ID: ALA5199339

Max Phase: Preclinical

Molecular Formula: C17H10F3N3O2S

Molecular Weight: 377.35

Associated Items:

Representations

Canonical SMILES:  FC(F)(F)c1cccc(-c2nc(Cc3cc(-c4cccs4)no3)no2)c1

Standard InChI:  InChI=1S/C17H10F3N3O2S/c18-17(19,20)11-4-1-3-10(7-11)16-21-15(23-25-16)9-12-8-13(22-24-12)14-5-2-6-26-14/h1-8H,9H2

Standard InChI Key:  NXKNQKUUTUIDTD-UHFFFAOYSA-N

Associated Targets(Human)

TZM 838 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Human immunodeficiency virus 1 70413 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: 377.35Molecular Weight (Monoisotopic): 377.0446AlogP: 5.06#Rotatable Bonds: 4
Polar Surface Area: 64.95Molecular Species: NEUTRALHBA: 6HBD: 0
#RO5 Violations: 1HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 5.06CX LogD: 5.06
Aromatic Rings: 4Heavy Atoms: 26QED Weighted: 0.50Np Likeness Score: -2.20

References

1. Kumar Kushwaha P, Saurabh Srivastava K, Kumari N, Kumar R, Mitra D, Sharon A..  (2022)  Synthesis and anti-HIV activity of a new isoxazole containing disubstituted 1,2,4-oxadiazoles analogs.,  56  [PMID:35026631] [10.1016/j.bmc.2022.116612]

Source