Compound ID | 1958

Durlobactam

Synonym(s): ETX-2514  |  ETX2514

Class: Beta-lactamase inhibitor (non-beta-lactam beta-lactamase inhibitor, diazabicyclooctane [DBO])

Details of activity: DBOs bind reversibly to the beta-lactamase in the active site, inhibits class A, C, D and weakly inhibits penicillin binding protein 2 in Enterobacteriaceae
Combined with other compounds: Yes
Description: Synthetic compound. In clinical development in fixed combination with Sulbactam against Acinetobacter infections.
Institute where first reported: Entasis Therapeutics, Innoviva
Year first mentioned: 2017
Highest developmental phase: Phase 3 (NCT03894046)
Development status: Active (as of 2022)
Chemical structure(s):
Canonical SMILES: CC1=C[C@@H]2CN([C@@H]1C(=O)N)C(=O)N2OS(=O)(=O)O
Isomeric SMILES: CC1=C[C@@H]2CN([C@@H]1C(=O)N)C(=O)N2OS(=O)(=O)O
InChI: InChI=1S/C8H11N3O6S/c1-4-2-5-3-10(6(4)7(9)12)8(13)11(5)17-18(14,15)16/h2,5-6H,3H2,1H3,(H2,9,12)(H,14,15,16)/t5-,6+/m1/s1
InChI Key: BISPBXFUKNXOQY-RITPCOANSA-N
Structure link: https://pubchem.ncbi.nlm.nih.gov/compound/89851852
External links:
Guide to Pharmacology: durlobactam
Main Source: https://pubmed.ncbi.nlm.nih.gov/28835096/

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