ID: ALA146193

Max Phase: Preclinical

Molecular Formula: C20H18O5

Molecular Weight: 338.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=CCOc1ccc2c(=O)c3cccc(CC(=O)OC)c3oc2c1C

Standard InChI:  InChI=1S/C20H18O5/c1-4-10-24-16-9-8-15-18(22)14-7-5-6-13(11-17(21)23-3)20(14)25-19(15)12(16)2/h4-9H,1,10-11H2,2-3H3

Standard InChI Key:  MSBLZYRXYVXYQM-UHFFFAOYSA-N

Associated Targets(Human)

Homo sapiens 32628 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus 284745 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: 338.36Molecular Weight (Monoisotopic): 338.1154AlogP: 3.53#Rotatable Bonds: 5
Polar Surface Area: 65.74Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 3.83CX LogD: 3.83
Aromatic Rings: 3Heavy Atoms: 25QED Weighted: 0.40Np Likeness Score: 0.11

References

1. Gobbi S, Rampa A, Bisi A, Belluti F, Valenti P, Caputo A, Zampiron A, Carrara M..  (2002)  Synthesis and antitumor activity of new derivatives of xanthen-9-one-4-acetic acid.,  45  (22): [PMID:12383019] [10.1021/jm020929p]

Source