ID: ALA4435377

Max Phase: Preclinical

Molecular Formula: C9H15NO5S

Molecular Weight: 249.29

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCCC(=O)CS(=O)(=O)NC1CCOC1=O

Standard InChI:  InChI=1S/C9H15NO5S/c1-2-3-7(11)6-16(13,14)10-8-4-5-15-9(8)12/h8,10H,2-6H2,1H3

Standard InChI Key:  YKKDMAGMJTYQSG-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: 249.29Molecular Weight (Monoisotopic): 249.0671AlogP: -0.41#Rotatable Bonds: 6
Polar Surface Area: 89.54Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.73CX Basic pKa: CX LogP: -0.18CX LogD: -0.32
Aromatic Rings: 0Heavy Atoms: 16QED Weighted: 0.65Np Likeness Score: -0.27

References

1. Chbib C..  (2020)  Impact of the structure-activity relationship of AHL analogues on quorum sensing in Gram-negative bacteria.,  28  (3): [PMID:31918952] [10.1016/j.bmc.2019.115282]

Source