N,N,9-trimethyl-2-nitro-5,6,8,9,10,11-hexahydro-7H-5,9:7,11-dimethanobenzo[9]annulen-7-amine hydrochloride

ID: ALA5187377

Chembl Id: CHEMBL5187377

PubChem CID: 168279646

Max Phase: Preclinical

Molecular Formula: C19H25ClN2O2

Molecular Weight: 312.41

Associated Items:

Names and Identifiers

Canonical SMILES:  CN(C)C12CC3c4cc([N+](=O)[O-])ccc4C4CC(C)(CC43C1)C2.Cl

Standard InChI:  InChI=1S/C19H24N2O2.ClH/c1-17-7-15-13-5-4-12(21(22)23)6-14(13)16-8-18(9-17,20(2)3)11-19(15,16)10-17;/h4-6,15-16H,7-11H2,1-3H3;1H

Standard InChI Key:  CRLHVLYMFDQWKV-UHFFFAOYSA-N

Associated Targets(non-human)

Grin1 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

Calculated Properties

Molecular Weight: 312.41Molecular Weight (Monoisotopic): 312.1838AlogP: 4.06#Rotatable Bonds: 2
Polar Surface Area: 46.38Molecular Species: BASEHBA: 3HBD:
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 10.45CX LogP: 3.40CX LogD: 0.49
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.61Np Likeness Score: -0.05

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