ID: ALA2228813

Max Phase: Preclinical

Molecular Formula: C29H33NO5

Molecular Weight: 475.59

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCN(C(=O)C(=O)OC1=C(c2c(C)cc(C)cc2C)C(=O)OC12CCCC2)c1ccc(C)cc1C

Standard InChI:  InChI=1S/C29H33NO5/c1-7-30(22-11-10-17(2)14-19(22)4)26(31)28(33)34-25-24(23-20(5)15-18(3)16-21(23)6)27(32)35-29(25)12-8-9-13-29/h10-11,14-16H,7-9,12-13H2,1-6H3

Standard InChI Key:  VEJGPMICBAKBAN-UHFFFAOYSA-N

Associated Targets(non-human)

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

Tetranychus cinnabarinus 1124 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: 475.59Molecular Weight (Monoisotopic): 475.2359AlogP: 5.41#Rotatable Bonds: 4
Polar Surface Area: 72.91Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 7.14CX LogD: 7.14
Aromatic Rings: 2Heavy Atoms: 35QED Weighted: 0.44Np Likeness Score: -0.32

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