ID: ALA3746248

Max Phase: Preclinical

Molecular Formula: C18H18N2O6

Molecular Weight: 358.35

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COCCOC(=O)c1cc(=O)c(O)c2oc3cc(N(C)C)ccc3nc1-2

Standard InChI:  InChI=1S/C18H18N2O6/c1-20(2)10-4-5-12-14(8-10)26-17-15(19-12)11(9-13(21)16(17)22)18(23)25-7-6-24-3/h4-5,8-9,22H,6-7H2,1-3H3

Standard InChI Key:  NWQSTCXOUUHHEL-UHFFFAOYSA-N

Associated Targets(Human)

Dickkopf-related protein 1/Low-density lipoprotein receptor-related protein 6 20 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Dickkopf-related protein 1/Lrp6 9 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: 358.35Molecular Weight (Monoisotopic): 358.1165AlogP: 1.87#Rotatable Bonds: 5
Polar Surface Area: 102.10Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.36CX Basic pKa: 3.01CX LogP: 1.86CX LogD: 1.81
Aromatic Rings: 1Heavy Atoms: 26QED Weighted: 0.42Np Likeness Score: -0.58

References

1. Mpousis S, Thysiadis S, Avramidis N, Katsamakas S, Efthimiopoulos S, Sarli V..  (2016)  Synthesis and evaluation of gallocyanine dyes as potential agents for the treatment of Alzheimer's disease and related neurodegenerative tauopathies.,  108  [PMID:26629858] [10.1016/j.ejmech.2015.11.024]

Source