ID: ALA5269797

Max Phase: Preclinical

Molecular Formula: C8H14FNO4

Molecular Weight: 207.20

Associated Items:

Representations

Canonical SMILES:  OC[C@@H]1[C@@H](O)[C@H](O)[C@H]2[C@H](O)[C@@H](F)CN21

Standard InChI:  InChI=1S/C8H14FNO4/c9-3-1-10-4(2-11)7(13)8(14)5(10)6(3)12/h3-8,11-14H,1-2H2/t3-,4+,5+,6+,7+,8+/m0/s1

Standard InChI Key:  HVKNJBFAJLQLGG-GUHFPMLUSA-N

Associated Targets(non-human)

Alpha-glucosidase 187 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alpha-mannosidase 234 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alpha-galactosidase 362 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Alpha-L-fucosidase 1 358 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: 207.20Molecular Weight (Monoisotopic): 207.0907AlogP: -2.53#Rotatable Bonds: 1
Polar Surface Area: 84.16Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.88CX Basic pKa: 6.97CX LogP: -2.35CX LogD: -2.49
Aromatic Rings: 0Heavy Atoms: 14QED Weighted: 0.38Np Likeness Score: 1.37

References

1. Li YX, Wang JZ, Shimadate Y, Kise M, Kato A, Jia YM, Fleet GWJ, Yu CY..  (2022)  C-6 fluorinated casuarines as highly potent and selective amyloglucosidase inhibitors: Synthesis and structure-activity relationship study.,  244  [PMID:36332547] [10.1016/j.ejmech.2022.114852]

Source