Compound ID | 202

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DNAC-1

Class: Small molecule antibacterial agent

Agent Type: Synthetic; Small molecule; Direct acting;
Spectrum of activity: Gram-negative
Mechanism of action: Membrane-active agent. Additionally causes mislocalisation of FtsZ, PBP2, and PBP4; cell wall synthesis inhibitor
Target Pathogen: Active against methicillin-resistant Staphylococcus aureus
Combined with other compounds: Yes
Propensity to select resistant mutants: Yes
Description: Synthetic compound from ICCB-Longwood Screening Facility (New England Regional Centers of Excellence) small molecule collection; a quinolinol derivative; potentiates beta-lactams; shows no toxicity to mammalian cells
Institute where first reported: Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA
Year first mentioned: 2015
Development status: Experimental
Chemical structure(s):
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Molecular weight: 313.24
Iso. SMILES: CC1=C(SC2=C1C(=C(S2)Br)C)C3=CC=NN3
InChI Key: MUNXAASMRMRSCE-UHFFFAOYSA-N
Can. SMILES: CC1=C(C2=CC=NN2)SC3=C1C(=C(Br)S3)C
InChI: InChI=1S/C11H9BrN2S2/c1-5-8-6(2)10(12)16-11(8)15-9(5)7-3-4-13-14-7/h3-4H,1-2H3,(H,13,14)
External links:
PubChem link: https://pubchem.ncbi.nlm.nih.gov/compound/2820501
Citations:
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621627/
  • http://aac.asm.org/content/59/4/1876.full

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