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O-(D-glucopyranosylidene)amino-Z-N-2-Chloro-6-(trifluoromethyl)phenylcarbamate ID: ALA3786410
Chembl Id: CHEMBL3786410
PubChem CID: 127031894
Max Phase: Preclinical
Molecular Formula: C14H15ClF3N3O6
Molecular Weight: 413.74
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C(Nc1c(Cl)cccc1C(F)(F)F)O/N=C1\N[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Standard InChI: InChI=1S/C14H15ClF3N3O6/c15-6-3-1-2-5(14(16,17)18)8(6)20-13(26)27-21-12-11(25)10(24)9(23)7(4-22)19-12/h1-3,7,9-11,22-25H,4H2,(H,19,21)(H,20,26)/t7-,9-,10+,11-/m1/s1
Standard InChI Key: DDYYAIXYMMMODK-CZULRBLNSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 413.74Molecular Weight (Monoisotopic): 413.0601AlogP: 0.27#Rotatable Bonds: 3Polar Surface Area: 143.64Molecular Species: NEUTRALHBA: 7HBD: 6#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 6#RO5 Violations (Lipinski): 1CX Acidic pKa: 11.38CX Basic pKa: 1.78CX LogP: 0.18CX LogD: 0.18Aromatic Rings: 1Heavy Atoms: 27QED Weighted: 0.31Np Likeness Score: -0.35
References 1. Wang J, Wang X, Zhao Y, Ma X, Wan Y, Chen Z, Chen H, Gan H, Li J, Li L, Wang PG, Zhao W. (2016) Synthesis and biological evaluation ofd-gluconhydroximo-1,5-lactam and its oxime-substituted derivatives as pharmacological chaperones for the treatment of Gaucher disease, 7 (2): [10.1039/C5MD00501A ]