ID: ALA2431394

Max Phase: Preclinical

Molecular Formula: C22H20N4O

Molecular Weight: 356.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1nc2ccccc2n1CCC(=O)N/N=C/c1cccc2ccccc12

Standard InChI:  InChI=1S/C22H20N4O/c1-16-24-20-11-4-5-12-21(20)26(16)14-13-22(27)25-23-15-18-9-6-8-17-7-2-3-10-19(17)18/h2-12,15H,13-14H2,1H3,(H,25,27)/b23-15+

Standard InChI Key:  SATVOXLKEYIHSV-HZHRSRAPSA-N

Associated Targets(non-human)

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Caulobacter vibrioides 128 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 356.43Molecular Weight (Monoisotopic): 356.1637AlogP: 4.04#Rotatable Bonds: 5
Polar Surface Area: 59.28Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.84CX Basic pKa: 6.17CX LogP: 3.64CX LogD: 3.62
Aromatic Rings: 4Heavy Atoms: 27QED Weighted: 0.43Np Likeness Score: -1.97

References

1. Zhou M, Eun YJ, Guzei IA, Weibel DB..  (2013)  Structure-activity studies of divin: an inhibitor of bacterial cell division.,  (9): [PMID:24044050] [10.1021/ml400234x]

Source