ID: ALA4111342

Max Phase: Preclinical

Molecular Formula: C10H21NO5

Molecular Weight: 235.28

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOCCN1C[C@H](O)[C@@H](O)[C@H](O)[C@H]1CO

Standard InChI:  InChI=1S/C10H21NO5/c1-2-16-4-3-11-5-8(13)10(15)9(14)7(11)6-12/h7-10,12-15H,2-6H2,1H3/t7-,8+,9-,10-/m1/s1

Standard InChI Key:  MNSFMAWUKDBQJX-UTINFBMNSA-N

Associated Targets(non-human)

Lysosomal alpha-glucosidase 58 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: 235.28Molecular Weight (Monoisotopic): 235.1420AlogP: -2.22#Rotatable Bonds: 5
Polar Surface Area: 93.39Molecular Species: NEUTRALHBA: 6HBD: 4
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.90CX Basic pKa: 7.64CX LogP: -2.19CX LogD: -2.63
Aromatic Rings: 0Heavy Atoms: 16QED Weighted: 0.40Np Likeness Score: 0.82

References

1.  (2015)  Method for the treatment of pompe disease using 1-deoxynojirimycin and derivatives, 

Source

Source(1):