ID: ALA2238313

Max Phase: Preclinical

Molecular Formula: C14H26N2O2

Molecular Weight: 254.37

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1C(=O)CC(C(C)(C)C)N(N=O)C1C(C)(C)C

Standard InChI:  InChI=1S/C14H26N2O2/c1-9-10(17)8-11(13(2,3)4)16(15-18)12(9)14(5,6)7/h9,11-12H,8H2,1-7H3

Standard InChI Key:  WTXUXFBVNRFVME-UHFFFAOYSA-N

Associated Targets(non-human)

Trichoderma 92 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Aspergillus niger 16508 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Klebsiella pneumoniae 43867 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Escherichia coli 133304 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bacillus subtilis 32866 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

Properties

Molecular Weight: 254.37Molecular Weight (Monoisotopic): 254.1994AlogP: 3.41#Rotatable Bonds: 1
Polar Surface Area: 49.74Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.01CX LogP: 3.93CX LogD: 3.93
Aromatic Rings: 0Heavy Atoms: 18QED Weighted: 0.67Np Likeness Score: 0.32

References

1. Govindaraju C, Valliappan R, Sundari V.  (2012)  Synthesis and antimicrobial screening of novel 2,6-ditertiarybutylpiperidin-4-ones,  21  (11): [10.1007/s00044-011-9913-9]

Source