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900814-48-4

900814-48-4 Structure

900814-48-4 Structure
IdentificationBack Directory
[Name]

N-[2-[[(1S)-2'-(3-Methylbutoxy)[1,1'-binaphthalen]-2-yl]oxy]acetyl]-D-lysyl-D-arginyl-L-leucine 3-methylbutyl ester hydrochloride
[CAS]

900814-48-4
[Synonyms]

CS-879
CS-1218
AVX 13616
Isopentyl (2-(((S)-2'-(isopentyloxy)-[1,1'-binaphthalen]-2-yl)oxy)acetyl)-D-lysyl-D-arginyl-L-leucinate dihydrochloride
N-[2-[[(1S)-2'-(3-Methylbutoxy)[1,1'-binaphthalen]-2-yl]oxy]acetyl]-D-lysyl-D-arginyl-L-leucine 3-methylbutyl ester hydrochloride
N-[2-[[(1S)-2'-(3-Methylbutoxy)[1,1'-binaphthalen]-2-yl]oxy]acetyl]-D-lysyl-D-arginyl-L-leucine 3-methylbutyl ester hydrochloride USP/EP/BP
[Molecular Formula]

C50H71N7O7.2(HCl)
[MDL Number]

MFCD28053484
[MOL File]

900814-48-4.mol
[Molecular Weight]

919
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
[form ]

Powder
Hazard InformationBack Directory
[Uses]

AVX 13616 shows the potent in vivo antibacterial activity of Avexa’s lead antibacterial candidate; particularly against drug-resistant Staphylococcus pathogens. IC50 value: 2-4 ug/ml (MICs) Target: antibacterial agent AVX13616 was as active as mupirocin in a nasal decolonization model but required only a single application. The compounds are being developed for topical indications and/or wound infection/catheter-related infections. AVX13616 and other compounds showed broad spectrum antibacterial activity against a range of isolates with MICs of 2-4 micrograms per millilitre against S. aureus, coagulase negative staphylococci, enterococci, MRSA, VISA and VRSA. A single application of 5% (w/w) AVX13616 (approximately equimolar to 2% mupirocin) was as effective as 2% mupirocin administered twice a day for five days in nasal decolonisation of MRSA in mice.
[References]

[1] Avexa Presents Data from Apricitabine and Antibacterial Programs at two International Conferences
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