ID: ALA2287562

Max Phase: Preclinical

Molecular Formula: C16H14N2O2

Molecular Weight: 266.30

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1c(COc2ccc(C=O)cc2)nc2ccccc21

Standard InChI:  InChI=1S/C16H14N2O2/c1-18-15-5-3-2-4-14(15)17-16(18)11-20-13-8-6-12(10-19)7-9-13/h2-10H,11H2,1H3

Standard InChI Key:  ZTWBBBULVHYDBR-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: 266.30Molecular Weight (Monoisotopic): 266.1055AlogP: 2.96#Rotatable Bonds: 4
Polar Surface Area: 44.12Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 4.38CX LogP: 2.84CX LogD: 2.84
Aromatic Rings: 3Heavy Atoms: 20QED Weighted: 0.68Np Likeness Score: -1.22

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