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alpha-D-Ribopiranose Tetrakis(2,3,4-trihydroxybenzoate) ID: ALA4555734
Chembl Id: CHEMBL4555734
PubChem CID: 155557002
Max Phase: Preclinical
Molecular Formula: C33H26O21
Molecular Weight: 758.55
Molecule Type: Unknown
Associated Items:
Names and Identifiers Canonical SMILES: O=C(O[C@H]1OC[C@@H](OC(=O)c2ccc(O)c(O)c2O)[C@@H](OC(=O)c2ccc(O)c(O)c2O)[C@H]1OC(=O)c1ccc(O)c(O)c1O)c1ccc(O)c(O)c1O
Standard InChI: InChI=1S/C33H26O21/c34-14-5-1-10(19(38)23(14)42)29(46)51-18-9-50-33(54-32(49)13-4-8-17(37)26(45)22(13)41)28(53-31(48)12-3-7-16(36)25(44)21(12)40)27(18)52-30(47)11-2-6-15(35)24(43)20(11)39/h1-8,18,27-28,33-45H,9H2/t18-,27-,28-,33-/m1/s1
Standard InChI Key: GTMXROBUKMAWHP-NYECIAITSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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: 758.55Molecular Weight (Monoisotopic): 758.0967AlogP: 1.34#Rotatable Bonds: 8Polar Surface Area: 357.19Molecular Species: NEUTRALHBA: 21HBD: 12#RO5 Violations: 3HBA (Lipinski): 21HBD (Lipinski): 12#RO5 Violations (Lipinski): 3CX Acidic pKa: 7.93CX Basic pKa: ┄CX LogP: 6.64CX LogD: 6.57Aromatic Rings: 4Heavy Atoms: 54QED Weighted: 0.07Np Likeness Score: 0.63
References 1. G-Doyagüez E, Carrero P, Madrona A, Rodriguez-Salamanca P, Martínez-Gualda B, Camarasa MJ, Jimeno ML, Bennallack PR, Finnell JG, Tsang TM, Christensen KA, San-Félix A, Rogers MS.. (2019) Galloyl Carbohydrates with Antiangiogenic Activity Mediated by Capillary Morphogenesis Gene 2 (CMG2) Protein Binding., 62 (8): [PMID:30964669 ] [10.1021/acs.jmedchem.8b01988 ]