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O-(D-glucopyranosylidene)amino-Z-N-2,1,3-Benzothiadiazol-5-ylcarbamate ID: ALA3787212
Chembl Id: CHEMBL3787212
PubChem CID: 127031609
Max Phase: Preclinical
Molecular Formula: C13H15N5O6S
Molecular Weight: 369.36
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C(Nc1ccc2nsnc2c1)O/N=C1\N[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O
Standard InChI: InChI=1S/C13H15N5O6S/c19-4-8-9(20)10(21)11(22)12(15-8)16-24-13(23)14-5-1-2-6-7(3-5)18-25-17-6/h1-3,8-11,19-22H,4H2,(H,14,23)(H,15,16)/t8-,9-,10+,11-/m1/s1
Standard InChI Key: NMAZAEKGKSSISU-CHWFTXMASA-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: 369.36Molecular Weight (Monoisotopic): 369.0743AlogP: -1.40#Rotatable Bonds: 3Polar Surface Area: 169.42Molecular Species: NEUTRALHBA: 10HBD: 6#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 6#RO5 Violations (Lipinski): 2CX Acidic pKa: 11.99CX Basic pKa: 1.78CX LogP: -1.16CX LogD: -1.16Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.28Np Likeness Score: -0.54
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 ]