1-(4-fluorophenyl)-1,3-dimethyl-3-(3,4,5-trimethoxyphenyl)urea

ID: ALA4866034

Chembl Id: CHEMBL4866034

PubChem CID: 164625582

Max Phase: Preclinical

Molecular Formula: C18H21FN2O4

Molecular Weight: 348.37

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(N(C)C(=O)N(C)c2ccc(F)cc2)cc(OC)c1OC

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

Standard InChI Key:  LSIMZLOSWWXABB-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4866034

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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

Calculated Properties

Molecular Weight: 348.37Molecular Weight (Monoisotopic): 348.1485AlogP: 3.54#Rotatable Bonds: 5
Polar Surface Area: 51.24Molecular Species: NEUTRALHBA: 4HBD:
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.52CX LogD: 2.52
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.83Np Likeness Score: -0.77

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