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Ethylene glycol (2-(5,6,7,8-tetrahydronaphthyl)) cyclopentylaminoethyl ether ID: ALA5273841
Chembl Id: CHEMBL5273841
Max Phase: Preclinical
Molecular Formula: C19H29NO2
Molecular Weight: 303.45
Associated Items:
Names and Identifiers Canonical SMILES: c1cc2c(cc1OCCOCCNC1CCCC1)CCCC2
Standard InChI: InChI=1S/C19H29NO2/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/h9-10,15,18,20H,1-8,11-14H2
Standard InChI Key: QIOFIRXSOGLUBW-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: 303.45Molecular Weight (Monoisotopic): 303.2198AlogP: 3.49#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: 4.21CX LogD: 1.68Aromatic Rings: 1Heavy 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 ]