ID: ALA2271075

Max Phase: Preclinical

Molecular Formula: C20H18N6O5S2

Molecular Weight: 486.54

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2c(Sc3ccccc3)nc3ccccn23)n1

Standard InChI:  InChI=1S/C20H18N6O5S2/c1-30-15-12-16(31-2)23-19(22-15)24-20(27)25-33(28,29)18-17(32-13-8-4-3-5-9-13)21-14-10-6-7-11-26(14)18/h3-12H,1-2H3,(H2,22,23,24,25,27)

Standard InChI Key:  GZMRRDNZFCDGDL-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: 486.54Molecular Weight (Monoisotopic): 486.0780AlogP: 2.80#Rotatable Bonds: 7
Polar Surface Area: 136.81Molecular Species: ACIDHBA: 10HBD: 2
#RO5 Violations: 0HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 5.05CX Basic pKa: 2.72CX LogP: 3.76CX LogD: 2.83
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.40Np Likeness Score: -1.57

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