ID: ALA4859564

Max Phase: Preclinical

Molecular Formula: C19H21N5O

Molecular Weight: 335.41

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(NCC1CCNCC1)c1c[nH]c2nc(-c3ccncc3)ccc12

Standard InChI:  InChI=1S/C19H21N5O/c25-19(23-11-13-3-7-20-8-4-13)16-12-22-18-15(16)1-2-17(24-18)14-5-9-21-10-6-14/h1-2,5-6,9-10,12-13,20H,3-4,7-8,11H2,(H,22,24)(H,23,25)

Standard InChI Key:  RQINDWDHLDFVAH-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: 335.41Molecular Weight (Monoisotopic): 335.1746AlogP: 2.35#Rotatable Bonds: 4
Polar Surface Area: 82.70Molecular Species: BASEHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.44CX Basic pKa: 10.05CX LogP: 1.22CX LogD: -1.34
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.68Np Likeness Score: -1.04

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