ID: ALA4799745

Max Phase: Preclinical

Molecular Formula: C22H13F8N3O

Molecular Weight: 487.35

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCc1nc2cnc(-c3ccc(F)c(C(F)(F)C(F)(F)F)c3)cn2c1-c1c(F)cc(O)cc1F

Standard InChI:  InChI=1S/C22H13F8N3O/c1-2-16-20(19-14(24)6-11(34)7-15(19)25)33-9-17(31-8-18(33)32-16)10-3-4-13(23)12(5-10)21(26,27)22(28,29)30/h3-9,34H,2H2,1H3

Standard InChI Key:  VANXMDJMYZPYSP-UHFFFAOYSA-N

Associated Targets(Human)

HepG2 196354 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Schistosoma mansoni 6170 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: 487.35Molecular Weight (Monoisotopic): 487.0931AlogP: 6.40#Rotatable Bonds: 4
Polar Surface Area: 50.42Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.93CX Basic pKa: 2.36CX LogP: 5.68CX LogD: 5.57
Aromatic Rings: 4Heavy Atoms: 34QED Weighted: 0.34Np Likeness Score: -0.76

References

1. J. Mark F. Gardner, Nuha R. Mansour, Andrew S. Bell, Helena Helmby, Quentin Bickle.  (2021)  The discovery of a novel series of compounds with single-dose efficacy against juvenile and adult Schistosoma species,  [PMID:34280206] [10.1371/journal.pntd.0009490 ]