ID: ALA3764884

Max Phase: Preclinical

Molecular Formula: C20H22F3N5OS2

Molecular Weight: 469.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c(SCCCN2CCOC(c3ccc(C(F)(F)F)cc3)C2)nnc1-c1nccs1

Standard InChI:  InChI=1S/C20H22F3N5OS2/c1-27-17(18-24-7-12-30-18)25-26-19(27)31-11-2-8-28-9-10-29-16(13-28)14-3-5-15(6-4-14)20(21,22)23/h3-7,12,16H,2,8-11,13H2,1H3

Standard InChI Key:  LSTIDGGQGHFYCB-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: 469.56Molecular Weight (Monoisotopic): 469.1218AlogP: 4.51#Rotatable Bonds: 7
Polar Surface Area: 56.07Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.81CX LogP: 3.91CX LogD: 3.81
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.37Np Likeness Score: -2.21

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