ID: ALA4788628

Max Phase: Preclinical

Molecular Formula: C29H24FN5O4S

Molecular Weight: 557.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ncc([N+](=O)[O-])n1CCOc1ccc(/C=C2\S/C(=N\c3ccccc3)N(Cc3ccc(F)cc3)C2=O)cc1

Standard InChI:  InChI=1S/C29H24FN5O4S/c1-20-31-18-27(35(37)38)33(20)15-16-39-25-13-9-21(10-14-25)17-26-28(36)34(19-22-7-11-23(30)12-8-22)29(40-26)32-24-5-3-2-4-6-24/h2-14,17-18H,15-16,19H2,1H3/b26-17-,32-29-

Standard InChI Key:  UJSZOYJJEIFISL-YJOBWLRUSA-N

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: 557.61Molecular Weight (Monoisotopic): 557.1533AlogP: 6.12#Rotatable Bonds: 9
Polar Surface Area: 102.86Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 3.45CX LogP: 5.90CX LogD: 5.90
Aromatic Rings: 4Heavy Atoms: 40QED Weighted: 0.14Np Likeness Score: -1.89

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