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2427626-11-5

2427626-11-5 Structure

2427626-11-5 Structure
IdentificationBack Directory
[Name]

3-Azabicyclo[3.1.0]hexane-3-ethanol, 6-[2-[4-[3-[(1R)-2-amino-1-[2-[(1S)-1-hydroxyethyl]-1H-imidazol-1-yl]ethyl]-5-isoxazolyl]phenyl]ethynyl]-α-methyl-, (αS,1α,1α,5α,5α,6-exo,6α,6β)-
[CAS]

2427626-11-5
[Synonyms]

TP0586352
3-Azabicyclo[3.1.0]hexane-3-ethanol, 6-[2-[4-[3-[(1R)-2-amino-1-[2-[(1S)-1-hydroxyethyl]-1H-imidazol-1-yl]ethyl]-5-isoxazolyl]phenyl]ethynyl]-α-methyl-, (αS,1α,1α,5α,5α,6-exo,6α,6β)-
[Molecular Formula]

C26H31N5O3
[MOL File]

2427626-11-5.mol
[Molecular Weight]

461.57
Chemical PropertiesBack Directory
[Boiling point ]

697.8±55.0 °C(Predicted)
[density ]

1.37±0.1 g/cm3(Predicted)
[pka]

13.57±0.20(Predicted)
Hazard InformationBack Directory
[Description]

TP0586352 is a novel non-hydroxamate LpxC inhibitor, being effective against carbapenem-resistant Klebsiella pneumoniae without posing a cardiovascular risk.
[Uses]

TP0586352 is a LpxC inhibitor that is effective against carbapenem-resistant Klebsiella pneumoniae and does not pose a cardiovascular risk. TP0586352 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
[References]

[1] Ushiyama F, et al. Lead optimization of 2-hydroxymethyl imidazoles as non-hydroxamate LpxC inhibitors: Discovery of TP0586532. Bioorg Med Chem. 2021 Jan 15;30:115964. DOI:10.1016/j.bmc.2020.115964
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