ID: ALA4784402

Max Phase: Preclinical

Molecular Formula: C21H17N3O3

Molecular Weight: 359.39

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCN1C(=O)C2(OCC=C2c2nc(-c3ccccc3)no2)c2ccccc21

Standard InChI:  InChI=1S/C21H17N3O3/c1-2-24-17-11-7-6-10-15(17)21(20(24)25)16(12-13-26-21)19-22-18(23-27-19)14-8-4-3-5-9-14/h3-12H,2,13H2,1H3

Standard InChI Key:  FTZDQMKQKBYQLN-UHFFFAOYSA-N

Associated Targets(Human)

HFF-1 186 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HepG2 196354 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Trypanosoma cruzi 99888 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Leishmania infantum 5912 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: 359.39Molecular Weight (Monoisotopic): 359.1270AlogP: 3.41#Rotatable Bonds: 3
Polar Surface Area: 68.46Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.72CX LogD: 3.72
Aromatic Rings: 3Heavy Atoms: 27QED Weighted: 0.72Np Likeness Score: -0.69

References

1. Fernandes FS,Santos H,Lima SR,Conti C,Rodrigues MT,Zeoly LA,Ferreira LLG,Krogh R,Andricopulo AD,Coelho F.  (2020)  Discovery of highly potent and selective antiparasitic new oxadiazole and hydroxy-oxindole small molecule hybrids.,  201  [PMID:32590115] [10.1016/j.ejmech.2020.112418]

Source