3-phenyl-1H-isochromene-1-thione

ID: ALA2295876

Chembl Id: CHEMBL2295876

PubChem CID: 12554197

Max Phase: Preclinical

Molecular Formula: C15H10OS

Molecular Weight: 238.31

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  S=c1oc(-c2ccccc2)cc2ccccc12

Standard InChI:  InChI=1S/C15H10OS/c17-15-13-9-5-4-8-12(13)10-14(16-15)11-6-2-1-3-7-11/h1-10H

Standard InChI Key:  UVKOESWGUWOEDO-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

Associated Targets(non-human)

LPO Lactoperoxidase (91 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Calculated Properties

Molecular Weight: 238.31Molecular Weight (Monoisotopic): 238.0452AlogP: 4.83#Rotatable Bonds: 1
Polar Surface Area: 13.14Molecular Species: HBA: 2HBD: 0
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.24CX LogD: 4.24
Aromatic Rings: 3Heavy Atoms: 17QED Weighted: 0.56Np Likeness Score: -0.11

References

1. Kirthana MV, Nawaz Khan F, Sivakumar PM, Doble M, Manivel P, Prabakaran K, Krishnakumar V.  (2013)  Antithyroid agents and QSAR studies: inhibition of lactoperoxidase-catalyzed iodination reaction by isochromene-1-thiones,  22  (10): [10.1007/s00044-013-0475-x]

Source