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1,2-bis[3,5-bis(4-Chlorobenzylidene)-4-oxo-piperidin-1-yl]ethane-1,2-dione ID: ALA2391205
PubChem CID: 71699538
Max Phase: Preclinical
Molecular Formula: C40H28Cl4N2O4
Molecular Weight: 742.49
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: O=C1/C(=C/c2ccc(Cl)cc2)CN(C(=O)C(=O)N2C/C(=C\c3ccc(Cl)cc3)C(=O)/C(=C/c3ccc(Cl)cc3)C2)C/C1=C\c1ccc(Cl)cc1
Standard InChI: InChI=1S/C40H28Cl4N2O4/c41-33-9-1-25(2-10-33)17-29-21-45(22-30(37(29)47)18-26-3-11-34(42)12-4-26)39(49)40(50)46-23-31(19-27-5-13-35(43)14-6-27)38(48)32(24-46)20-28-7-15-36(44)16-8-28/h1-20H,21-24H2/b29-17+,30-18+,31-19+,32-20+
Standard InChI Key: JQVFJKDAHJJSPL-BIDHLLRRSA-N
Molfile:
RDKit 2D
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M END 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: 742.49Molecular Weight (Monoisotopic): 740.0803AlogP: 8.76#Rotatable Bonds: 4Polar Surface Area: 74.76Molecular Species: NEUTRALHBA: 4HBD: ┄#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): ┄#RO5 Violations (Lipinski): 2CX Acidic pKa: ┄CX Basic pKa: ┄CX LogP: 9.62CX LogD: 9.62Aromatic Rings: 4Heavy Atoms: 50QED Weighted: 0.15Np Likeness Score: -0.28
References 1. Das S, Das U, Michel D, Gorecki DK, Dimmock JR.. (2013) Novel 3,5-bis(arylidene)-4-piperidone dimers: potent cytotoxins against colon cancer cells., 64 [PMID:23644215 ] [10.1016/j.ejmech.2013.03.055 ] 2. Santiago-Vazquez Y, Das S, Das U, Robles-Escajeda E, Ortega NM, Lema C, Varela-Ramírez A, Aguilera RJ, Balzarini J, De Clercq E, Dimmock SG, Gorecki DK, Dimmock JR.. (2014) Novel 3,5-bis(arylidene)-4-oxo-1-piperidinyl dimers: structure-activity relationships and potent antileukemic and antilymphoma cytotoxicity., 77 [PMID:24657568 ] [10.1016/j.ejmech.2014.03.009 ]