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| Product | Description | |
|---|---|---|
| Acaterin | Acarbose is an acyl-CoA isolated from Pseudomonas species. A92. In the presence of oxidized low-density lipoprotein in macrophages J744, the synthesis of cholesterol enzymes is inhibited, with an IC50 of 45 μmol/L, and the IC50 for inhibiting ACAT in rat liver microsomes is 120 μmol/L. Inhibition of ACAT is non-competitive Sexual. Group: Pharmaceutical. CAS No. 144398-20-9. Pack Sizes: 1mg; 1g; 10g. Product ID: BBF-00539. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| Amikacin Impurities | Amikacin Impurities are integral in the biomedical sector for developing and refining quality assurance processes in pharmaceutical production. These impurities help identify the pharmacokinetic profile and stability of amikacin, an aminoglycoside antibiotic effective against serious bacterial infections, including those caused by resistant strains like Pseudomonas aeruginosa. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| 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. Group: Pharmaceutical. CAS No. 63358-49-6. Pack Sizes: 100 mg. Product ID: BBF-00569. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Cefiderocol | This active molecular is a potent cephalosporin antibiotic with a catechol moiety on the 3-position side chain under the development of Shionogi. Cefiderocol exhibits potent activity against the non-fermenting Gram-negative bacteria in vitro including Acinetobacter baumannii, Pseudomonas aeruginosa and Stenotrophomonas maltophilia. Now Cefiderocol is in clinical Phase III for treatment of severe infections caused by Carbapenem-resistant Gram-negative pathogens. Uses: Gram-negative infections. Group: Pharmaceutical. CAS No. 1225208-94-5. Pack Sizes: 1 mg. Product ID: B0084-475177. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Cefsulodin sodium | Cefsulodin is a third generation cephalosporin antibiotic designed specifically for Pseudomonas Aeruginosa. Uses: Anti-bacterial agents. Group: Pharmaceutical. CAS No. 52152-93-9. Pack Sizes: 5 g. Product ID: BBF-03891. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Ceftazidime Impurities | Ceftazidime Impurities are crucial in the biomedical sector for ensuring the quality and safety of the antibiotic ceftazidime. Monitoring these impurities aids in maintaining efficacy against bacterial infections, particularly Pseudomonas aeruginosa, and helps in compliance with pharmaceutical regulations, thereby safeguarding patient health during treatment. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| CHIR-090 | CHIR-090 is a very potent and tight-binding inhibitor of LpxC, which is a zinc-dependent amidase and present in almost all Gram-negative bacteria, and is a promising target for the development of novel antibiotic substances against multigrug-resistant Gram-negative bacteria. Its Ki value is 4.0 nM. It displays two-step time-dependent inhibition and kills a wide range of Gram-negative pathogens as effectively as ciprofloxacin or tobramycin. It has a different selectivity with the reported LpxC inhibitor L-161. It has excellent antibiotic activity against Pseudomonas aeruginosa and Escherichia coli by inhibiting LpxC orthologs at low nM concentrations. It is an excellent lead for the further development of new antibiotics targeting the lipid A pathway. Uses: Chir-090 displays two-step time-dependent inhibition and kills a wide range of gram-negative pathogens as effectively as ciprofloxacin or tobramycin. it has excellent antibiotic activity against pseudomonas aeruginosa and escherichia coli by inhibiting lpxc orthologs at low nm concentrations. Group: Pharmaceutical. CAS No. 728865-23-4. Pack Sizes: 300 mg. Product ID: B0084-474822. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| DB-2073 | DB-2073 is produced by the strain of Pseudomonas B-9004. It has the activity against streptococcus pneumoniae and tinea gypsum mold. Group: Pharmaceutical. CAS No. 39341-78-1. Pack Sizes: 100 mg. Product ID: BBF-02800. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| FR-901464 | It is a potent cell cycle inhibitor isolated from Pseudomonas sp. No.2663. It exhibits potent antitumor activities against tumor cell lines via binding to the spliceosome and modulating pre-mRNA splicing. Group: Pharmaceutical. CAS No. 146478-72-0. Pack Sizes: 1 mg. Product ID: BBF-04526. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Imipenem Monohydrate | Imipenem is an intravenous β-lactam antibiotic. It is the first member of the carbapenem class of antibiotics. Imipenem is discovered via a lengthy trial-and-error search for a more stable version of the natural product thienamycin, which is produced by the bacterium Streptomyces cattleya. Imipenem has a broad spectrum of activity against aerobic and anaerobic, Gram-positive and Gram-negative bacteria. It is particularly important for its activity against Pseudomonas aeruginosa and the Enterococcus species, but it is not active against MRSA. Uses: Anti-bacterial agents. Group: Pharmaceutical. CAS No. 74431-23-5. Pack Sizes: 500 mg. Product ID: BBF-04641. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Piperacillin sodium | Piperacillin is a semisynthetic, broad-spectrum, ampicillin derived ureidopenicillin antibiotic proposed for pseudomonas infections. Uses: Anti-bacterial agents. Group: Pharmaceutical. CAS No. 59703-84-3. Pack Sizes: 25 g. Product ID: BBF-03911. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Polymyxin B Impurities | Polymyxin B Impurities, derivatives arising during the synthesis of Polymyxin B, play a crucial role in the development of novel antibiotics. These impurities are vital for studying drug efficacy and safety, significantly advancing treatments for multidrug-resistant bacterial infections, including those caused by Pseudomonas aeruginosa and Acinetobacter baumannii. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Pyrrolnitrin | Pyrrolnitrin is a nitrogen-containing heterocyclic antibiotic produced by Pseudomonas pyrrocinia 2327. It has antifungal effect and weak anti-Gram-positive bacteria activity. Group: Pharmaceutical. CAS No. 1018-71-9. Pack Sizes: 1 mg. Product ID: BBF-02594. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tobramycin Impurities | Tobramycin impurities are crucial in the biomedical industry for developing and optimizing Tobramycin-based therapies. They serve as reference standards, ensuring quality control in the synthesis of Tobramycin, an aminoglycoside antibiotic used primarily to treat severe bacterial infections like Pseudomonas aeruginosa in cystic fibrosis and other resistant infections. Group: Pharmaceutical. Pack Sizes: 1mg; 1g; 10g. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
| Tubermycin B | A simple phenazine produced by several species of pseudomonas and actinomycetes. It is a weakly active antibacterial compound that plays a role in the biocontrol of plant diseases by several pseudomonas strains. Group: Pharmaceutical. CAS No. 2538-68-3. Pack Sizes: 250 mg. Product ID: BBF-03428. Molecular formula: Custom synthesis is available. Send your inquiries for more information. | London |
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