ID: ALA2288940

Max Phase: Preclinical

Molecular Formula: C35H34O9

Molecular Weight: 598.65

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc2c(cc1OC)[C@H](OC(=O)Cc1cccc3ccccc13)[C@H]1COC(=O)[C@@H]1[C@@H]2c1cc(OC)c(OC)c(OC)c1

Standard InChI:  InChI=1S/C35H34O9/c1-38-26-16-23-24(17-27(26)39-2)33(44-30(36)15-20-11-8-10-19-9-6-7-12-22(19)20)25-18-43-35(37)32(25)31(23)21-13-28(40-3)34(42-5)29(14-21)41-4/h6-14,16-17,25,31-33H,15,18H2,1-5H3/t25-,31+,32-,33-/m0/s1

Standard InChI Key:  MPIDUNOHMLTMQF-NNFCHQEDSA-N

Associated Targets(non-human)

Mythimna separata 3306 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: 598.65Molecular Weight (Monoisotopic): 598.2203AlogP: 5.64#Rotatable Bonds: 9
Polar Surface Area: 98.75Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: CX LogP: 4.95CX LogD: 4.95
Aromatic Rings: 4Heavy Atoms: 44QED Weighted: 0.23Np Likeness Score: 0.86

References

1. He S, Shao Y, Fan L, Che Z, Xu H, Zhi X, Wang J, Yao X, Qu H..  (2013)  Synthesis and quantitative structure-activity relationship (QSAR) study of novel 4-acyloxypodophyllotoxin derivatives modified in the A and C rings as insecticidal agents.,  61  (3): [PMID:23278333] [10.1021/jf305011n]

Source