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

ID: ALA5277060

Chembl Id: CHEMBL5277060

Max Phase: Preclinical

Molecular Formula: C13H25NO6S

Molecular Weight: 323.41

Associated Items:

Names and Identifiers

Canonical SMILES:  CCCC1(C)OOC2(CCN(S(=O)(=O)CCC)CC2)OO1

Standard InChI:  InChI=1S/C13H25NO6S/c1-4-6-12(3)17-19-13(20-18-12)7-9-14(10-8-13)21(15,16)11-5-2/h4-11H2,1-3H3

Standard InChI Key:  CMPQXVCVRLDTOH-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA5277060

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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
Plasmodium berghei (192651 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: 323.41Molecular Weight (Monoisotopic): 323.1403AlogP: 1.94#Rotatable Bonds: 5
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: 2.64CX LogD: 2.64
Aromatic Rings: 0Heavy Atoms: 21QED Weighted: 0.72Np Likeness Score: -0.55

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