ID: ALA2252858

Max Phase: Preclinical

Molecular Formula: C9H6F2N2O3S

Molecular Weight: 260.22

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CS(=O)(=O)c1nnc(-c2c(F)cccc2F)o1

Standard InChI:  InChI=1S/C9H6F2N2O3S/c1-17(14,15)9-13-12-8(16-9)7-5(10)3-2-4-6(7)11/h2-4H,1H3

Standard InChI Key:  XLQQPFQTFGSMFH-UHFFFAOYSA-N

Associated Targets(non-human)

Cytospora 178 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Fusarium oxysporum 3998 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Thanatephorus cucumeris 609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sclerotinia sclerotiorum 877 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Colletotrichum gloeosporioides 560 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Phytophthora infestans 820 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Botrytis cinerea 4183 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhizoctonia solani 2251 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: 260.22Molecular Weight (Monoisotopic): 260.0067AlogP: 1.42#Rotatable Bonds: 2
Polar Surface Area: 73.06Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 0.79CX LogD: 0.79
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.82Np Likeness Score: -1.24

References

1. Xu W, He J, He M, Han F, Chen X, Pan Z, Wang J, Tong M..  (2011)  Synthesis and antifungal activity of novel sulfone derivatives containing 1,3,4-oxadiazole moieties.,  16  (11): [PMID:22045041] [10.3390/molecules16119129]

Source