxydecanoic Acid is used in the study of drug absorption by intestinal mucosal enhancement using decanoic acid and its derivatives. In the production of quorum sensing inhibitors in growing onion bulbs infected with Pseudomonas aeruginosa E (HQ324110). Studies on part of carboxylic acid found in human blood. Group: Biochemicals. Grades: Highly Purified. CAS No. 5393-81-7. Pack Sizes: 50mg, 100mg. Molecular Formula: C10H20O3, Molecular Weight: 188.26. US Biological Life Sciences. | Worldwide |
| 2-(hydroxymethyl)-3-(acetamidomethylene)succinate hydrolase | Involved in the degradation of pyridoxin by Pseudomonas and Arthrobacter. Group: Enzymes. Synonyms: compound B hydrolase; α-hydroxymethyl-α'-(N-acetylaminomethylene)succinic acid hydrolase. Enzyme Commission Number: EC 3.5.1.66. CAS No. 95829-26-8. 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-4456; 2-(hydroxymethyl)-3-(acetamidomethylene)succinate hydrolase; EC 3.5.1.66; 95829-26-8; compound B hydrolase; α-hydroxymethyl-α'-(N-acetylaminomethylene)succinic acid hydrolase. Cat No: EXWM-4456. | |
| 2-ketoarginine methyltransferase | The enzyme is involved in production of the rare amino acid 3-methylarginine, which is used by the epiphytic bacterium Pseudomonas syringae pv. syringae as an antibiotic against the related pathogenic species Pseudomonas syringae pv. glycinea. Group: Enzymes. Synonyms: mrsA (gene name). Enzyme Commission Number: EC 2.1.1.243. 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-1846; 2-ketoarginine methyltransferase; EC 2.1.1.243; mrsA (gene name). Cat No: EXWM-1846. | |
| 3-Aminobenzoic-d4 Acid | A chemoattractants against Pseudomonas strains. A reactant used in the preparation of influenza neuraminidase inhibitors, inhibitors of transthyretin amyloid fibril formation and Iihibitors of the protein chaperone Hsp90. Group: Biochemicals. Alternative Names: 3-Aminobenzenecarboxylic Acid; 3-Carboxyaniline; Aniline-3-carboxylic Acid; NSC 15012; m-Aminobenzoic Acid; m-Anthranilic Acid; m-Carboxyaniline; m-Carboxyphenylamine. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 3-Hydroxyoctanoic acid | 3-Hydroxyoctanoic acid is a hydroxylated fatty acid that has been found in the LPS of Pseudomonas aeruginosa and in methyl-branched poly(3-hydroxyalkanoate) (PHA) polymers produced by Pseudomonas oleophores. It is an agonist of the orphan receptor GPR109B, increasing intracellular calcium in human neutrophils endogenously expressing GPR109B. 3-Hydroxycaprylic acid prevents lipolysis in human adipocytes and is upregulated in human plasma in response to a ketogenic diet. Plasma levels of 3-hydroxyoctanoic acid were also increased 3.41-fold in human male runners exhausted on a treadmill and in a mouse model of autism spectrum disorder (ASD) fed a high-glycemic diet. Uses: Scientific research. Group: Natural products. CAS No. 14292-27-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-113058. | |
| 4-Aminosalicylic acid | 4-Aminosalicylic acid. Uses: 4-aminosalicylic acid (4-asa) can be used in the synthesis of: azo derivatives of 4-asa with anti-inflammatory effects. ammonium 4-aminosalicylate salt polymorphs which are used as pharmaceutical ingredients. salicylic acid-triazole analogs which are used as quorum sensing inhibitors against pseudomonas aeruginosa. Additional or Alternative Names: 4-Amino-2-hydroxybenzoic acid, PAS. Product Category: Amino Acids. CAS No. 65-49-6. Molecular formula: H2NC6H3-2-(OH)CO2H. Mole weight: 153.14. Canonical SMILES: Nc1ccc(C(O)=O)c(O)c1. ECNumber: 200-613-5. Product ID: ACM65496-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| 4-Chlorophenylacetic acid | 4-Chlorophenylacetic acid is a compound belongs to a family of small aromatic fatty acids with anticancer properties. 4-Chlorophenylacetic acid can provide carbon and energy for Pseudomonas sp [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1878-66-6. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g; 100 g. Product ID: HY-W010062. | |
