ID: ALA4856855

Max Phase: Preclinical

Molecular Formula: C26H32N4O

Molecular Weight: 416.57

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCC1CCNCC1)c1cc2ccc(-c3ccc(N4CCCCC4)cc3)cc2[nH]1

Standard InChI:  InChI=1S/C26H32N4O/c31-26(28-18-19-10-12-27-13-11-19)25-17-22-5-4-21(16-24(22)29-25)20-6-8-23(9-7-20)30-14-2-1-3-15-30/h4-9,16-17,19,27,29H,1-3,10-15,18H2,(H,28,31)

Standard InChI Key:  GYAFIGZGBJEFEB-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: 416.57Molecular Weight (Monoisotopic): 416.2576AlogP: 4.55#Rotatable Bonds: 5
Polar Surface Area: 60.16Molecular Species: BASEHBA: 3HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 10.05CX LogP: 3.78CX LogD: 1.22
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.57Np Likeness Score: -0.91

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