2-p-tolyl-4-butyl-1,2,4-thiadiazolidine-3,5-dione

ID: ALA2037362

Chembl Id: CHEMBL2037362

PubChem CID: 70694437

Max Phase: Preclinical

Molecular Formula: C13H16N2O2S

Molecular Weight: 264.35

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCCn1c(=O)sn(-c2ccc(C)cc2)c1=O

Standard InChI:  InChI=1S/C13H16N2O2S/c1-3-4-9-14-12(16)15(18-13(14)17)11-7-5-10(2)6-8-11/h5-8H,3-4,9H2,1-2H3

Standard InChI Key:  YIFYVSULKGSGIO-UHFFFAOYSA-N

Associated Targets(Human)

RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RGS8 Tchem Regulator of G-protein signaling 8 (45 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: 264.35Molecular Weight (Monoisotopic): 264.0932AlogP: 2.17#Rotatable Bonds: 4
Polar Surface Area: 44.00Molecular Species: HBA: 5HBD:
#RO5 Violations: HBA (Lipinski): 4HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: 3.85CX LogD: 3.85
Aromatic Rings: 2Heavy Atoms: 18QED Weighted: 0.85Np Likeness Score: -0.97

References

1. Turner EM, Blazer LL, Neubig RR, Husbands SM..  (2012)  Small Molecule Inhibitors of Regulator of G Protein Signalling (RGS) Proteins.,  (2): [PMID:22368763] [10.1021/ml200263y]

Source