2-{[6,8-Dimethoxy-2-(4-propoxyphenyl)quinolin-4-yl]oxy}-N,N-diethylethanamine

ID: ALA4168943

Chembl Id: CHEMBL4168943

PubChem CID: 145952799

Max Phase: Preclinical

Molecular Formula: C26H34N2O4

Molecular Weight: 438.57

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCOc1ccc(-c2cc(OCCN(CC)CC)c3cc(OC)cc(OC)c3n2)cc1

Standard InChI:  InChI=1S/C26H34N2O4/c1-6-14-31-20-11-9-19(10-12-20)23-18-24(32-15-13-28(7-2)8-3)22-16-21(29-4)17-25(30-5)26(22)27-23/h9-12,16-18H,6-8,13-15H2,1-5H3

Standard InChI Key:  DHWIZECKOOPCKX-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA4168943

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Associated Targets(Human)

HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THP-1 (11052 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HEL 299 (144 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

norA Quinolone resistance protein norA (2171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Vero C1008 (1716 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Human coronavirus 229E (235 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 438.57Molecular Weight (Monoisotopic): 438.2519AlogP: 5.43#Rotatable Bonds: 12
Polar Surface Area: 53.05Molecular Species: BASEHBA: 6HBD:
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.30CX LogP: 5.14CX LogD: 3.25
Aromatic Rings: 3Heavy Atoms: 32QED Weighted: 0.38Np Likeness Score: -0.86

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]

Source