ID: ALA5271323

Max Phase: Preclinical

Molecular Formula: C16H12F3NO2S

Molecular Weight: 339.34

Associated Items:

Representations

Canonical SMILES:  N#CSCCOc1ccc(Oc2ccc(C(F)(F)F)cc2)cc1

Standard InChI:  InChI=1S/C16H12F3NO2S/c17-16(18,19)12-1-3-14(4-2-12)22-15-7-5-13(6-8-15)21-9-10-23-11-20/h1-8H,9-10H2

Standard InChI Key:  HMHWUZBQHQQBGI-UHFFFAOYSA-N

Associated Targets(non-human)

Toxoplasma gondii 4585 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Vero 26788 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 339.34Molecular Weight (Monoisotopic): 339.0541AlogP: 5.09#Rotatable Bonds: 6
Polar Surface Area: 42.25Molecular Species: NEUTRALHBA: 4HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.66CX LogD: 4.66
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.54Np Likeness Score: -1.01

References

1. Wu RZ, Zhou HY, Song JF, Xia QH, Hu W, Mou XD, Li X..  (2021)  Chemotherapeutics for Toxoplasma gondii: Molecular Biotargets, Binding Modes, and Structure-Activity Relationship Investigations.,  64  (24.0): [PMID:34894691] [10.1021/acs.jmedchem.1c01569]

Source