epetraborole   Click here for help

GtoPdb Ligand ID: 13079

Synonyms: AN3365 | GSK2251052
Compound class: Synthetic organic
Comment: Epetraborole (GSK2251052) is an aminomethylbenzoxaborole antibacterial compound that is an inhibitor of bacterial leucyl-tRNA synthetase (LeuRS) [2]. It is being developed for the treatment of non-tuberculous mycobacterial pulmonary disease (NTM-PD).
2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 5
Hydrogen bond donors 3
Rotatable bonds 5
Topological polar surface area 84.94
Molecular weight 237.06
XLogP -0.83
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES C1=CC(=C2C(=C1)[C@@H](CN)OB2O)OCCCO
Isomeric SMILES B1(C2=C(C=CC=C2OCCCO)[C@H](O1)CN)O
InChI InChI=1S/C11H16BNO4/c13-7-10-8-3-1-4-9(16-6-2-5-14)11(8)12(15)17-10/h1,3-4,10,14-15H,2,5-7,13H2/t10-/m1/s1
InChI Key FXQIIDINBDJDKL-SNVBAGLBSA-N
References
1. Ganapathy US, Gengenbacher M, Dick T. (2021)
Epetraborole Is Active against Mycobacterium abscessus.
Antimicrob Agents Chemother, 65 (10): e0115621. [PMID:34280020]
2. Hernandez V, Crépin T, Palencia A, Cusack S, Akama T, Baker SJ, Bu W, Feng L, Freund YR, Liu L et al.. (2013)
Discovery of a novel class of boron-based antibacterials with activity against gram-negative bacteria.
Antimicrob Agents Chemother, 57 (3): 1394-403. [PMID:23295920]
3. O'Dwyer K, Spivak AT, Ingraham K, Min S, Holmes DJ, Jakielaszek C, Rittenhouse S, Kwan AL, Livi GP, Sathe G et al.. (2015)
Bacterial resistance to leucyl-tRNA synthetase inhibitor GSK2251052 develops during treatment of complicated urinary tract infections.
Antimicrob Agents Chemother, 59 (1): 289-98. [PMID:25348524]