| 4-hydroxybenzoate 3-monooxygenase | A flavoprotein (FAD). Most enzymes from Pseudomonas are highly specific for NADPH (cf. EC 1.14.13.33 4-hydroxybenzoate 3-monooxygenase [NAD(P)H]). Group: Enzymes. Synonyms: p-hydroxybenzoate hydrolyase; p-hydroxybenzoate hydroxylase; 4-hydroxybenzoate 3-hydroxylase; 4-hydroxybenzoate monooxygenase; 4-hydroxybenzoic hydroxylase; p-hydroxybenzoate-3-hydroxylase; p-hydroxybenzoic acid hydrolase; p-hydroxybenzoic acid hydroxylase; p-hydroxybenzoic hydroxylase. Enzyme Commission Number: EC 1.14.13.2. CAS No. 9059-23-8. p-Hydroxybenzoate Hydroxylase. 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-0800; 4-hydroxybenzoate 3-monooxygenase; EC 1.14.13.2; 9059-23-8; p-hydroxybenzoate hydrolyase; p-hydroxybenzoate hydroxylase; 4-hydroxybenzoate 3-hydroxylase; 4-hydroxybenzoate monooxygenase; 4-hydroxybenzoic hydroxylase; p-hydroxybenzoate-3-hydroxylase; p-hydroxybenzoic acid hydrolase; p-hydroxybenzoic acid hydroxylase; p-hydroxybenzoic hydroxylase. Cat No: EXWM-0800. | |
| 4-hydroxyphenylpyruvate dioxygenase | The Pseudomonas enzyme contains one Fe3+ per mole of enzyme; the enzymes from other sources may contain essential iron or copper. Group: Enzymes. Synonyms: p-hydroxyphenylpyruvic hydroxylase; p-hydroxyphenylpyruvate hydroxylase; p-hydroxyphenylpyruvate oxidase; p-hydroxyphenylpyruvic oxidase; p-hydroxyphenylpyruvate dioxygenase; p-hydroxyphenylpyruvic acid hydroxylase; 4-hydroxyphenylpyruvic acid dioxygenase. Enzyme Commission Number: EC 1.13.11.27. CAS No. 9029-72-5. 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-0546; 4-hydroxyphenylpyruvate dioxygenase; EC 1.13.11.27; 9029-72-5; p-hydroxyphenylpyruvic hydroxylase; p-hydroxyphenylpyruvate hydroxylase; p-hydroxyphenylpyruvate oxidase; p-hydroxyphenylpyruvic oxidase; p-hydroxyphenylpyruvate dioxygenase; p-hydroxyphenylpyruvic acid hydroxylase; 4-hydroxyphenylpyruvic acid dioxygenase. Cat No: EXWM-0546. | |
| 4-O-Methylsuperolivetoric acid | 4-O-Methylsuperolivetoric acid is a metabolite of lichen obtained from Pseudomonas crassicarpa. CAS No. 108544-39-4. Molecular formula: C31H42O8. Mole weight: 542.66. | |
| 7-Bromoacetyl aminocephalosporanic Acid | An analog of glutaryl-7-amino cephalosporanic acid (GL-7-ACA). Can inhibit and specifically alkylate GL-7-ACA acylase (C130) from Pseudomonas sp.130 by forming a carbon-carbon bond between BA-7-ACA and the C-2 on indole ring of Trp- β4 residue of C130. Group: Biochemicals. Alternative Names: (6R-trans)-3-[(Acetyloxy)methyl]-7-[(bromoacetyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; 7- (2-Bromoacetamido) cephalosporanic Acid. Grades: Highly Purified. CAS No. 26973-80-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| ACYL-COENZYME A SYNTHETASE | ACYL-COENZYME A SYNTHETASE. Synonyms: EC 6.2.1.3;ACID: COA LIGASE (AMP-FORMING);ACYL-COENZYME A SYNTHETASE;Synthetase, acyl coenzyme A;ACYL-COENZYME A SYNTHETASE FROM PSEUDO-M ONAS SP., ~2.5U/MG;acyl-coenzyme a synthetase from pseudomonas sp.;Acyl-coenzyme A Synthetase [>=8 units/mg];Acyl-CoA Synthetase. CAS No. 9013-18-7. Pack Sizes: 1 kg. Product ID: CDF4-0057. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; ACYL-COENZYME A SYNTHETASE; CDF4-0057; 9013-18-7; 232-747-5; 9013-18-7. Purity: 0.99. Color: White. EC Number: 232-747-5. Physical State: Powder. Storage: -20°C. Product Description: Acyl-coenzyme A synthetase belongs to adenylate-forming enzymes superfamily. It has a conserved adenosine triphosphate/adenosine monophosphate (ATP/AMP) binding motif. |  |
