ID: ALA469530

Max Phase: Preclinical

Molecular Formula: C7H10N2O2S

Molecular Weight: 186.24

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCn1ccn(C(=O)OC)c1=S

Standard InChI:  InChI=1S/C7H10N2O2S/c1-3-8-4-5-9(6(8)12)7(10)11-2/h4-5H,3H2,1-2H3

Standard InChI Key:  BMYOMURFAIAFAL-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: 186.24Molecular Weight (Monoisotopic): 186.0463AlogP: 1.65#Rotatable Bonds: 1
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: 1.35CX LogD: 1.35
Aromatic Rings: 1Heavy Atoms: 12QED Weighted: 0.63Np Likeness Score: -1.15

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