ID: ALA2271977

Max Phase: Preclinical

Molecular Formula: C17H13NO3

Molecular Weight: 279.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(O)Cc1cn(C(=O)c2ccccc2)c2ccccc12

Standard InChI:  InChI=1S/C17H13NO3/c19-16(20)10-13-11-18(15-9-5-4-8-14(13)15)17(21)12-6-2-1-3-7-12/h1-9,11H,10H2,(H,19,20)

Standard InChI Key:  WJZAUHSWEJWXPU-UHFFFAOYSA-N

Associated Targets(non-human)

Macrophomina phaseolina 474 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhizoctonia solani 2251 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Globisporangium debaryanum 107 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium culmorum 260 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 279.30Molecular Weight (Monoisotopic): 279.0895AlogP: 2.96#Rotatable Bonds: 3
Polar Surface Area: 59.30Molecular Species: ACIDHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 4.01CX Basic pKa: CX LogP: 2.88CX LogD: -0.27
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.80Np Likeness Score: -0.63

References

1. Abdel-Aty AS.  (2010)  Fungicidal activity of indole derivatives against some plant pathogenic fungi,  35  (4): [10.1584/jpestics.G09-66]

Source