ID: ALA2228809

Max Phase: Preclinical

Molecular Formula: C24H29NO5

Molecular Weight: 411.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(C)c(C2=C(OC(=O)C(=O)N3CCCCC3)C3(CCCC3)OC2=O)c(C)c1

Standard InChI:  InChI=1S/C24H29NO5/c1-15-13-16(2)18(17(3)14-15)19-20(24(30-22(19)27)9-5-6-10-24)29-23(28)21(26)25-11-7-4-8-12-25/h13-14H,4-12H2,1-3H3

Standard InChI Key:  ISIZMGMXTXVQII-UHFFFAOYSA-N

Associated Targets(non-human)

Tetranychus cinnabarinus 1124 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mythimna separata 3306 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Ostrinia nubilalis 164 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Helicoverpa armigera 708 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: 411.50Molecular Weight (Monoisotopic): 411.2046AlogP: 3.75#Rotatable Bonds: 2
Polar Surface Area: 72.91Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.95CX LogD: 4.95
Aromatic Rings: 1Heavy Atoms: 30QED Weighted: 0.55Np Likeness Score: -0.06

References

1. Liu Z, Lei Q, Li Y, Xiong L, Song H, Wang Q..  (2011)  Design, synthesis, structure, and acaricidal/insecticidal activity of novel spirocyclic tetronic acid derivatives containing an oxalyl moiety.,  59  (23): [PMID:22044426] [10.1021/jf203722z]

Source