ID: ALA4855322

Max Phase: Preclinical

Molecular Formula: C18H18N2O3

Molecular Weight: 310.35

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NC1CCNCC1)c1coc2cc(-c3ccoc3)ccc12

Standard InChI:  InChI=1S/C18H18N2O3/c21-18(20-14-3-6-19-7-4-14)16-11-23-17-9-12(1-2-15(16)17)13-5-8-22-10-13/h1-2,5,8-11,14,19H,3-4,6-7H2,(H,20,21)

Standard InChI Key:  SFHBHNRUFXCLQT-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: 310.35Molecular Weight (Monoisotopic): 310.1317AlogP: 3.17#Rotatable Bonds: 3
Polar Surface Area: 67.41Molecular Species: BASEHBA: 4HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.03CX LogP: 1.64CX LogD: -0.90
Aromatic Rings: 3Heavy Atoms: 23QED Weighted: 0.78Np Likeness Score: -0.19

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