ID: ALA3361249

Max Phase: Preclinical

Molecular Formula: C22H20O8

Molecular Weight: 412.39

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COC(=O)/C(=C/c1ccc2c(c1)OCO2)C(Cc1ccc2c(c1)OCO2)C(=O)OC

Standard InChI:  InChI=1S/C22H20O8/c1-25-21(23)15(7-13-3-5-17-19(9-13)29-11-27-17)16(22(24)26-2)8-14-4-6-18-20(10-14)30-12-28-18/h3-7,9-10,16H,8,11-12H2,1-2H3/b15-7+

Standard InChI Key:  MHPJAZYITXHVOI-VIZOYTHASA-N

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

Properties

Molecular Weight: 412.39Molecular Weight (Monoisotopic): 412.1158AlogP: 2.73#Rotatable Bonds: 6
Polar Surface Area: 89.52Molecular Species: NEUTRALHBA: 8HBD: 0
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.55CX LogD: 3.55
Aromatic Rings: 2Heavy Atoms: 30QED Weighted: 0.53Np Likeness Score: 0.60

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