ID: ALA469529

Max Phase: Preclinical

Molecular Formula: C8H12N2O2S

Molecular Weight: 200.26

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)n1ccn(CC)c1=S

Standard InChI:  InChI=1S/C8H12N2O2S/c1-3-9-5-6-10(7(9)13)8(11)12-4-2/h5-6H,3-4H2,1-2H3

Standard InChI Key:  LFATYVGOCRFYMS-UHFFFAOYSA-N

Associated Targets(Human)

Lactoperoxidase 15 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

Properties

Molecular Weight: 200.26Molecular Weight (Monoisotopic): 200.0619AlogP: 2.04#Rotatable Bonds: 2
Polar Surface Area: 36.16Molecular Species: HBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.71CX LogD: 1.71
Aromatic Rings: 1Heavy Atoms: 13QED Weighted: 0.69Np Likeness Score: -1.30

References

1. Das D, Roy G, Mugesh G..  (2008)  Antithyroid drug carbimazole and its analogues: synthesis and inhibition of peroxidase-catalyzed iodination of L-tyrosine.,  51  (22): [PMID:18954039] [10.1021/jm800894m]

Source