ID: ALA3764639

Max Phase: Preclinical

Molecular Formula: C24H24F3N5OS

Molecular Weight: 487.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c(SCCCN2CCOC(c3ccc(C(F)(F)F)cc3)C2)nnc1-c1ccc(C#N)cc1

Standard InChI:  InChI=1S/C24H24F3N5OS/c1-31-22(19-5-3-17(15-28)4-6-19)29-30-23(31)34-14-2-11-32-12-13-33-21(16-32)18-7-9-20(10-8-18)24(25,26)27/h3-10,21H,2,11-14,16H2,1H3

Standard InChI Key:  RWOJEGLVFGCYFU-UHFFFAOYSA-N

Associated Targets(Human)

Dopamine D3 receptor 14368 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Dopamine D2 receptor 23596 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HERG 29587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Dopamine D3 receptor 1050 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: 487.55Molecular Weight (Monoisotopic): 487.1654AlogP: 4.93#Rotatable Bonds: 7
Polar Surface Area: 66.97Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.84CX LogP: 4.73CX LogD: 4.62
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.35Np Likeness Score: -2.12

References

1. Micheli F, Cremonesi S, Semeraro T, Tarsi L, Tomelleri S, Cavanni P, Oliosi B, Perdonà E, Sava A, Zonzini L, Feriani A, Braggio S, Heidbreder C..  (2016)  Novel morpholine scaffolds as selective dopamine (DA) D3 receptor antagonists.,  26  (4): [PMID:26786693] [10.1016/j.bmcl.2015.12.081]

Source