(2-Chloro-4-ethanesulfonyl-3-ethoxy-phenyl)-(3-hydroxy-5-methyl-3H-imidazol-4-yl)-methanone

ID: ALA2251436

Chembl Id: CHEMBL2251436

PubChem CID: 76308247

Max Phase: Preclinical

Molecular Formula: C15H17ClN2O5S

Molecular Weight: 372.83

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCOc1c(S(=O)(=O)CC)ccc(C(=O)c2c(C)ncn2O)c1Cl

Standard InChI:  InChI=1S/C15H17ClN2O5S/c1-4-23-15-11(24(21,22)5-2)7-6-10(12(15)16)14(19)13-9(3)17-8-18(13)20/h6-8,20H,4-5H2,1-3H3

Standard InChI Key:  ZZGALUOTCAIANV-UHFFFAOYSA-N

Associated Targets(non-human)

Chenopodium album (769 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abutilon theophrasti (831 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Echinochloa crus-galli (3685 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPD 4-hydroxyphenylpyruvate dioxygenase (49 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

Calculated Properties

Molecular Weight: 372.83Molecular Weight (Monoisotopic): 372.0547AlogP: 2.51#Rotatable Bonds: 6
Polar Surface Area: 98.49Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 9.78CX Basic pKa: 3.23CX LogP: 0.85CX LogD: 0.84
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.62Np Likeness Score: -0.98

References

1. Witschel M..  (2009)  Design, synthesis and herbicidal activity of new iron chelating motifs for HPPD-inhibitors.,  17  (12): [PMID:19028100] [10.1016/j.bmc.2008.11.006]

Source