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Methyl 2-O-(2-nitrobenzoyl)-3-O-(4-methylbenzoyl)-beta-D-talopyranoside ID: ALA5175908
Chembl Id: CHEMBL5175908
PubChem CID: 164513431
Max Phase: Preclinical
Molecular Formula: C22H23NO10
Molecular Weight: 461.42
Associated Items:
Names and Identifiers Canonical SMILES: CO[C@@H]1O[C@H](CO)[C@H](O)[C@H](OC(=O)c2ccc(C)cc2)[C@@H]1OC(=O)c1ccccc1[N+](=O)[O-]
Standard InChI: InChI=1S/C22H23NO10/c1-12-7-9-13(10-8-12)20(26)32-18-17(25)16(11-24)31-22(30-2)19(18)33-21(27)14-5-3-4-6-15(14)23(28)29/h3-10,16-19,22,24-25H,11H2,1-2H3/t16-,17+,18+,19+,22-/m1/s1
Standard InChI Key: CFXAQLIZQHBOAM-NOYKIMNZSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 461.42Molecular Weight (Monoisotopic): 461.1322AlogP: 1.38#Rotatable Bonds: 7Polar Surface Area: 154.66Molecular Species: NEUTRALHBA: 10HBD: 2#RO5 Violations: ┄HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 1CX Acidic pKa: 13.01CX Basic pKa: ┄CX LogP: 3.15CX LogD: 3.15Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.35Np Likeness Score: 0.55
References 1. Bum-Erdene K, Collins PM, Hugo MW, Tarighat SS, Fei F, Kishor C, Leffler H, Nilsson UJ, Groffen J, Grice ID, Heisterkamp N, Blanchard H.. (2022) Novel Selective Galectin-3 Antagonists Are Cytotoxic to Acute Lymphoblastic Leukemia., 65 (8.0): [PMID:35427125 ] [10.1021/acs.jmedchem.1c01296 ]