SID87457357

ID: ALA1472977

Chembl Id: CHEMBL1472977

PubChem CID: 44607957

Max Phase: Preclinical

Molecular Formula: C14H15NO6S3

Molecular Weight: 389.48

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CS(=O)(=O)C(=Cc1cccn1S(=O)(=O)c1ccccc1)S(C)(=O)=O

Standard InChI:  InChI=1S/C14H15NO6S3/c1-22(16,17)14(23(2,18)19)11-12-7-6-10-15(12)24(20,21)13-8-4-3-5-9-13/h3-11H,1-2H3

Standard InChI Key:  MOPKWLQQCAXWCB-UHFFFAOYSA-N

Associated Targets(Human)

PPME1 Tchem Protein phosphatase methylesterase 1 (52 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Prep Prolyl endopeptidase (55 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ppme1 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

Calculated Properties

Molecular Weight: 389.48Molecular Weight (Monoisotopic): 389.0062AlogP: 1.11#Rotatable Bonds: 5
Polar Surface Area: 107.35Molecular Species: HBA: 7HBD:
#RO5 Violations: HBA (Lipinski): 7HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 0.61CX LogD: 0.61
Aromatic Rings: 2Heavy Atoms: 24QED Weighted: 0.76Np Likeness Score: -1.00

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]