ID: ALA4096943

Max Phase: Preclinical

Molecular Formula: C25H24O3

Molecular Weight: 372.46

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1(C)C=Cc2cc(OCc3ccccc3)c(OCc3ccccc3)cc2O1

Standard InChI:  InChI=1S/C25H24O3/c1-25(2)14-13-21-15-23(26-17-19-9-5-3-6-10-19)24(16-22(21)28-25)27-18-20-11-7-4-8-12-20/h3-16H,17-18H2,1-2H3

Standard InChI Key:  DAEGRMCFFPVKAH-UHFFFAOYSA-N

Associated Targets(Human)

Toll-like receptor 3 331 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: 372.46Molecular Weight (Monoisotopic): 372.1725AlogP: 6.03#Rotatable Bonds: 6
Polar Surface Area: 27.69Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 6.01CX LogD: 6.01
Aromatic Rings: 3Heavy Atoms: 28QED Weighted: 0.53Np Likeness Score: 0.88

References

1. Zhang L, Dewan V, Yin H..  (2017)  Discovery of Small Molecules as Multi-Toll-like Receptor Agonists with Proinflammatory and Anticancer Activities.,  60  (12): [PMID:28537730] [10.1021/acs.jmedchem.7b00419]

Source