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Ethylene glycol (4-(1H-1,2,4-triazolyl)phenyl)cyclopentylaminoethyl ether ID: ALA5268794
Chembl Id: CHEMBL5268794
Max Phase: Preclinical
Molecular Formula: C17H24N4O2
Molecular Weight: 316.40
Associated Items:
Names and Identifiers Canonical SMILES: c1ncn(-c2ccc(OCCOCCNC3CCCC3)cc2)n1
Standard InChI: InChI=1S/C17H24N4O2/c1-2-4-15(3-1)19-9-10-22-11-12-23-17-7-5-16(6-8-17)21-14-18-13-20-21/h5-8,13-15,19H,1-4,9-12H2
Standard InChI Key: GVZVRDGWYJXUBN-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: 316.40Molecular Weight (Monoisotopic): 316.1899AlogP: 2.19#Rotatable Bonds: 9Polar Surface Area: 61.20Molecular Species: BASEHBA: 6HBD: 1#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 2.16CX LogD: -0.38Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.72Np Likeness Score: -1.78
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 ]