ID: ALA5205691

Max Phase: Preclinical

Molecular Formula: C17H24Cl2N2

Molecular Weight: 254.38

Associated Items:

Representations

Canonical SMILES:  CC12CC3c4ccc(N)cc4C4CC(N)(C1)CC34C2.Cl.Cl

Standard InChI:  InChI=1S/C17H22N2.2ClH/c1-15-5-13-11-3-2-10(18)4-12(11)14-6-16(19,7-15)9-17(13,14)8-15;;/h2-4,13-14H,5-9,18-19H2,1H3;2*1H

Standard InChI Key:  VLUHMNGQHLXYIY-UHFFFAOYSA-N

Associated Targets(non-human)

Glutamate NMDA receptor 6467 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 254.38Molecular Weight (Monoisotopic): 254.1783AlogP: 3.13#Rotatable Bonds: 0
Polar Surface Area: 52.04Molecular Species: BASEHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.53CX LogP: 1.82CX LogD: -0.96
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.70Np Likeness Score: 0.95

References

1. Turcu AL, Companys-Alemany J, Phillips MB, Patel DS, Griñán-Ferré C, Loza MI, Brea JM, Pérez B, Soto D, Sureda FX, Kurnikova MG, Johnson JW, Pallàs M, Vázquez S..  (2022)  Design, synthesis, and in vitro and in vivo characterization of new memantine analogs for Alzheimer's disease.,  236  [PMID:35453065] [10.1016/j.ejmech.2022.114354]

Source