3-methyl-3-phenyl-9-(propylsulfonyl)-1,2,4,5-tetraoxa-9-azaspiro[5.5]undecane

ID: ALA5269630

Chembl Id: CHEMBL5269630

Max Phase: Preclinical

Molecular Formula: C16H23NO6S

Molecular Weight: 357.43

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCS(=O)(=O)N1CCC2(CC1)OOC(C)(c1ccccc1)OO2

Standard InChI:  InChI=1S/C16H23NO6S/c1-3-13-24(18,19)17-11-9-16(10-12-17)22-20-15(2,21-23-16)14-7-5-4-6-8-14/h4-8H,3,9-13H2,1-2H3

Standard InChI Key:  JBXDKFSYARDXAX-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5269630

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Associated Targets(Human)

Huh-7 (12904 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 357.43Molecular Weight (Monoisotopic): 357.1246AlogP: 2.30#Rotatable Bonds: 4
Polar Surface Area: 74.30Molecular Species: HBA: 6HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.27CX LogD: 3.27
Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.77Np Likeness Score: -0.58

References

1. Singh P, Sharma C, Sharma B, Mishra A, Agarwal D, Kannan D, Held J, Singh S, Awasthi SK..  (2022)  N-sulfonylpiperidinedispiro-1,2,4,5-tetraoxanes exhibit potent in vitro antiplasmodial activity and in vivo efficacy in mice infected with P. berghei ANKA.,  244  [PMID:36306538] [10.1016/j.ejmech.2022.114774]

Source