ID: ALA162077

Max Phase: Preclinical

Molecular Formula: C6H12O5

Molecular Weight: 164.16

Molecule Type: Small molecule

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C6H12O5/c7-1-4-6(10)5(9)3(8)2-11-4/h3-10H,1-2H2/t3-,4+,5+,6-/m0/s1

Standard InChI Key:  MPCAJMNYNOGXPB-KCDKBNATSA-N

Associated Targets(non-human)

Beta-glucosidase 120 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Beta-galactosidase 1278 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 164.16Molecular Weight (Monoisotopic): 164.0685AlogP: -2.54#Rotatable Bonds: 1
Polar Surface Area: 90.15Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.66CX Basic pKa: CX LogP: -2.57CX LogD: -2.57
Aromatic Rings: 0Heavy Atoms: 11QED Weighted: 0.34Np Likeness Score: 2.49

References

1. Field RA, Haines AH, Chrystal EJ.  (1991)  The Interaction of Anhydroalditols with Sweet-Almond -glucosidase and Escherichia coli -galactosidase: implications for the design of potent glycosidase inhibitors,  (12): [10.1016/S0960-894X(01)81044-1]

Source