ID: ALA2271085

Max Phase: Preclinical

Molecular Formula: C15H16N6O6S2

Molecular Weight: 440.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2c([S+](C)[O-])nc3ccccn23)n1

Standard InChI:  InChI=1S/C15H16N6O6S2/c1-26-10-8-11(27-2)18-14(17-10)19-15(22)20-29(24,25)13-12(28(3)23)16-9-6-4-5-7-21(9)13/h4-8H,1-3H3,(H2,17,18,19,20,22)

Standard InChI Key:  ALAPSEISJNALDJ-UHFFFAOYSA-N

Associated Targets(non-human)

Chenopodium album 769 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Stellaria media 151 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sinapis arvensis 41 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Matricaria chamomilla 44 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bromus tectorum 40 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alopecurus myosuroides 149 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Avena fatua 609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Triticum aestivum 1582 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: 440.46Molecular Weight (Monoisotopic): 440.0573AlogP: 0.39#Rotatable Bonds: 6
Polar Surface Area: 159.87Molecular Species: ACIDHBA: 10HBD: 2
#RO5 Violations: 0HBA (Lipinski): 12HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 5.04CX Basic pKa: 2.68CX LogP: 0.31CX LogD: -0.62
Aromatic Rings: 3Heavy Atoms: 29QED Weighted: 0.52Np Likeness Score: -1.40

References

1. ITOH S, OHTA K, YAMAWAKI T, ISHIDA Y.  (2001)  Synthesis and Herbicidal Activity of Sulfonylurea Compounds with Imidazo [1, 2-a] pyridine Moiety,  26  (2): [10.1584/jpestics.26.162]

Source