ID: ALA2409323

Max Phase: Preclinical

Molecular Formula: C28H48N4O5

Molecular Weight: 520.72

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)CN1CCCCCCCCn1cc(COCC23CC4CC(CC(C4)C2)C3)nn1

Standard InChI:  InChI=1S/C28H48N4O5/c33-17-24-26(35)27(36)25(34)16-31(24)7-5-3-1-2-4-6-8-32-15-23(29-30-32)18-37-19-28-12-20-9-21(13-28)11-22(10-20)14-28/h15,20-22,24-27,33-36H,1-14,16-19H2/t20?,21?,22?,24-,25+,26-,27-,28?/m1/s1

Standard InChI Key:  OGAHBWBWPUWLKS-NLTICPCISA-N

Associated Targets(non-human)

Bovine viral diarrhea virus 1 1277 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: 520.72Molecular Weight (Monoisotopic): 520.3625AlogP: 2.11#Rotatable Bonds: 14
Polar Surface Area: 124.10Molecular Species: NEUTRALHBA: 9HBD: 4
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 4#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.90CX Basic pKa: 8.37CX LogP: 2.08CX LogD: 1.08
Aromatic Rings: 1Heavy Atoms: 37QED Weighted: 0.28Np Likeness Score: -0.05

References

1. Howe JD, Smith N, Lee MJ, Ardes-Guisot N, Vauzeilles B, Désiré J, Baron A, Blériot Y, Sollogoub M, Alonzi DS, Butters TD..  (2013)  Novel imino sugar α-glucosidase inhibitors as antiviral compounds.,  21  (16): [PMID:23582447] [10.1016/j.bmc.2013.03.014]

Source