ID: ALA5070507

Max Phase: Preclinical

Molecular Formula: C19H20FN3O6S2

Molecular Weight: 469.52

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C1CN(c2c(O)cc3ccc(C4CCN(S(=O)(=O)C5CC5)C4)cc3c2F)S(=O)(=O)N1

Standard InChI:  InChI=1S/C19H20FN3O6S2/c20-18-15-7-11(13-5-6-22(9-13)30(26,27)14-3-4-14)1-2-12(15)8-16(24)19(18)23-10-17(25)21-31(23,28)29/h1-2,7-8,13-14,24H,3-6,9-10H2,(H,21,25)

Standard InChI Key:  AYROLBLQVASEBX-UHFFFAOYSA-N

Associated Targets(Human)

T-cell protein-tyrosine phosphatase 1317 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)

B16-F10 4610 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 469.52Molecular Weight (Monoisotopic): 469.0778AlogP: 1.15#Rotatable Bonds: 4
Polar Surface Area: 124.09Molecular Species: ACIDHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 3.77CX Basic pKa: CX LogP: 0.25CX LogD: -0.75
Aromatic Rings: 2Heavy Atoms: 31QED Weighted: 0.69Np Likeness Score: -0.78

References

1. Abdel-Magid AF..  (2022)  The Inhibitors of Protein Tyrosine Phosphatase Nonreceptor Type 2 (PTPN2) as Potential Enhancers of Cancer Immunotherapy and Type 1 (PTPN1) as Treatment of Metabolic Diseases.,  13  (1.0): [PMID:35059117] [10.1021/acsmedchemlett.1c00678]

Source