ID: ALA3344205

Max Phase: Preclinical

Molecular Formula: C15H31NO4

Molecular Weight: 289.42

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCCCCCCCN1C[C@@H](O)C(O)(CCO)[C@@H](O)C1

Standard InChI:  InChI=1S/C15H31NO4/c1-2-3-4-5-6-7-9-16-11-13(18)15(20,8-10-17)14(19)12-16/h13-14,17-20H,2-12H2,1H3/t13-,14+,15?

Standard InChI Key:  KHTADPXNKIPBPW-YIONKMFJSA-N

Associated Targets(Human)

Lysosomal alpha-mannosidase 172 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

PBMC 10003 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

B cell 126 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Jurkat 10389 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: 289.42Molecular Weight (Monoisotopic): 289.2253AlogP: 0.50#Rotatable Bonds: 9
Polar Surface Area: 84.16Molecular Species: NEUTRALHBA: 5HBD: 4
#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 4#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.65CX Basic pKa: 8.49CX LogP: 0.52CX LogD: -0.60
Aromatic Rings: 0Heavy Atoms: 20QED Weighted: 0.46Np Likeness Score: 0.72

References

1. Markad PR, Sonawane DP, Ghosh S, Chopade BA, Kumbhar N, Louat T, Herman J, Waer M, Herdewijn P, Dhavale DD..  (2014)  γ-Hydroxyethyl piperidine iminosugar and N-alkylated derivatives: a study of their activity as glycosidase inhibitors and as immunosuppressive agents.,  22  (21): [PMID:25305010] [10.1016/j.bmc.2014.09.034]

Source