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Ancremonam

Catalog No. T27962   CAS 1810051-96-7
Synonyms: LYS228, LYS-228, LYS 228

LYS228 is a potent antibiotics against Carbapenem-Resistant Enterobacteriaceae (MIC90 = 2 uM/mL). LYS228 is potent in the presence of all classes of beta-lactamases.

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Ancremonam Chemical Structure
Ancremonam, CAS 1810051-96-7
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Biological Description
Chemical Properties
Storage & Solubility Information
Description LYS228 is a potent antibiotics against Carbapenem-Resistant Enterobacteriaceae (MIC90 = 2 uM/mL). LYS228 is potent in the presence of all classes of beta-lactamases.
Synonyms LYS228, LYS-228, LYS 228
Molecular Weight 518.48
Formula C16H18N6O10S2
CAS No. 1810051-96-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

TargetMolReferences and Literature

1. Klingen AR, Palsdottir H, Hunte C, Ullmann GM. Redox-linked protonation state changes in cytochrome bc1 identified by Poisson-Boltzmann electrostatics calculations. Biochim Biophys Acta. 2007 Mar;1767(3):204-21. Epub 2007 Jan 31. PubMed PMID: 17349966. 2. Rosell A, Valencia E, Ochoa WF, Fita I, Parés X, Farrés J. Complete reversal of coenzyme specificity by concerted mutation of three consecutive residues in alcohol dehydrogenase. J Biol Chem. 2003 Oct 17;278(42):40573-80. Epub 2003 Aug 4. PubMed PMID: 12902331. 3. Rosell A, Valencia E, Parés X, Fita I, Farrés J, Ochoa WF. Crystal structure of the vertebrate NADP(H)-dependent alcohol dehydrogenase (ADH8). J Mol Biol. 2003 Jun 27;330(1):75-85. PubMed PMID: 12818203. 4. Shimizu T, Nakatsu T, Miyairi K, Okuno T, Kato H. Active-site architecture of endopolygalacturonase I from Stereum purpureum revealed by crystal structures in native and ligand-bound forms at atomic resolution. Biochemistry. 2002 May 28;41(21):6651-9. PubMed PMID: 12022868.

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

Ancremonam 1810051-96-7 LYS228 LYS-228 LYS 228 inhibitor inhibit

 

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