ID: ALA3746859

Max Phase: Preclinical

Molecular Formula: C18H18N2O5

Molecular Weight: 342.35

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C18H18N2O5/c1-9(2)24-18(23)11-8-13(21)16(22)17-15(11)19-12-6-5-10(20(3)4)7-14(12)25-17/h5-9,22H,1-4H3

Standard InChI Key:  YHODKBAKTVYPDY-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: 342.35Molecular Weight (Monoisotopic): 342.1216AlogP: 2.63#Rotatable Bonds: 3
Polar Surface Area: 92.87Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.53CX Basic pKa: 3.01CX LogP: 2.68CX LogD: 2.65
Aromatic Rings: 1Heavy Atoms: 25QED Weighted: 0.58Np Likeness Score: -0.57

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