ID: ALA4522896

Max Phase: Preclinical

Molecular Formula: C20H19N5O3S

Molecular Weight: 409.47

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOCc1cn(-c2cccc(S(=O)(=O)Nc3cccc4cnccc34)c2)nn1

Standard InChI:  InChI=1S/C20H19N5O3S/c1-2-28-14-16-13-25(24-22-16)17-6-4-7-18(11-17)29(26,27)23-20-8-3-5-15-12-21-10-9-19(15)20/h3-13,23H,2,14H2,1H3

Standard InChI Key:  MWQRJWRKRPRWHR-UHFFFAOYSA-N

Associated Targets(Human)

ATP-dependent RNA helicase DDX3X 438 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Huh-7 12904 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

West Nile virus 623 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Properties

Molecular Weight: 409.47Molecular Weight (Monoisotopic): 409.1209AlogP: 3.15#Rotatable Bonds: 7
Polar Surface Area: 99.00Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.46CX Basic pKa: 5.02CX LogP: 2.25CX LogD: 2.02
Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.50Np Likeness Score: -2.17

References

1. Brai A, Martelli F, Riva V, Garbelli A, Fazi R, Zamperini C, Pollutri A, Falsitta L, Ronzini S, Maccari L, Maga G, Giannecchini S, Botta M..  (2019)  DDX3X Helicase Inhibitors as a New Strategy To Fight the West Nile Virus Infection.,  62  (5): [PMID:30721061] [10.1021/acs.jmedchem.8b01403]

Source