ID: ALA2140403

Max Phase: Preclinical

Molecular Formula: C22H20N2O

Molecular Weight: 328.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C2=NN(c3ccccc3)C(c3ccccc3)C2)cc1

Standard InChI:  InChI=1S/C22H20N2O/c1-25-20-14-12-17(13-15-20)21-16-22(18-8-4-2-5-9-18)24(23-21)19-10-6-3-7-11-19/h2-15,22H,16H2,1H3

Standard InChI Key:  IIWCGGYOWGNBJS-UHFFFAOYSA-N

Associated Targets(non-human)

Botulinum neurotoxin type A 238 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botulinum neurotoxin type F 132 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Anthrax lethal factor 7585 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: 328.42Molecular Weight (Monoisotopic): 328.1576AlogP: 5.05#Rotatable Bonds: 4
Polar Surface Area: 24.83Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 4.76CX LogP: 5.26CX LogD: 5.26
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.67Np Likeness Score: -1.10

References

1. PubChem BioAssay data set, 

Source

Source(1):