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ID: ALA3628132
Max Phase: Preclinical
Molecular Formula: C25H24O6
Molecular Weight: 420.46
Molecule Type: Small molecule
Associated Items:
Representations Canonical SMILES: O=C(/C=C/c1ccc(O)c(O)c1)OCCc1cccc(OCCc2cccc(O)c2)c1
Standard InChI: InChI=1S/C25H24O6/c26-21-5-1-3-18(15-21)11-13-30-22-6-2-4-19(16-22)12-14-31-25(29)10-8-20-7-9-23(27)24(28)17-20/h1-10,15-17,26-28H,11-14H2/b10-8+
Standard InChI Key: NIXPUWCVVMXORF-CSKARUKUSA-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
Properties Molecular Weight: 420.46Molecular Weight (Monoisotopic): 420.1573AlogP: 4.22#Rotatable Bonds: 9Polar Surface Area: 96.22Molecular Species: NEUTRALHBA: 6HBD: 3#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0CX Acidic pKa: 9.15CX Basic pKa: CX LogP: 5.47CX LogD: 5.47Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.27Np Likeness Score: 0.41
References 1. Maresca A, Akyuz G, Osman SM, AlOthman Z, Supuran CT.. (2015) Inhibition of mammalian carbonic anhydrase isoforms I-XIV with a series of phenolic acid esters., 23 (22): [PMID:26498394 ] [10.1016/j.bmc.2015.10.014 ]