3-({[(4-Oxo-4H-chromen-2-yl)carbonyl]amino}ethyl)phenylethyl(methyl)carbamate

ID: ALA4173608

Chembl Id: CHEMBL4173608

PubChem CID: 145950384

Max Phase: Preclinical

Molecular Formula: C22H22N2O5

Molecular Weight: 394.43

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCN(C)C(=O)Oc1cccc(CCNC(=O)c2cc(=O)c3ccccc3o2)c1

Standard InChI:  InChI=1S/C22H22N2O5/c1-3-24(2)22(27)28-16-8-6-7-15(13-16)11-12-23-21(26)20-14-18(25)17-9-4-5-10-19(17)29-20/h4-10,13-14H,3,11-12H2,1-2H3,(H,23,26)

Standard InChI Key:  TWEUHVZHTLEEIL-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4173608

    ---

Associated Targets(Human)

CHRNE Tclin Acetylcholine receptor protein epsilon chain (95 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
APP Tclin Amyloid-beta A4 protein (8510 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

HT-22 (3261 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: 394.43Molecular Weight (Monoisotopic): 394.1529AlogP: 3.22#Rotatable Bonds: 6
Polar Surface Area: 88.85Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 2.80CX LogD: 2.80
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.69Np Likeness Score: -0.83

References

1. Nesi G, Chen Q, Sestito S, Digiacomo M, Yang X, Wang S, Pi R, Rapposelli S..  (2017)  Nature-based molecules combined with rivastigmine: A symbiotic approach for the synthesis of new agents against Alzheimer's disease.,  141  [PMID:29031070] [10.1016/j.ejmech.2017.10.006]

Source