ID: ALA5281385

Max Phase: Preclinical

Molecular Formula: C28H22O6

Molecular Weight: 454.48

Associated Items:

Representations

Canonical SMILES:  Oc1ccc(/C=C/c2cc(O)cc3c2C(c2cc(O)cc(O)c2)C(c2ccc(O)cc2)O3)cc1

Standard InChI:  InChI=1S/C28H22O6/c29-20-7-2-16(3-8-20)1-4-18-11-24(33)15-25-26(18)27(19-12-22(31)14-23(32)13-19)28(34-25)17-5-9-21(30)10-6-17/h1-15,27-33H/b4-1+

Standard InChI Key:  FQWLMRXWKZGLFI-DAFODLJHSA-N

Associated Targets(Human)

Huh-7.5 200 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hepatitis C virus 23859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 454.48Molecular Weight (Monoisotopic): 454.1416AlogP: 5.65#Rotatable Bonds: 4
Polar Surface Area: 110.38Molecular Species: NEUTRALHBA: 6HBD: 5
#RO5 Violations: 1HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 1
CX Acidic pKa: 8.51CX Basic pKa: CX LogP: 5.96CX LogD: 5.93
Aromatic Rings: 4Heavy Atoms: 34QED Weighted: 0.25Np Likeness Score: 1.28

References

1. Mattio LM, Catinella G, Pinto A, Dallavalle S..  (2020)  Natural and nature-inspired stilbenoids as antiviral agents.,  202  [PMID:32652408] [10.1016/j.ejmech.2020.112541]

Source