ID: ALA4750119

Max Phase: Preclinical

Molecular Formula: C28H24N6O4S

Molecular Weight: 540.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ncc([N+](=O)[O-])n1CCOc1ccc(/C=C2\S/C(=N\c3ccccc3)N(Cc3ccncc3)C2=O)cc1

Standard InChI:  InChI=1S/C28H24N6O4S/c1-20-30-18-26(34(36)37)32(20)15-16-38-24-9-7-21(8-10-24)17-25-27(35)33(19-22-11-13-29-14-12-22)28(39-25)31-23-5-3-2-4-6-23/h2-14,17-18H,15-16,19H2,1H3/b25-17-,31-28-

Standard InChI Key:  KLCTUAJHOZWARG-VHJVTWIDSA-N

Associated Targets(Human)

HEK293 82097 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Entamoeba histolytica 2676 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: 540.61Molecular Weight (Monoisotopic): 540.1580AlogP: 5.38#Rotatable Bonds: 9
Polar Surface Area: 115.75Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 2HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 5.03CX LogP: 4.54CX LogD: 4.54
Aromatic Rings: 4Heavy Atoms: 39QED Weighted: 0.16Np Likeness Score: -1.79

References

1. Ansari MF,Inam A,Ahmad K,Fatima S,Agarwal SM,Azam A.  (2020)  Synthesis of metronidazole based thiazolidinone analogs as promising antiamoebic agents.,  30  (23): [PMID:32927029] [10.1016/j.bmcl.2020.127549]

Source