ID: ALA5268948

Max Phase: Preclinical

Molecular Formula: C35H32O8

Molecular Weight: 580.63

Associated Items:

Representations

Canonical SMILES:  COc1cc(O)c([C@H](/C=C/C[C@@H](O)CCc2ccc(O)cc2)c2ccc(O)cc2)c2oc(-c3ccc(O)cc3)cc(=O)c12

Standard InChI:  InChI=1S/C35H32O8/c1-42-32-20-29(40)33(35-34(32)30(41)19-31(43-35)23-10-17-27(39)18-11-23)28(22-8-15-26(38)16-9-22)4-2-3-24(36)12-5-21-6-13-25(37)14-7-21/h2,4,6-11,13-20,24,28,36-40H,3,5,12H2,1H3/b4-2+/t24-,28-/m1/s1

Standard InChI Key:  FLIIBLJEEJQQBU-MTKGSJEHSA-N

Associated Targets(non-human)

J774.1 238 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: 580.63Molecular Weight (Monoisotopic): 580.2097AlogP: 6.36#Rotatable Bonds: 10
Polar Surface Area: 140.59Molecular Species: ACIDHBA: 8HBD: 5
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): 2
CX Acidic pKa: 6.32CX Basic pKa: CX LogP: 6.03CX LogD: 4.92
Aromatic Rings: 5Heavy Atoms: 43QED Weighted: 0.12Np Likeness Score: 1.37

References

1. Vanucci-Bacqué C, Bedos-Belval F..  (2021)  Anti-inflammatory activity of naturally occuring diarylheptanoids - A review.,  31  [PMID:33422907] [10.1016/j.bmc.2020.115971]
2. Vanucci-Bacqué C, Bedos-Belval F..  (2021)  Anti-inflammatory activity of naturally occuring diarylheptanoids - A review.,  31  [PMID:33422907] [10.1016/j.bmc.2020.115971]

Source