ID: ALA2288502

Max Phase: Preclinical

Molecular Formula: C20H18F2N6O6S

Molecular Weight: 508.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(OC)nc(NC(=O)NS(=O)(=O)c2ncccc2C(=O)N(C)c2ccc(F)cc2F)n1

Standard InChI:  InChI=1S/C20H18F2N6O6S/c1-28(14-7-6-11(21)9-13(14)22)18(29)12-5-4-8-23-17(12)35(31,32)27-20(30)26-19-24-15(33-2)10-16(25-19)34-3/h4-10H,1-3H3,(H2,24,25,26,27,30)

Standard InChI Key:  GXNALWAWNGYLOE-UHFFFAOYSA-N

Associated Targets(non-human)

Sida spinosa 38 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: 508.46Molecular Weight (Monoisotopic): 508.0977AlogP: 1.95#Rotatable Bonds: 7
Polar Surface Area: 152.71Molecular Species: ACIDHBA: 9HBD: 2
#RO5 Violations: 1HBA (Lipinski): 12HBD (Lipinski): 2#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.98CX Basic pKa: 2.68CX LogP: 2.72CX LogD: 1.79
Aromatic Rings: 3Heavy Atoms: 35QED Weighted: 0.49Np Likeness Score: -1.77

References

1. MURAI S, HAGA T, SAKASHITA N, NAKAMURA Y, HONDA C, HONZAWA S, KIMURA F, TSUJII Y, NISHIYAMA R.  (1995)  Synthesis and Herbicidal Activity of Sulfonylureas; SL-950 and Its Related Compounds,  20  (4): [10.1584/jpestics.20.453]

Source