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Ethylene glycol (4-(2-nitro)benzyloxyphenyl) cyclopentylaminoethyl ether ID: ALA5275595
Chembl Id: CHEMBL5275595
Max Phase: Preclinical
Molecular Formula: C22H28N2O5
Molecular Weight: 400.48
Associated Items:
Names and Identifiers Canonical SMILES: O=[N+]([O-])c1ccccc1COc1ccc(OCCOCCNC2CCCC2)cc1
Standard InChI: InChI=1S/C22H28N2O5/c25-24(26)22-8-4-1-5-18(22)17-29-21-11-9-20(10-12-21)28-16-15-27-14-13-23-19-6-2-3-7-19/h1,4-5,8-12,19,23H,2-3,6-7,13-17H2
Standard InChI Key: VMCSZTPHYAGQAY-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: 400.48Molecular Weight (Monoisotopic): 400.1998AlogP: 4.10#Rotatable Bonds: 12Polar Surface Area: 82.86Molecular Species: BASEHBA: 6HBD: 1#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 4.27CX LogD: 1.73Aromatic Rings: 2Heavy Atoms: 29QED Weighted: 0.33Np Likeness Score: -1.08
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 ]