| Alanylbactobolin | It is produced by the strain of Pseudomonas sp. BMG 13-A7. It has anti-gram-positive bacteria, negative bacteria and tumor activity. Synonyms: Bactobolin B; L-Alaninamide, L-alanyl-N-(3-(dichloromethyl)-3,4,4a,5,6,7-hexahydro-5,6,8-trihydroxy-3-methyl-1-oxo-1H-2-benzopyran-4-yl)-, (3S-(3-alpha,4-alpha,4a-beta,5-beta,6-alpha))-; DTXSID80995581; 5-Amino-2-{[3-(dichloromethyl)-1,5,6-trihydroxy-3-methyl-8-oxo-4,4a,5,6,7,8-hexahydro-3H-2-benzopyran-4-yl]amino}-4-oxohexanimidic acid. CAS No. 74141-68-7. Molecular formula: C17H25N3O7Cl2. Mole weight: 454.30. | |
| allophanate hydrolase | Along with EC 3.5.2.15 (cyanuric acid amidohydrolase) and EC 3.5.1.84 (biuret amidohydrolase), this enzyme forms part of thecyanuric-acid metabolism pathway, which degrades s-triazide herbicides, such as atrazine [2-chloro-4-(ethylamino)-6-(isopropylamino)-1,3,5-triazine], in bacteria. The yeast enzyme (but not that from green algae) also catalyses the reaction of EC 6.3.4.6, urea carboxylase, thus bringing about the hydrolysis of urea to CO2 and NH3 in the presence of ATP and bicarbonate. The enzyme from Pseudomonas sp. strain ADP has a narrow substrate specificity, being unable to use the structurally analogous compounds urea, hydroxyurea or methylcarbamate as substrate. Group: Enzymes. Synonyms: allophanate lyase; AtzF; TrzF. Enzyme Commission Number: EC 3.5.1.54. CAS No. 9076-72-6. 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-4443; allophanate hydrolase; EC 3.5.1.54; 9076-72-6; allophanate lyase; AtzF; TrzF. Cat No: EXWM-4443. | |
| AMIKACIN SULFATE | Amikacin disulfate is an aminoglycoside sulfate salt obtained by combining amikacin with two molar equivalents of sulfuric acid. It has a role as an antibacterial drug, an antimicrobial agent and a nephrotoxin. It contains an amikacin(4+). CAS No. 39831-55-5. Product ID: PAP-0040. Molecular formula: C22H45N5O17S. Category: Antibacterial, anti-inflammatory and antiviral. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; AMIKACIN SULFATE; PAP-0040; Antibacterial, anti-inflammatory and antiviral; C22H45N5O17S; 39831-55-5. Standard: EP/ USP/ CP. Color: white to off-white. EC Number: 254-648-6. Physical State: solid. Solubility: H2O: soluble50mg/mL. Storage: Inert atmosphere,2-8°C. Applications: Amikacin sulfate is a semi-synthetic aminoglycoside antibiotic, the antibacterial spectrum is similar to gentamicin, and it is effective against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and Proteus. Product Description: Amikacin sulfate is a semi-synthetic aminoglycoside antibiotic, the antibacterial spectrum is similar to gentamicin, and it is effective against Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli and Proteus. | |
| arogenate dehydrogenase [NAD(P)+] | Arogenate dehydrogenases may utilize NAD+ (EC 1.3.1.43), NADP+ (EC 1.3.1.78), or both (EC 1.3.1.79). Enzymes that can utilize both cofactors have been reported from some Proteobacteria, including Burkholderia caryophylli, Burkholderia cepacia, Pseudomonas marginata and Delftia acidovorans. Group: Enzymes. Synonyms: arogenic dehydrogenase (ambiguous); cyclohexadienyl dehydrogenase; pretyrosine dehydrogenase (ambiguous). Enzyme Commission Number: EC 1.3.1.79. CAS No. 64295-75-6. 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-1348; arogenate dehydrogenase [NAD(P)+]; EC 1.3.1.79; 64295-75-6; arogenic dehydrogenase (ambiguous); cyclohexadienyl dehydrogenase; pretyrosine dehydrogenase (ambiguous). Cat No: EXWM-1348. | |
