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Viridissimaol B ID: ALA4473882
Chembl Id: CHEMBL4473882
PubChem CID: 155536596
Max Phase: Preclinical
Molecular Formula: C41H44O12
Molecular Weight: 728.79
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: COc1cc(C[C@H]2C(=O)OC[C@@H]2Cc2cc(OC)c(O)c(-c3cc(C[C@H]4C(=O)OC[C@@H]4Cc4ccc(OC)c(OC)c4)cc(OC)c3O)c2)ccc1O
Standard InChI: InChI=1S/C41H44O12/c1-47-33-9-7-22(17-35(33)49-3)10-26-20-52-41(46)29(26)13-25-15-31(39(44)37(19-25)51-5)30-14-24(18-36(50-4)38(30)43)11-27-21-53-40(45)28(27)12-23-6-8-32(42)34(16-23)48-2/h6-9,14-19,26-29,42-44H,10-13,20-21H2,1-5H3/t26-,27-,28+,29+/m0/s1
Standard InChI Key: GWOWIVFDQIIGNT-QUAHOIDUSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 728.79Molecular Weight (Monoisotopic): 728.2833AlogP: 5.66#Rotatable Bonds: 14Polar Surface Area: 159.44Molecular Species: NEUTRALHBA: 12HBD: 3#RO5 Violations: 3HBA (Lipinski): 12HBD (Lipinski): 3#RO5 Violations (Lipinski): 3CX Acidic pKa: 9.10CX Basic pKa: ┄CX LogP: 6.40CX LogD: 6.39Aromatic Rings: 4Heavy Atoms: 53QED Weighted: 0.14Np Likeness Score: 0.86
References 1. Huh J, Song JH, Kim SR, Cho HM, Ko HJ, Yang H, Sung SH.. (2019) Lignan Dimers from Forsythia viridissima Roots and Their Antiviral Effects., 82 (2): [PMID:30676026 ] [10.1021/acs.jnatprod.8b00590 ]