ID: ALA2238308

Max Phase: Preclinical

Molecular Formula: C16H30N2O3

Molecular Weight: 298.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1/C(=N\O)CC(C(C)(C)C)NC1C(C)(C)C

Standard InChI:  InChI=1S/C16H30N2O3/c1-8-21-14(19)12-10(18-20)9-11(15(2,3)4)17-13(12)16(5,6)7/h11-13,17,20H,8-9H2,1-7H3/b18-10-

Standard InChI Key:  FJMLCEYZQYOTSE-ZDLGFXPLSA-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: 298.43Molecular Weight (Monoisotopic): 298.2256AlogP: 2.82#Rotatable Bonds: 2
Polar Surface Area: 70.92Molecular Species: BASEHBA: 5HBD: 2
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 11.11CX Basic pKa: 9.12CX LogP: 3.29CX LogD: 1.66
Aromatic Rings: 0Heavy Atoms: 21QED Weighted: 0.47Np Likeness Score: 0.02

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