| Aspoxicillin | Aspoxicillin is a semi-synthetic penicillin prepared from 6-aminopenicillanic acid (6-APA) or Amoxicillin. It has a broad antibacterial spectrum and has an effect on Pseudomonas aeruginosa. Synonyms: Aspoxicilina; Aspoxicilline; Aspoxicillinum. Grades: >98%. CAS No. 63358-49-6. Molecular formula: C21H27N5O7S. Mole weight: 493.53. | |
| Bacterial alginate - from fermentation of Azotobacter vinelandii or Pseudomonas mendocina | Bacterial alginate is an alginate produced by the fermentation of Azotobacter vinelandii or Pseudomonas mendocina. The structure consists of blocks of polymannuronic acid (poly M), polyguluronic acid (poly G) and alternating blocks of the two uronic acids (poly MG). Mole weight: ~100KDa. | |
| β-ketodecanoyl-[acyl-carrier-protein] synthase | This enzyme, which has been characterized from the bacterium Pseudomonas aeruginosa PAO1, catalyses the condensation of octanoyl-CoA, obtained from exogenously supplied fatty acids via β-oxidation, with malonyl-[acp], forming 3-oxodecanoyl-[acp], an intermediate of the fatty acid elongation cycle. The enzyme provides a shunt for β-oxidation degradation intermediates into de novo fatty acid biosynthesis. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.207. 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-2152; β-ketodecanoyl-[acyl-carrier-protein] synthase; EC 2.3.1.207. Cat No: EXWM-2152. | |
| BLP-1654 | BLP-1654 is a semi-synthetic penicillin made from 6-aminopenicillanic acid (6-APA). It has anti-Gram-positive and negative bacteria activity, especially for Pseudomonas bacteria. Synonyms: 6- (D-alpha- (3-Guanylureido) phenylacetamido) penicillanic acid. Grades: >98%. CAS No. 28889-87-4. Molecular formula: C18H22N6O5S. Mole weight: 434.47. | |
| Bongkrekic acid | Bongkrekic acid is a mitochondrial toxin secreted by the bacteria Pseudomonas cocovenenans [1]. Bongkrekic acid specific ligand for mitochondrial adenine nucleotide translocase (ANT) rather than the electron transport chain. Bongkrekic acid has to cross the mitochondrial inner membrane to produce its inhibitory effect on ADP/ATP transport [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 11076-19-0. Pack Sizes: 100 μg (2.06 mM in 100 μL Tris); 500 μg (2.06 mM in 500 μL Tris). Product ID: HY-136406. | |
| Bongkrekic acid | Bongkrekic acid is an acid-labile toxin produced by Pseudomonas cocoveneans. Uses: Anti-bacterial agents. Synonyms: (2E,4Z,6R,8Z,10E,14E,17S,18E,20Z)-20-(Carboxymethyl)-6-methoxy-2,5,17-trimethyl-2,4,8,10,14,18,20-docosaheptaenedioic Acid; (-)-Bongkrekic Acid; BA; Flavotoxin A. Grades: ≥98%. CAS No. 11076-19-0. Molecular formula: C28H38O7. Mole weight: 486.60. | |
| Bongkrekic acid solution | from Pseudomonas cocovenenans, ?95% (HPLC), ~1 mg/mL. Group: Fluorescence/luminescence spectroscopy. |  |
| Bulgecin A | Bulgecin A is an amino sugar produced by Pseudomonas acidophila G63O2 and P. mewacidophila SB 72310. It has Bulge-inducing activity, which can enhance the lysis of lactam antibiotics. Synonyms: BLG; BUL; 4-O-(4-O-SULFONYL-N-ACETYLGLUCOSAMININYL)-5-METHYLHYDROXY-L-PROLINE-TAURINE. CAS No. 92953-54-3. Molecular formula: C16H29N3O14S2. Mole weight: 551.54. | |
