Compound ID | 2877

Update compound information

FL058/meropenem

Class: Beta-lactam + beta-lactamase inhibitor

Agent Type: Semisynthetic; Small molecule; Direct acting; Indirect acting;
Spectrum of activity: Gram-negative
Mechanism of action: Cell wall synthesis inhibitor. Inhibits class A, C, and some D beta-lactamases
Target Pathogen: Active against carbapenemase-producing Enterobacteriaceae
Combined with other compounds: Yes
Description: Synthetic compound
Institute where first reported: QiLu Pharmaceutical
Year first mentioned: 2023
Highest development stage: Phase 2 (NCT05060419)
Development status: Active as of 2024
Chemical structure(s):
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Molecular weight: 383.46
Iso. SMILES: C[C@@H]1[C@@H]2[C@H](C(=O)N2C(=C1S[C@H]3C[C@H](NC3)C(=O)N(C)C)C(=O)O)[C@@H](C)O
InChI Key: DMJNNHOOLUXYBV-PQTSNVLCSA-N
Can. SMILES: C[C@@H]1[C@@H]2[C@@H]([C@@H](C)O)C(=O)N2C(=C1S[C@H]3C[C@@H](C(=O)N(C)C)NC3)C(=O)O
InChI: InChI=1S/C17H25N3O5S/c1-7-12-11(8(2)21)16(23)20(12)13(17(24)25)14(7)26-9-5-10(18-6-9)15(22)19(3)4/h7-12,18,21H,5-6H2,1-4H3,(H,24,25)/t7-,8-,9+,10+,11-,12-/m1/s1
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/441130
Citation: https://journals.asm.org/doi/10.1128/aac.01330-23?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed

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