ID: ALA4855758

Max Phase: Preclinical

Molecular Formula: C20H22N4O

Molecular Weight: 334.42

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCC1CCNCC1)c1cc2ccc(-c3ccncc3)cc2[nH]1

Standard InChI:  InChI=1S/C20H22N4O/c25-20(23-13-14-3-7-21-8-4-14)19-12-17-2-1-16(11-18(17)24-19)15-5-9-22-10-6-15/h1-2,5-6,9-12,14,21,24H,3-4,7-8,13H2,(H,23,25)

Standard InChI Key:  CFJAZYHCODKCAA-UHFFFAOYSA-N

Associated Targets(non-human)

Genome polyprotein 385 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: 334.42Molecular Weight (Monoisotopic): 334.1794AlogP: 2.96#Rotatable Bonds: 4
Polar Surface Area: 69.81Molecular Species: BASEHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.05CX LogP: 1.60CX LogD: -0.95
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.69Np Likeness Score: -0.77

References

1. Nie S, Zhao J, Wu X, Yao Y, Wu F, Lin YL, Li X, Kneubehl AR, Vogt MB, Rico-Hesse R, Song Y..  (2021)  Synthesis, structure-activity relationship and antiviral activity of indole-containing inhibitors of Flavivirus NS2B-NS3 protease.,  225  [PMID:34450494] [10.1016/j.ejmech.2021.113767]

Source