ID: ALA4091275

Max Phase: Preclinical

Molecular Formula: C21H22O5

Molecular Weight: 354.40

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C/C=C/c1cc(OC)c2c(c1)[C@H](C)[C@@H](c1cc(OC)c3c(c1)OCO3)O2

Standard InChI:  InChI=1S/C21H22O5/c1-5-6-13-7-15-12(2)19(26-20(15)16(8-13)22-3)14-9-17(23-4)21-18(10-14)24-11-25-21/h5-10,12,19H,11H2,1-4H3/b6-5+/t12-,19-/m0/s1

Standard InChI Key:  UIWUAELYQAENKN-FNINDUDTSA-N

Associated Targets(non-human)

Sialidase A 49 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: 354.40Molecular Weight (Monoisotopic): 354.1467AlogP: 4.70#Rotatable Bonds: 4
Polar Surface Area: 46.15Molecular Species: NEUTRALHBA: 5HBD: 0
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.44CX LogD: 4.44
Aromatic Rings: 2Heavy Atoms: 26QED Weighted: 0.80Np Likeness Score: 1.60

References

1. Park JY, Hwan Lim S, Ram Kim B, Jae Jeong H, Kwon HJ, Song GY, Bae Ryu Y, Song Lee W..  (2017)  Sialidase inhibitory activity of diarylnonanoid and neolignan compounds extracted from the seeds of Myristica fragrans.,  27  (14): [PMID:28551100] [10.1016/j.bmcl.2017.05.055]

Source