ID: ALA4641525

Max Phase: Preclinical

Molecular Formula: C16H13NO3

Molecular Weight: 267.28

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  O=C(O)C(=O)Nc1ccc(/C=C\c2ccccc2)cc1

Standard InChI:  InChI=1S/C16H13NO3/c18-15(16(19)20)17-14-10-8-13(9-11-14)7-6-12-4-2-1-3-5-12/h1-11H,(H,17,18)(H,19,20)/b7-6-

Standard InChI Key:  OTGXVFHPSDRWPP-SREVYHEPSA-N

Associated Targets(Human)

Protein-tyrosine phosphatase 2C 2297 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)

Phosphotyrosine protein phosphatase 409 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: 267.28Molecular Weight (Monoisotopic): 267.0895AlogP: 2.88#Rotatable Bonds: 3
Polar Surface Area: 66.40Molecular Species: ACIDHBA: 2HBD: 2
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 2.71CX Basic pKa: CX LogP: 3.51CX LogD: 0.01
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.66Np Likeness Score: -0.41

References

1. Ruddraraju KV, Aggarwal D, Niu C, Baker EA, Zhang RY, Wu L, Zhang ZY..  (2020)  Highly Potent and Selective N-Aryl Oxamic Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B.,  63  (17): [PMID:32787087] [10.1021/acs.jmedchem.0c00302]

Source