ID: ALA3746396

Max Phase: Preclinical

Molecular Formula: C19H20N2O5

Molecular Weight: 356.38

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C19H20N2O5/c1-4-5-8-25-19(24)12-10-14(22)17(23)18-16(12)20-13-7-6-11(21(2)3)9-15(13)26-18/h6-7,9-10,23H,4-5,8H2,1-3H3

Standard InChI Key:  PSYPMXZRDFCVJO-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: 356.38Molecular Weight (Monoisotopic): 356.1372AlogP: 3.02#Rotatable Bonds: 5
Polar Surface Area: 92.87Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.47CX Basic pKa: 3.01CX LogP: 3.23CX LogD: 3.19
Aromatic Rings: 1Heavy Atoms: 26QED Weighted: 0.43Np Likeness Score: -0.43

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