| Bulgecin B | Bulgecin B is an amino sugar produced by Pseudomonas acidophila G63O2 and P. mewacidophila SB 72310. It has Bulge-inducing activity, which can enhance the lysis of lactam antibiotics. Molecular formula: C17H29N3O13S. Mole weight: 515.49. | |
| Bulgecin C | Bulgecin C is an amino sugar produced by Pseudomonas acidophila G63O2 and P. mewacidophila SB 72310. It has Bulge-inducing activity, which can enhance the lysis of lactam antibiotics. Synonyms: 4-({2-Deoxy-2-[(1-hydroxyethylidene)amino]-4-O-sulfohexopyranosyl}oxy)-5-(hydroxymethyl)proline; L-Proline, 4-((2-(acetylamino)-2-deoxy-4-O-sulfo-beta-D-glucopyranosyl)oxy)-5-(hydroxymethyl)-, (2alpha,4alpha,5beta)-. CAS No. 92953-56-5. Molecular formula: C14H24N2O12S. Mole weight: 444.41. | |
| Carbenicillin | It is produced by the strain of Semisynthetic penicillin, 6-APA. Carbenicillin is a broad-spectrum semisynthetic penicillin derivative used parenterally. It is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity. It is used to treat pseudomonas aeruginosa infection. Synonyms: Carboxybenzylpenicillin; alpha-Carboxybenzylpencillin; Carbenicilina; Carbenicilline; Carbenicillinum; Pyopen; Carboxybenzylpenicillin acid; CBPC; Geopen. Grades: >98%. CAS No. 4697-36-3. Molecular formula: C17H18N2O6S. Mole weight: 378.40. | |
| Carumonam | It is produced by the strain of Monobactams. As well as Azthreonam, it has excellent curative effect on aerobic gram-negative bacteria (including Pseudomonas aeruginosa) infection, but no effect on gram-positive bacteria and anaerobic bacteria. Synonyms: Carumonamum; AMA 1080; (Z)-Carumonam; 2-[(Z)-[1-(2-amino-1,3-thiazol-4-yl)-2-[[(2S,3S)-2-(carbamoyloxymethyl)-4-oxo-1-sulfoazetidin-3-yl]amino]-2-oxoethylidene]amino]oxyacetic acid; CRMN; CARUMONAM. Grades: 95%. CAS No. 87638-04-8. Molecular formula: C12H14N6O10S2. Mole weight: 466.40. | |
| Cefamandole | It is produced by the strain of Semisynthetic second generation cephalosporin for injection. The activity of gram-positive bacteria was similar to cefthiophene, and it is sensitive to gram-negative bacteria including Escherichia coli, Pneumococci, Proteus, influenzae, typhoid, dysentery and enterobacter, but has no effect on pseudomonas aeruginosa and Serratia. All anaerobic bacteria were sensitive except the fragile bacilli and Clostridium difficile. Uses: A broad-spectrum cephalosporin antibiotic. Synonyms: (6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic acid; Cefadole; Cephadole; CEPHAMANDOLE; Cefamandol; Cefamandolum; L-Cefamandole. Grades: ≥98%. CAS No. 34444-01-4. Molecular formula: C18H18N6O5S2. Mole weight: 462.50. | |
| Cefathiamidine Impurity 1 | An analog of glutaryl-7-amino cephalosporanic acid (GL-7-ACA). Can inhibit and specifically alkylate GL-7-ACA acylase (C130) from Pseudomonas sp.130 by forming a carbon-carbon bond between BA-7-ACA and the C-2 on indole ring of Trp-β4 residue of C130. Synonyms: (6R-trans)-3-[(Acetyloxy)methyl]-7-[(bromoacetyl)amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; 7-(2-Bromoacetamido)cephalosporanic Acid. Grades: > 95%. CAS No. 26973-80-8. Molecular formula: C12H13BrN2O6S. Mole weight: 393.22. | |
| Cefoperazone | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Cefoperazone with the third generation of cephalosporin connectivity, and has good antibacterial effect to pseudomonas aeruginosa (MIC90 is 8 ?/mL). It is also used in the treatment of Pseudomonas infections. It has been used to treat respiratory tract infections, peritonitis, skin infections, endometritis, and bacterial septicemia. Uses: Anti-bacterial agents. Synonyms: Cefobid; Cefoperazono; Cefoperazonum; Medocef; Cefob; WAY-362450; FXR-450; WAY 362450; FXR 450; WAY362450; FXR450; T1551; T-1551; T 1551; C06883; C-06883; C 06883; D07645; D-07645; D 07645; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2R)-[[(4-ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino](4-hydroxyphenyl)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R,7R)-. Grades: ≥98%. CAS No. 62893-19-0. Molecular formula: C25H27N9O8S2. Mole weight: 645.67. | |
