ID: ALA2387706

Max Phase: Preclinical

Molecular Formula: C27H37N5O2

Molecular Weight: 463.63

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCN(CCN1CCN(c2ccccc2OC)CC1)C1CCc2cc3[nH]c(=O)[nH]c3cc2C1

Standard InChI:  InChI=1S/C27H37N5O2/c1-3-10-31(22-9-8-20-18-23-24(19-21(20)17-22)29-27(33)28-23)14-11-30-12-15-32(16-13-30)25-6-4-5-7-26(25)34-2/h4-7,18-19,22H,3,8-17H2,1-2H3,(H2,28,29,33)

Standard InChI Key:  IPIVRQVYRNSMML-UHFFFAOYSA-N

Associated Targets(non-human)

Dopamine D3 receptor 1050 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Dopamine D2 receptor 7893 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: 463.63Molecular Weight (Monoisotopic): 463.2947AlogP: 3.26#Rotatable Bonds: 8
Polar Surface Area: 67.60Molecular Species: BASEHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.85CX Basic pKa: 9.67CX LogP: 4.40CX LogD: 2.15
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.54Np Likeness Score: -1.16

References

1. Gopishetty B, Zhang S, Kharkar PS, Antonio T, Reith M, Dutta AK..  (2013)  Modification of agonist binding moiety in hybrid derivative 5/7-{[2-(4-aryl-piperazin-1-yl)-ethyl]-propyl-amino}-5,6,7,8-tetrahydro-naphthalen-1-ol/-2-amino versions: impact on functional activity and selectivity for dopamine D2/D3 receptors.,  21  (11): [PMID:23623679] [10.1016/j.bmc.2013.03.059]

Source