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Ethylene glycol (2-benzyloxyphenyl) cyclopentylaminoethyl ether ID: ALA5273521
Chembl Id: CHEMBL5273521
Max Phase: Preclinical
Molecular Formula: C22H29NO3
Molecular Weight: 355.48
Associated Items:
Names and Identifiers Canonical SMILES: c1ccc(COc2ccccc2OCCOCCNC2CCCC2)cc1
Standard InChI: InChI=1S/C22H29NO3/c1-2-8-19(9-3-1)18-26-22-13-7-6-12-21(22)25-17-16-24-15-14-23-20-10-4-5-11-20/h1-3,6-9,12-13,20,23H,4-5,10-11,14-18H2
Standard InChI Key: WIKKDDOCAIXZKS-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: 355.48Molecular Weight (Monoisotopic): 355.2147AlogP: 4.19#Rotatable Bonds: 11Polar Surface Area: 39.72Molecular Species: BASEHBA: 4HBD: 1#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 4.33CX LogD: 1.79Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.61Np Likeness Score: -0.63
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 ]