tert-Butyl 2-(4-Morpholino-1,2,5-thiadiazol-3-yl)acetate

ID: ALA1082840

Chembl Id: CHEMBL1082840

PubChem CID: 46867141

Max Phase: Preclinical

Molecular Formula: C12H19N3O3S

Molecular Weight: 285.37

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)(C)OC(=O)Cc1nsnc1N1CCOCC1

Standard InChI:  InChI=1S/C12H19N3O3S/c1-12(2,3)18-10(16)8-9-11(14-19-13-9)15-4-6-17-7-5-15/h4-8H2,1-3H3

Standard InChI Key:  XGNKVHFULKFLQR-UHFFFAOYSA-N

Associated Targets(Human)

LIPA Tchem Lysosomal acid lipase/cholesteryl ester hydrolase (63 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: 285.37Molecular Weight (Monoisotopic): 285.1147AlogP: 1.26#Rotatable Bonds: 3
Polar Surface Area: 64.55Molecular Species: NEUTRALHBA: 7HBD:
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: 0.60CX LogP: 2.06CX LogD: 2.06
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.78Np Likeness Score: -1.59

References

1. Rosenbaum AI, Cosner CC, Mariani CJ, Maxfield FR, Wiest O, Helquist P..  (2010)  Thiadiazole carbamates: potent inhibitors of lysosomal acid lipase and potential Niemann-Pick type C disease therapeutics.,  53  (14): [PMID:20557099] [10.1021/jm100499s]

Source