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N,N-Diethyl-2-{[8-methoxy-2-(4-propoxyphenyl)quinolin-4-yl]-oxy}ethanamine ID: ALA4164881
Chembl Id: CHEMBL4164881
PubChem CID: 145960310
Max Phase: Preclinical
Molecular Formula: C25H32N2O3
Molecular Weight: 408.54
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCCOc1ccc(-c2cc(OCCN(CC)CC)c3cccc(OC)c3n2)cc1
Standard InChI: InChI=1S/C25H32N2O3/c1-5-16-29-20-13-11-19(12-14-20)22-18-24(30-17-15-27(6-2)7-3)21-9-8-10-23(28-4)25(21)26-22/h8-14,18H,5-7,15-17H2,1-4H3
Standard InChI Key: JXCAZCGMXHCFIR-UHFFFAOYSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: 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: 408.54Molecular Weight (Monoisotopic): 408.2413AlogP: 5.42#Rotatable Bonds: 11Polar Surface Area: 43.82Molecular Species: BASEHBA: 5HBD: ┄#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): ┄#RO5 Violations (Lipinski): 1CX Acidic pKa: ┄CX Basic pKa: 9.28CX LogP: 5.30CX LogD: 3.42Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.42Np Likeness Score: -1.03
References 1. Felicetti T, Cannalire R, Pietrella D, Latacz G, Lubelska A, Manfroni G, Barreca ML, Massari S, Tabarrini O, Kieć-Kononowicz K, Schindler BD, Kaatz GW, Cecchetti V, Sabatini S.. (2018) 2-Phenylquinoline S. aureus NorA Efflux Pump Inhibitors: Evaluation of the Importance of Methoxy Group Introduction., 61 (17): [PMID:30067360 ] [10.1021/acs.jmedchem.8b00791 ] 2. Nizi MG, Persoons L, Corona A, Felicetti T, Cernicchi G, Massari S, Manfroni G, Vangeel L, Barreca ML, Esposito F, Jochmans D, Milia J, Cecchetti V, Schols D, Neyts J, Tramontano E, Sabatini S, De Jonghe S, Tabarrini O.. (2022) Discovery of 2-Phenylquinolines with Broad-Spectrum Anti-coronavirus Activity., 13 (5.0): [PMID:35571875 ] [10.1021/acsmedchemlett.2c00123 ]