ID: ALA4848217

Max Phase: Preclinical

Molecular Formula: C19H21N3OS

Molecular Weight: 339.46

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCC1CCNCC1)c1cc2ccc(-c3ccsc3)cc2[nH]1

Standard InChI:  InChI=1S/C19H21N3OS/c23-19(21-11-13-3-6-20-7-4-13)18-10-15-2-1-14(9-17(15)22-18)16-5-8-24-12-16/h1-2,5,8-10,12-13,20,22H,3-4,6-7,11H2,(H,21,23)

Standard InChI Key:  UKQZWVLJWBJNRF-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: 339.46Molecular Weight (Monoisotopic): 339.1405AlogP: 3.63#Rotatable Bonds: 4
Polar Surface Area: 56.92Molecular Species: BASEHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.05CX LogP: 2.60CX LogD: 0.04
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.68Np Likeness Score: -1.31

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