ID: ALA4754502

Max Phase: Preclinical

Molecular Formula: C27H27N5O5S

Molecular Weight: 533.61

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ncc([N+](=O)[O-])n1CCOc1ccc(/C=C2\S/C(=N\c3ccccc3)N(CC3CCCO3)C2=O)cc1

Standard InChI:  InChI=1S/C27H27N5O5S/c1-19-28-17-25(32(34)35)30(19)13-15-37-22-11-9-20(10-12-22)16-24-26(33)31(18-23-8-5-14-36-23)27(38-24)29-21-6-3-2-4-7-21/h2-4,6-7,9-12,16-17,23H,5,8,13-15,18H2,1H3/b24-16-,29-27-

Standard InChI Key:  LQUNDJIPEJCMMQ-HVSIYQNKSA-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: 533.61Molecular Weight (Monoisotopic): 533.1733AlogP: 4.96#Rotatable Bonds: 9
Polar Surface Area: 112.09Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 3.41CX LogP: 4.46CX LogD: 4.46
Aromatic Rings: 3Heavy Atoms: 38QED Weighted: 0.22Np Likeness Score: -1.64

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