ID: ALA3741920

Max Phase: Preclinical

Molecular Formula: C13H8O5S

Molecular Weight: 276.27

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=c1cc(-c2cccs2)oc2cc(O)c(O)c(O)c12

Standard InChI:  InChI=1S/C13H8O5S/c14-6-4-8(10-2-1-3-19-10)18-9-5-7(15)12(16)13(17)11(6)9/h1-5,15-17H

Standard InChI Key:  ULDFHXZTKRIFLY-UHFFFAOYSA-N

Associated Targets(Human)

Receptor-type tyrosine-protein phosphatase S 105 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: 276.27Molecular Weight (Monoisotopic): 276.0092AlogP: 2.64#Rotatable Bonds: 1
Polar Surface Area: 90.90Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.75CX Basic pKa: CX LogP: 2.62CX LogD: 1.86
Aromatic Rings: 3Heavy Atoms: 19QED Weighted: 0.59Np Likeness Score: 0.56

References

1. Lee HS, Ku B, Park TH, Park H, Choi JK, Chang KT, Kim CH, Ryu SE, Kim SJ..  (2016)  Identification of novel protein tyrosine phosphatase sigma inhibitors promoting neurite extension.,  26  (1): [PMID:26602279] [10.1016/j.bmcl.2015.11.026]

Source