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| Product | Description | |
|---|---|---|
| Tobramycin | Tobramycin is an aminoglycoside antibiotic with an IC50 of 9.7 μM. Group: Pharmaceutical. CAS No. 32986-56-4. Pack Sizes: 1 g. Product ID: BBF-04568. Molecular formula: Custom synthesis is available. Send your inquiries for more information. |  London |
| Tobramycin Base | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C18H37N5O9. CAS No. 32986-56-4. Prepack ID : 76303024-1g. Molecular Weight : 467.51. |  |
| Tobramycin Base | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C18H37N5O9. CAS No. 32986-56-4. Prepack ID : 76303024-5g. Molecular Weight : 467.51. | |
| 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 |
| Tobramycin sulfate | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: (C18H37N5O9)2 ¢5H2SO4. CAS No. 49842-07-1. Prepack ID : 89988554-1g. Molecular Weight : 1425.41. | |
| 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 |
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