ID: ALA2011706

Max Phase: Preclinical

Molecular Formula: C32H26N2O5S

Molecular Weight: 550.64

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccc(/N=C2\S/C(=C\c3ccc(OCc4ccccc4)cc3)C(=O)N2Cc2ccc(C(=O)O)cc2)cc1

Standard InChI:  InChI=1S/C32H26N2O5S/c1-38-27-17-13-26(14-18-27)33-32-34(20-23-7-11-25(12-8-23)31(36)37)30(35)29(40-32)19-22-9-15-28(16-10-22)39-21-24-5-3-2-4-6-24/h2-19H,20-21H2,1H3,(H,36,37)/b29-19-,33-32-

Standard InChI Key:  YSDFKOUUBRUKRX-PCYGFIDKSA-N

Associated Targets(Human)

T-cell protein-tyrosine phosphatase 1317 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Low molecular weight phosphotyrosine protein phosphatase 1161 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein-tyrosine phosphatase 1B 8528 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

C2C12 756 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Protein-tyrosine phosphatase 1B 163 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: 550.64Molecular Weight (Monoisotopic): 550.1562AlogP: 6.78#Rotatable Bonds: 9
Polar Surface Area: 88.43Molecular Species: ACIDHBA: 6HBD: 1
#RO5 Violations: 2HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 4.23CX Basic pKa: 3.55CX LogP: 6.50CX LogD: 3.82
Aromatic Rings: 4Heavy Atoms: 40QED Weighted: 0.23Np Likeness Score: -1.11

References

1. Ottanà R, Maccari R, Amuso S, Wolber G, Schuster D, Herdlinger S, Manao G, Camici G, Paoli P..  (2012)  New 4-[(5-arylidene-2-arylimino-4-oxo-3-thiazolidinyl)methyl]benzoic acids active as protein tyrosine phosphatase inhibitors endowed with insulinomimetic effect on mouse C2C12 skeletal muscle cells.,  50  [PMID:22381357] [10.1016/j.ejmech.2012.02.012]

Source