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BAL30072
CAS No. 941285-15-0
BAL30072( BAL 30072 )
Catalog No. M16733 CAS No. 941285-15-0
BAL30072 is a monocyclic beta-lactam antibiotic that shows potent activity against MDR Pseudomonas aeruginosa and Acinetobacter sp.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 873 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
| 5MG | 873 | Get Quote |
|
| 100MG | Get Quote | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameBAL30072
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NoteResearch use only, not for human use.
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Brief DescriptionBAL30072 is a monocyclic beta-lactam antibiotic that shows potent activity against MDR Pseudomonas aeruginosa and Acinetobacter sp.
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DescriptionBAL30072 is a monocyclic beta-lactam antibiotic that shows potent activity against MDR Pseudomonas aeruginosa and Acinetobacter sp. Isolates with MIC90 of 8 and 4 ug/ml; BAL30072 is also active against many species of MDR isolates of the Enterobacteriaceae family, including isolates that had a class A carbapenemase or a metallo-beta-lactamase; trigger the spheroplasting and lysis of Escherichia coli rather than the formation of extensive filaments.Bacterial Infection Phase 1 Clinical.
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In Vitro——
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In Vivo——
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SynonymsBAL 30072
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PathwayGPCR/G Protein
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TargetAntibacterial
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RecptorAntibacterial
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Research AreaInfection
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IndicationBacterial Infection
Chemical Information
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CAS Number941285-15-0
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Formula Weight518.472
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Molecular FormulaC16H18N6O10S2
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Purity>98% (HPLC)
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Solubility——
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SMILESCC1([C@@H](C(=O)N1OS(=O)(=O)O)NC(=O)/C(=N\OCc2cc(=O)c(cn2O)O)/c3csc(n3)N)C
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Chemical Name(aZ)-2-Amino-a-[[(1,4-dihydro-1,5-dihydroxy-4-oxo-2-pyridinyl)methoxy]imino]-N-[(3S)-2,2-dimethyl-4-oxo-1-(sulfooxy)-3-azetidinyl]-4-thiazoleacetamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Page MG, et al. Antimicrob Agents Chemother. 2010 Jun;54(6):2291-302.
2. Russo TA, et al. J Antimicrob Chemother. 2011 Apr;66(4):867-73.
3. Mima T, et al. Int J Antimicrob Agents. 2011 Aug;38(2):157-9.
4. Hornsey M, et al. Int J Antimicrob Agents. 2013 Oct;42(4):343-6.
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