ID: ALA1718102

Max Phase: Preclinical

Molecular Formula: C19H13FN2O4S2

Molecular Weight: 416.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  N#C/C(=C\c1cccn1S(=O)(=O)c1ccccc1)S(=O)(=O)c1ccc(F)cc1

Standard InChI:  InChI=1S/C19H13FN2O4S2/c20-15-8-10-17(11-9-15)27(23,24)19(14-21)13-16-5-4-12-22(16)28(25,26)18-6-2-1-3-7-18/h1-13H/b19-13+

Standard InChI Key:  NUVDRZPNHCKDBZ-CPNJWEJPSA-N

Associated Targets(Human)

Protein phosphatase methylesterase 1 52 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acylamino-acid-releasing enzyme 14 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Protein phosphatase methylesterase 1 22 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: 416.46Molecular Weight (Monoisotopic): 416.0301AlogP: 3.20#Rotatable Bonds: 5
Polar Surface Area: 97.00Molecular Species: HBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.17CX LogD: 3.17
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.47Np Likeness Score: -1.60

References

1. PubChem BioAssay data set, 
2. Bachovchin DA, Zuhl AM, Speers AE, Wolfe MR, Weerapana E, Brown SJ, Rosen H, Cravatt BF..  (2011)  Discovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1.,  54  (14): [PMID:21639134] [10.1021/jm200502u]