| Cefoperazone, Sodium Salt (CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid) | Cefoperazone is a third generation cephalosporin antibiotic. Cefoperazone exerts its bactericidal effect by inhibiting the bacterial cell wall synthesis, and sulbactam acts as a beta-lactamase inhibitor, to increase the antibacterial activity of cefoperazone against beta-lactamase producing organisms. It is one of few cephalosporin antibiotics effective in treating Pseudomonas bacterial infections which are otherwise resistant to these antibiotics. Group: Biochemicals. Alternative Names: CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid; (6R, 7R) -7-[[ (2R) -2-[[ (4-Ethyl-2, 3-dioxo-1-piperazinyl) carbonyl]amino]-2- (4-hydroxyphenyl) acetyl]amino]-3-[[ (1-methyl-1H-tetrazol-5-yl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Sodium Salt. Grades: Highly Purified. CAS No. 62893-20-3. Pack Sizes: 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Cefoselis sulfate | Cefoselis sulfate is a stable cephalosporin for BETA-lactamase. The drug shows antimicrobial activity for a wide range of bacteria including Pseudomonas. Synonyms: Winsef; (6R- (6alpha, 7beta (Z)))-7- ( ( (2-Amino-4-thiazolyl) (methoxyimino)acetyl)amino)-3- ( (2, 3-dihydro-2- (2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl)methyl)-8-oxo-5-Thia-1-azabicyclo (4. 2. 0)oct-2-ene-2-carboxylic acid sulfate. Grades: 0.98. CAS No. 122841-12-7. Molecular formula: C19H22N8O6S2.H2SO4. Mole weight: 620.64. | |
| Chemically modified Pseudomonas species Cholesterol Esterase | Hydrolase that splits fatty acids from sterols. Take advantage of the enhanced stability of this enzyme in liquid reagents. Rely on the proven diagnostic quality of this product. Applications: Use cholesterol esterase, chemically modified in diagnostic tests for the determination of cholesterol in combination with cholesterol oxidase. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; sterol esterase; CE. Cholesterol Esterase. Mole weight: ~129 kD. Activity: >10 U/mg lyophilizate; >100 U/mg protein. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; 9026-00-0; sterol esterase; CE. Cat No: DIA-281. | |
| Chemically modified Pseudomonas species Lipoprotein Lipase | Enzyme that hydrolyzes triglycerides into three free fatty acids and glycerol. Take advantage of the enhanced liquid stability of this enzyme. Rely on the proven diagnostic quality of this product. Applications: Use lipoprotein lipase in diagnostic tests for the determination of triglycerides together with glycerol kinase and glycerol-3-phosphate dehydrogenase. Group: Enzymes. Synonyms: Lipoprotein lipase; LPL; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. LPL. Mole weight: 47 kD. Activity: >10 U/mg lyophilizate. Stability: At +2 to +8°C within specification range for 12 months. Store dry. Appearance: Brownish lyophilizate. Source: Pseudomonas species. Lipoprotein lipase; LPL; EC 3.1.1.34; Clearing factor lipase; Diacylglycerol lipase; Diglyceride lipase. Cat No: DIA-282. | |
