ID: ALA2414741

Max Phase: Preclinical

Molecular Formula: C16H23NO5

Molecular Weight: 309.36

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  OC[C@H]1O[C@@H](CNC/C=C/c2ccccc2)[C@H](O)[C@@H](O)[C@@H]1O

Standard InChI:  InChI=1S/C16H23NO5/c18-10-13-15(20)16(21)14(19)12(22-13)9-17-8-4-7-11-5-2-1-3-6-11/h1-7,12-21H,8-10H2/b7-4+/t12-,13+,14-,15+,16+/m0/s1

Standard InChI Key:  LHEKRJPKKLZBDY-SKWGZQBISA-N

Associated Targets(non-human)

Sucrase-isomaltase 908 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Acidic alpha-glucosidase 551 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Oligo-1,6-glucosidase 218 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: 309.36Molecular Weight (Monoisotopic): 309.1576AlogP: -0.87#Rotatable Bonds: 6
Polar Surface Area: 102.18Molecular Species: NEUTRALHBA: 6HBD: 5
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 5#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.60CX Basic pKa: 8.18CX LogP: -0.54CX LogD: -1.39
Aromatic Rings: 1Heavy Atoms: 22QED Weighted: 0.44Np Likeness Score: 0.99

References

1. Bian X, Fan X, Ke C, Luan Y, Zhao G, Zeng A..  (2013)  Synthesis and α-glucosidase inhibitory activity evaluation of N-substituted aminomethyl-β-d-glucopyranosides.,  21  (17): [PMID:23810673] [10.1016/j.bmc.2013.06.002]

Source