ID: ALA4861673

Max Phase: Preclinical

Molecular Formula: C17H18N2O5

Molecular Weight: 330.34

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CCOc1ccc(C(=O)NO)cc1NC(=O)c1ccc(OC)cc1

Standard InChI:  InChI=1S/C17H18N2O5/c1-3-24-15-9-6-12(17(21)19-22)10-14(15)18-16(20)11-4-7-13(23-2)8-5-11/h4-10,22H,3H2,1-2H3,(H,18,20)(H,19,21)

Standard InChI Key:  KJYQSZPZKJBTGR-UHFFFAOYSA-N

Associated Targets(Human)

HEK293 82097 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Histone deacetylase 8 483 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Schistosoma mansoni 6170 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 330.34Molecular Weight (Monoisotopic): 330.1216AlogP: 2.47#Rotatable Bonds: 6
Polar Surface Area: 96.89Molecular Species: NEUTRALHBA: 5HBD: 3
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 9.20CX Basic pKa: CX LogP: 1.95CX LogD: 1.95
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.56Np Likeness Score: -1.24

References

1. Ghazy E, Heimburg T, Lancelot J, Zeyen P, Schmidtkunz K, Truhn A, Darwish S, Simoben CV, Shaik TB, Erdmann F, Schmidt M, Robaa D, Romier C, Jung M, Pierce R, Sippl W..  (2021)  Synthesis, structure-activity relationships, cocrystallization and cellular characterization of novel smHDAC8 inhibitors for the treatment of schistosomiasis.,  225  [PMID:34392190] [10.1016/j.ejmech.2021.113745]

Source