egonol 3''-methyl ether

ID: ALA3361248

Chembl Id: CHEMBL3361248

PubChem CID: 118724835

Max Phase: Preclinical

Molecular Formula: C20H20O5

Molecular Weight: 340.38

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  COCCCc1cc(OC)c2oc(-c3ccc4c(c3)OCO4)cc2c1

Standard InChI:  InChI=1S/C20H20O5/c1-21-7-3-4-13-8-15-11-17(25-20(15)19(9-13)22-2)14-5-6-16-18(10-14)24-12-23-16/h5-6,8-11H,3-4,7,12H2,1-2H3

Standard InChI Key:  BNNSZVXJKPLGHT-UHFFFAOYSA-N

Alternative Forms

  1. Parent:

    ALA3361248

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Associated Targets(Human)

A2058 (690 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

Calculated Properties

Molecular Weight: 340.38Molecular Weight (Monoisotopic): 340.1311AlogP: 4.42#Rotatable Bonds: 6
Polar Surface Area: 50.06Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.77CX LogD: 3.77
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.62Np Likeness Score: 0.37

References

1. Hajdu Z, Haskó J, Krizbai IA, Wilhelm I, Jedlinszki N, Fazakas C, Molnár J, Forgo P, Hohmann J, Csupor D..  (2014)  Evaluation of lignans from Heliopsis helianthoides var. scabra for their potential antimetastatic effects in the brain.,  77  (12): [PMID:25479041] [10.1021/np500508y]

Source