ID: ALA2287501

Max Phase: Preclinical

Molecular Formula: C17H22N2O4

Molecular Weight: 318.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCc1cc(C)cc(OC)c1C1C(=O)N2CCOCCN2C1=O

Standard InChI:  InChI=1S/C17H22N2O4/c1-4-12-9-11(2)10-13(22-3)14(12)15-16(20)18-5-7-23-8-6-19(18)17(15)21/h9-10,15H,4-8H2,1-3H3

Standard InChI Key:  HAJRDDNBYSVTMU-UHFFFAOYSA-N

Associated Targets(non-human)

Setaria faberi 210 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lolium perenne 157 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Avena fatua 609 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alopecurus myosuroides 149 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Triticum aestivum 1582 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hordeum vulgare 329 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: 318.37Molecular Weight (Monoisotopic): 318.1580AlogP: 1.27#Rotatable Bonds: 3
Polar Surface Area: 59.08Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.55CX Basic pKa: CX LogP: 1.72CX LogD: 0.81
Aromatic Rings: 1Heavy Atoms: 23QED Weighted: 0.79Np Likeness Score: -0.23

References

1. Muehlebach M, Cederbaum F, Cornes D, Friedmann AA, Glock J, Hall G, Indolese AF, Kloer DP, Le Goupil G, Maetzke T, Meier H, Schneider R, Stoller A, Szczepanski H, Wendeborn S, Widmer H..  (2011)  Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part 2: chemistry and biology of the cereal herbicide pinoxaden.,  67  (12): [PMID:21656896] [10.1002/ps.2204]

Source