| Cholesterol Esterase from Pseudomonas sp. | Cholesterol esterase (CE) is also known as cholesterol ester hydrolase. This enzyme catalyzes the following reaction: Sterol Ester --------> Sterol + Fatty Acid. Cholesterol esterase activity has been demonstrated in pancreas, intestine, liver and kidney. The enzyme is inactivated by proteolytic enzymes but stabilized by proteolytic enzyme inhibitors and by bile salts. Group: Enzymes. Synonyms: cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Enzyme Commission Number: EC 3.1.1.13. CAS No. 9026-00-0. Activity: 100U/mg-solid or more (containing approx. 40% of stabilizers). Form: Freeze dried powder. Source: Pseudomonas sp. cholesterol esterase; cholesteryl ester synthase; triterpenol esterase; cholesteryl esterase; cholesteryl ester hydrolase; sterol ester hydrolase; cholesterol ester hydrolase; cholesterase; acylcholesterol lipase; EC 3.1.1.13; Sterol esterase. Cat No: DIA-134. | |
| Cholesterol esterase, Pseudomonas | Cholesterol esterase, Pseudomonas is an enzyme that hydrolyzes cholesterol ester to cholesterol and free fatty acid in the intestinal lumen. Cholesterol synthesized in the acinar cells and is stored in zymogen granules. Cholesterol esterase is also known as bile salt-stimulated lipase and carboxy ester lipasea, acts function for acceleration of cholesterol absorption [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9026-00-0. Pack Sizes: 100 U. Product ID: HY-P2879. | |
| Ciprofloxacin Hydrochloride, Monohydrate | Ciprofloxacin Hydrochloride is a high activity fluoroquinolone antibiotic effective against a broad spectrum of gram positive and negative bacteria such as Pseudomonas, Salmonella, streptococcus and Staphylococcus. Effective against mycoplasma (12 days). Ciprofloxacin differs from other quinolones in that it has a fluorine atom at the 6-position, a piperazine moiety at the 7-position, and a cyclopropyl ring at the 1-position. The bactericidal action of ciprofloxacin results from interference with the enzyme DNA gyrase which is needed for the synthesis of bacterial DNA. Ciprofloxacin has been shown to be active against most strains of the following organisms:Gram-Positive ...a typhi; Serratia marcescens; Shigella flexneri; Shigella sonnei; Vibrio cholerae; Vibrio parahaemolyticus; Vibrio vulnificus; Yersinia enterocolitica. Other Organisms:Chlamydia trachomatis (only moderately susceptible); Mycobacterium tuberculosis (only moderately susceptible).Also Available:C5075: Ciprofloxacin Hydrochloride 10mg/ml. Group: Biochemicals. Alternative Names: 1-Cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic Acid Hydrochloride; Bay Q3939 Hydrochloride. Grades: Molecular Biology Grade. CAS No. 86393-32-0. Pack Sizes: 1g, 10g, 25g, 50g. Molecular Formula: C17H18FN3O3 HCl H2O, Molecular Weight: 385.8. US Biological Life Sciences. | Worldwide |
| cobaltochelatase | This enzyme, which forms part of the aerobic cobalamin biosynthesis pathway, is a type I chelatase, being heterotrimeric and ATP-dependent. It comprises two components, one of which corresponds to CobN and the other is composed of two polypeptides, specified by cobS and cobT in Pseudomonas denitrificans, and named CobST. Hydrogenobyrinic acid is a very poor substrate. ATP can be replaced by dATP or CTP but the reaction proceeds more slowly. CobN exhibits a high affinity for hydrogenobyrinic acid a,c-diamide. The oligomeric protein CobST possesses at least one sulfhydryl group that is essential for ATP-binding. Once the Co2+ is inserted, the next step in the pathway ensures that the cobalt is ligated securely by reducing Co(II) to Co(I). This step is carried out by EC 1.16.8.1, cob(II)yrinic acid a,c-diamide reductase. Group: Enzymes. Synonyms: hydrogenobyrinic acid a,c-diamide cobaltochelatase; CobNST; CobNCobST. Enzyme Commission Number: EC 6.6.1.2. CAS No. 81295-49-0. 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-5828; cobaltochelatase; EC 6.6.1.2; 81295-49-0; hydrogenobyrinic acid a,c-diamide cobaltochelatase; CobNST; CobNCobST. Cat No: EXWM-5828. | |
