ID: ALA2287566

Max Phase: Preclinical

Molecular Formula: C17H16N2O3

Molecular Weight: 296.33

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)c1ccc(OCc2nc3ccccc3n2C)cc1

Standard InChI:  InChI=1S/C17H16N2O3/c1-19-15-6-4-3-5-14(15)18-16(19)11-22-13-9-7-12(8-10-13)17(20)21-2/h3-10H,11H2,1-2H3

Standard InChI Key:  QUQSEFPMHWPIRI-UHFFFAOYSA-N

Associated Targets(non-human)

Fusarium solani 1274 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alternaria solani 773 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botrytis cinerea 4183 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Colletotrichum gloeosporioides 560 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytospora 178 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: 296.33Molecular Weight (Monoisotopic): 296.1161AlogP: 2.94#Rotatable Bonds: 4
Polar Surface Area: 53.35Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.38CX LogP: 3.13CX LogD: 3.13
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.69Np Likeness Score: -1.33

References

1. Bai YB, Zhang AL, Tang JJ, Gao JM..  (2013)  Synthesis and antifungal activity of 2-chloromethyl-1H-benzimidazole derivatives against phytopathogenic fungi in vitro.,  61  (11): [PMID:23419161] [10.1021/jf3053934]

Source