ID: ALA96744

Max Phase: Preclinical

Molecular Formula: C18H21N3

Molecular Weight: 279.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C(#Cc1c[nH]cn1)CCN1CCC(c2ccccc2)CC1

Standard InChI:  InChI=1S/C18H21N3/c1-2-6-16(7-3-1)17-9-12-21(13-10-17)11-5-4-8-18-14-19-15-20-18/h1-3,6-7,14-15,17H,5,9-13H2,(H,19,20)

Standard InChI Key:  ZALGNZKPJDVGDG-UHFFFAOYSA-N

Associated Targets(non-human)

Grin3a Glutamate [NMDA] receptor subunit 3A (29 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin1 Glutamate NMDA receptor; Grin1/Grin2b (1028 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Grin2c Glutamate [NMDA] receptor subunit epsilon 3 (367 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: 279.39Molecular Weight (Monoisotopic): 279.1735AlogP: 3.03#Rotatable Bonds: 3
Polar Surface Area: 31.92Molecular Species: BASEHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.57CX Basic pKa: 8.66CX LogP: 3.22CX LogD: 1.93
Aromatic Rings: 2Heavy Atoms: 21QED Weighted: 0.88Np Likeness Score: -0.66

References

1. Wright JL, Gregory TF, Boxer PA, Meltzer LT, Serpa KA, Wise LD..  (1999)  Discovery of subtype-selective NMDA receptor ligands: 4-benzyl-1-piperidinylalkynylpyrroles, pyrazoles and imidazoles as NR1A/2B antagonists.,  (19): [PMID:10522697] [10.1016/s0960-894x(99)00482-5]

Source