ID: ALA3360389

Max Phase: Preclinical

Molecular Formula: C18H15Cl2NO4

Molecular Weight: 380.23

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(C(=O)CC2(O)C(=O)N(C)c3c(Cl)ccc(Cl)c32)cc1

Standard InChI:  InChI=1S/C18H15Cl2NO4/c1-21-16-13(20)8-7-12(19)15(16)18(24,17(21)23)9-14(22)10-3-5-11(25-2)6-4-10/h3-8,24H,9H2,1-2H3

Standard InChI Key:  GVQHAGOWUURSAR-UHFFFAOYSA-N

Associated Targets(Human)

Friend leukemia integration 1 transcription factor (Proto-oncogene Fli-1)/RNA-binding protein EWS 19 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: 380.23Molecular Weight (Monoisotopic): 379.0378AlogP: 3.44#Rotatable Bonds: 4
Polar Surface Area: 66.84Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.45CX Basic pKa: CX LogP: 2.82CX LogD: 2.82
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.83Np Likeness Score: -0.31

References

1. Tosso PN, Kong Y, Scher L, Cummins R, Schneider J, Rahim S, Holman KT, Toretsky J, Wang K, Üren A, Brown ML..  (2014)  Synthesis and structure-activity relationship studies of small molecule disruptors of EWS-FLI1 interactions in Ewing's sarcoma.,  57  (24): [PMID:25432018] [10.1021/jm501372p]

Source