N-(3-(4-(2-ethoxyphenyl)piperazin-1-yl)propyl)isonicotinamide

ID: ALA3764534

Chembl Id: CHEMBL3764534

PubChem CID: 127042300

Max Phase: Preclinical

Molecular Formula: C21H28N4O2

Molecular Weight: 368.48

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOc1ccccc1N1CCN(CCCNC(=O)c2ccncc2)CC1

Standard InChI:  InChI=1S/C21H28N4O2/c1-2-27-20-7-4-3-6-19(20)25-16-14-24(15-17-25)13-5-10-23-21(26)18-8-11-22-12-9-18/h3-4,6-9,11-12H,2,5,10,13-17H2,1H3,(H,23,26)

Standard InChI Key:  WQYZLMWFSUJAHL-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3764534

    ---

Associated Targets(non-human)

Htr1a Serotonin 1a (5-HT1a) receptor (8655 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Htr2a Serotonin 2a (5-HT2a) receptor (3540 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Htr2c Serotonin 2c (5-HT2c) receptor (1134 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

Calculated Properties

Molecular Weight: 368.48Molecular Weight (Monoisotopic): 368.2212AlogP: 2.42#Rotatable Bonds: 8
Polar Surface Area: 57.70Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.55CX LogP: 1.85CX LogD: 1.47
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.73Np Likeness Score: -1.69

References

1. Fiorino F, Ciano A, Magli E, Severino B, Corvino A, Perissutti E, Frecentese F, Di Vaio P, Izzo AA, Capasso R, Massarelli P, Nencini C, Rossi I, Kędzierska E, Orzelska-Gòrka J, Bielenica A, Santagada V, Caliendo G..  (2016)  Synthesis, in vitro and in vivo pharmacological evaluation of serotoninergic ligands containing an isonicotinic nucleus.,  110  [PMID:26820556] [10.1016/j.ejmech.2016.01.021]

Source