ID: ALA4789548

Max Phase: Preclinical

Molecular Formula: C10H12N2O3

Molecular Weight: 208.22

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCC(=O)Nc1ccccc1[N+](=O)[O-]

Standard InChI:  InChI=1S/C10H12N2O3/c1-2-5-10(13)11-8-6-3-4-7-9(8)12(14)15/h3-4,6-7H,2,5H2,1H3,(H,11,13)

Standard InChI Key:  QGQDJJOVVKDXOQ-UHFFFAOYSA-N

Associated Targets(non-human)

Transcriptional activator protein luxR 400 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 208.22Molecular Weight (Monoisotopic): 208.0848AlogP: 2.33#Rotatable Bonds: 4
Polar Surface Area: 72.24Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.10CX Basic pKa: CX LogP: 2.30CX LogD: 2.30
Aromatic Rings: 1Heavy Atoms: 15QED Weighted: 0.61Np Likeness Score: -1.89

References

1. Majik MS,Gawas UB,Mandrekar VK.  (2020)  Next generation quorum sensing inhibitors: Accounts on structure activity relationship studies and biological activities.,  28  (21): [PMID:33065436] [10.1016/j.bmc.2020.115728]

Source