ID: ALA2228891

Max Phase: Preclinical

Molecular Formula: C16H15N3O2

Molecular Weight: 281.32

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCOC(=O)c1cccc2nc3c(N)cccc3nc12

Standard InChI:  InChI=1S/C16H15N3O2/c1-2-9-21-16(20)10-5-3-7-12-14(10)18-13-8-4-6-11(17)15(13)19-12/h3-8H,2,9,17H2,1H3

Standard InChI Key:  OEBNEJGWJYJAOI-UHFFFAOYSA-N

Associated Targets(non-human)

Botryosphaeria berengeriana 484 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium graminearum 1554 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium oxysporum 3998 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycosphaerella arachidis 441 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria solani 773 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: 281.32Molecular Weight (Monoisotopic): 281.1164AlogP: 2.93#Rotatable Bonds: 3
Polar Surface Area: 78.10Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 2.43CX LogP: 3.11CX LogD: 3.11
Aromatic Rings: 3Heavy Atoms: 21QED Weighted: 0.45Np Likeness Score: -0.35

References

1. Wang MZ, Xu H, Yu SJ, Feng Q, Wang SH, Li ZM..  (2010)  Synthesis and fungicidal activity of novel aminophenazine-1-carboxylate derivatives.,  58  (6): [PMID:20166721] [10.1021/jf904408c]

Source