| cob(I)yrinic acid a,c-diamide adenosyltransferase | The corrinoid adenosylation pathway comprises three steps: (I) reduction of Co(III) to Co(II) by a one-electron transfer. This can be carried out by EC 1.16.1.3, aquacobalamin reductase or non-enzymically in the presence of dihydroflavin nucleotides. (II) Co(II) is reduced to Co(I) in a second single-electron transfer by EC 1.16.1.4, cob(II)alamin reductase and (iII) the Co(I) conducts a nucleophilic attack on the adenosyl moiety of ATP to leave the cobalt atom in a Co(III) state (EC 2.5.1.17). The enzyme responsible for the adenosylation reaction is the product of the gene cobO in the aerobic bacterium Pseudomonas denitrificans and of the gene cobA in the anaerobic ...I)alamin adenosyltransferase; aquacob(I)alamin adenosyltransferase; aquocob(I)alamin vitamin B12s adenosyltransferase; ATP:cob(I)alamin Coβ-adenosyltransferase. Enzyme Commission Number: EC 2.5.1.17. CAS No. 37277-84-2. 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-2753; cob(I)yrinic acid a,c-diamide adenosyltransferase; EC 2.5.1.17; 37277-84-2; CobA; CobO; ATP:corrinoid adenosyltransferase; cob(I)alamin adenosyltransferase; aquacob(I)alamin adenosyltransferase; aquocob(I)alamin vitamin B12s adenosyltransferase; ATP:cob(I)alamin Coβ-adenosyltransferase. Cat No: EXWM-2753. | |
| Coronatine | It is produced by the strain of Pseudomonas coronafaciens, P. glycinea. It is a metabolite that is toxic to plants. Synonyms: 2-Ethyl-1-{[ (6-ethyl-1-oxo-2, 3, 3a, 6, 7, 7a-hexahydro-1H-inden-4-yl) (hydroxy) methylidene]amino}cyclopropane-1-carboxylic acid; (+)-coronatine. Grades: 95%. CAS No. 62251-96-1. Molecular formula: C18H25NO4. Mole weight: 319.40. | |
| CP 6232 | CP 6232 is a new anti-pseudomonal cephalosporin as a cell wall inhibitor. It was developed by Meiji Seika Pharma. Research for the treatment of bacterial infections was discontinued. Uses: Bacterial infections. Synonyms: CP 6232; CP6232; CP-6232. 7-((2-Aminothiazol-4-yl)-2-(1-carboxy-1-methyl)ethoxyiminoacetamido)-3-(N-(1,5-dihydroxy-4-pyridon-2-yl)methyl-N-methyl)aminomethyl-3-cephem-4-carboxylic acid. Grades: 98%. CAS No. 141562-38-1. Molecular formula: C24H27N7O10S2. Mole weight: 637.65. | |
| D-arginine dehydrogenase | Contains a non-covalent FAD cofactor. The enzyme, which has been isolated from the bacterium Pseudomonas aeruginosa PAO1, is a catabolic enzyme that is part of a two-enzyme complex involved in the racemization of D and L-arginine. The enzyme has a broad substrate range and can act on most D-amino acids with the exception of D-glutamate and D-aspartate. However, activity is maximal with D-arginine and D-lysine. Not active on glycine. Group: Enzymes. Synonyms: D-amino-acid:(acceptor) oxidoreductase (deaminating); D-amino-acid dehydrogenase; D-amino-acid:acceptor oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.99.6. CAS No. 37205-44-0. 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-1492; D-arginine dehydrogenase; EC 1.4.99.6; 37205-44-0; D-amino-acid:(acceptor) oxidoreductase (deaminating); D-amino-acid dehydrogenase; D-amino-acid:acceptor oxidoreductase (deaminating). Cat No: EXWM-1492. | |
| 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. | |
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