The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
Ethylene glycol (2-naphthyl) cyclopentylaminoethyl ether ID: ALA5290381
Chembl Id: CHEMBL5290381
Max Phase: Preclinical
Molecular Formula: C19H25NO2
Molecular Weight: 299.41
Associated Items:
Names and Identifiers Canonical SMILES: c1ccc2cc(OCCOCCNC3CCCC3)ccc2c1
Standard InChI: InChI=1S/C19H25NO2/c1-2-6-17-15-19(10-9-16(17)5-1)22-14-13-21-12-11-20-18-7-3-4-8-18/h1-2,5-6,9-10,15,18,20H,3-4,7-8,11-14H2
Standard InChI Key: ALEMZDSZUPOPRD-UHFFFAOYSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 299.41Molecular Weight (Monoisotopic): 299.1885AlogP: 3.77#Rotatable Bonds: 8Polar Surface Area: 30.49Molecular Species: BASEHBA: 3HBD: 1#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 3.75CX LogD: 1.21Aromatic Rings: 2Heavy Atoms: 22QED Weighted: 0.75Np Likeness Score: -0.73
References 1. Gao Y, Geng J, Xie Z, Zhou Z, Yang H, Yi H, Han X, Xue S, Li Z.. (2022) Synthesis and antineoplastic activity of ethylene glycol phenyl aminoethyl ether derivatives as FOXM1 inhibitors., 244 [PMID:36334454 ] [10.1016/j.ejmech.2022.114877 ]