(E)-5,7,3',4',5'-Pentamethoxyflavan-7-oxy-N'-(3,4-dichlorobenzylidene)acetohydrazide

ID: ALA5196478

Chembl Id: CHEMBL5196478

PubChem CID: 168285507

Max Phase: Preclinical

Molecular Formula: C28H28Cl2N2O7

Molecular Weight: 575.45

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(OCC(=O)N/N=C/c2ccc(Cl)c(Cl)c2)cc2c1CCC(c1cc(OC)c(OC)c(OC)c1)O2

Standard InChI:  InChI=1S/C28H28Cl2N2O7/c1-34-23-12-18(38-15-27(33)32-31-14-16-5-7-20(29)21(30)9-16)13-24-19(23)6-8-22(39-24)17-10-25(35-2)28(37-4)26(11-17)36-3/h5,7,9-14,22H,6,8,15H2,1-4H3,(H,32,33)/b31-14+

Standard InChI Key:  ISNPRBWPTTTXOE-XAZZYMPDSA-N

Alternative Forms

  1. Parent:

    ALA5196478

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Associated Targets(Human)

Huh7.5.1 (171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hepatovirus A (249 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

Calculated Properties

Molecular Weight: 575.45Molecular Weight (Monoisotopic): 574.1274AlogP: 5.62#Rotatable Bonds: 10
Polar Surface Area: 96.84Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 2HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 11.57CX Basic pKa: 0.70CX LogP: 5.31CX LogD: 5.31
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.25Np Likeness Score: -0.34

References

1. Shi S, Zheng X, Suzuki R, Li Z, Shiota T, Wang J, Hirai-Yuki A, Liu Q, Muramatsu M, Song SJ..  (2022)  Novel flavonoid hybrids as potent antiviral agents against hepatitis A: Design, synthesis and biological evaluation.,  238  [PMID:35597006] [10.1016/j.ejmech.2022.114452]

Source