ID: ALA1743987

Max Phase: Preclinical

Molecular Formula: C12H14Cl2N4

Molecular Weight: 248.72

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cl.Clc1ccc2nc(N3CCNCC3)cnc2c1

Standard InChI:  InChI=1S/C12H13ClN4.ClH/c13-9-1-2-10-11(7-9)15-8-12(16-10)17-5-3-14-4-6-17;/h1-2,7-8,14H,3-6H2;1H

Standard InChI Key:  DDOUKHPYRWZNCX-UHFFFAOYSA-N

Associated Targets(non-human)

Serotonin (5-HT) receptor 353 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Serotonin transporter 6087 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rattus norvegicus 775804 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: 248.72Molecular Weight (Monoisotopic): 248.0829AlogP: 1.69#Rotatable Bonds: 1
Polar Surface Area: 41.05Molecular Species: BASEHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 8.75CX LogP: 2.07CX LogD: 0.71
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.83Np Likeness Score: -1.81

References

1. Lumma WC, Hartman RD, Saari WS, Engelhardt EL, Lotti VJ, Stone CA..  (1981)  Piperazinylquinoxalines with central serotoninmimetic activity.,  24  (1): [PMID:6451700] [10.1021/jm00133a019]

Source