ID: ALA4851675

Max Phase: Preclinical

Molecular Formula: C18H21FN2O4

Molecular Weight: 348.37

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(N(C)C(=O)N(C)c2cccc(F)c2)cc(OC)c1OC

Standard InChI:  InChI=1S/C18H21FN2O4/c1-20(13-8-6-7-12(19)9-13)18(22)21(2)14-10-15(23-3)17(25-5)16(11-14)24-4/h6-11H,1-5H3

Standard InChI Key:  ASQUXQIKDLVTLJ-UHFFFAOYSA-N

Associated Targets(Human)

Daoy 570 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

ONS-76 191 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: 348.37Molecular Weight (Monoisotopic): 348.1485AlogP: 3.54#Rotatable Bonds: 5
Polar Surface Area: 51.24Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 2.52CX LogD: 2.52
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.83Np Likeness Score: -0.90

References

1. Lawson C, Ahmed Alta TB, Moschou G, Skamnaki V, Solovou TGA, Topham C, Hayes J, Snape TJ..  (2021)  Novel diarylamides and diarylureas with N-substitution dependent activity against medulloblastoma.,  225  [PMID:34391032] [10.1016/j.ejmech.2021.113751]

Source