Compound ID | 1958
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/ |