ChemicalBook--->CAS DataBase List--->1452458-86-4

1452458-86-4

1452458-86-4 Structure

1452458-86-4 Structure
IdentificationBack Directory
[Name]

OP-0595
[CAS]

1452458-86-4
[Synonyms]

OP-0595
OP0595 free acid
Sulfuric acid, mono[(1R,2S,5R)-2-[[(2-aminoethoxy)amino]carbonyl]-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl] ester
[Molecular Formula]

C9H16N4O7S
[MDL Number]

MFCD28986228
[MOL File]

1452458-86-4.mol
[Molecular Weight]

324.31
Chemical PropertiesBack Directory
[density ]

1.71±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C, protect from light, stored under nitrogen
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

-4.59±0.18(Predicted)
[color ]

White to light brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

Nacubactam (OP0595 free acid) is a potent non-β-lactam-β-lactamase inhibitor with activity against class A and class C β-lactamases. Nacubactam (OP0595 free acid) acts as a penicillin binding protein (PBP) 2-active antibacterial, and gives β-lactamase-independent potentiation of β-lactams targeting other PBPs[1][2].
[References]

[1] Monogue ML, et al. In Vivo Efficacy of Meropenem with a Novel Non-β-Lactam-β-Lactamase Inhibitor, Nacubactam, against Gram-Negative Organisms Exhibiting Various Resistance Mechanisms in a Murine Complicated Urinary Tract Infection Model. Antimicrob Agents Chemother. 2018 Aug 27;62(9). DOI:10.1128/AAC.02596-17
[2] Livermore DM, et al. Activity of OP0595/β-lactam combinations against Gram-negative bacteria with extended-spectrum, AmpC and carbapenem-hydrolysing β-lactamases. J Antimicrob Chemother. 2015 Nov;70(11):3032-41. DOI:10.1093/jac/dkv239
Spectrum DetailBack Directory
[Spectrum Detail]

OP-0595(1452458-86-4)1HNMR
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