Pucci et al., 2013 - Google Patents
Improving the bioactivity of Zn (II)-curcumin based complexesPucci et al., 2013
View PDF- Document ID
- 14390508169318476947
- Author
- Pucci D
- Crispini A
- Mendiguchía B
- Pirillo S
- Ghedini M
- Morelli S
- De Bartolo L
- Publication year
- Publication venue
- Dalton Transactions
External Links
Snippet
New Zn (II)-curcumin based heteroleptic complexes (1–5) have been synthesized and fully characterized, with the aim to improve the bioactivity of the precursor derivative [(bpy-9) Zn (curc) Cl](A), a potentially intercalating antitumor agent recently reported. Some structural …
- 239000004148 curcumin 0 title abstract description 20
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P-C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Pucci et al. | Improving the bioactivity of Zn (II)-curcumin based complexes | |
Subarkhan et al. | Synthesis and molecular structure of arene ruthenium (II) benzhydrazone complexes: impact of substitution at the chelating ligand and arene moiety on antiproliferative activity | |
Colina-Vegas et al. | Half sandwich Ru (II)-acylthiourea complexes: DNA/HSA-binding, anti-migration and cell death in a human breast tumor cell line | |
Subarkhan et al. | Ruthenium (II) arene complexes containing benzhydrazone ligands: synthesis, structure and antiproliferative activity | |
Arcau et al. | Luminescent alkynyl-gold (I) coumarin derivatives and their biological activity | |
Čanović et al. | Impact of aromaticity on anticancer activity of polypyridyl ruthenium (II) complexes: synthesis, structure, DNA/protein binding, lipophilicity and anticancer activity | |
Pierroz et al. | Molecular and cellular characterization of the biological effects of ruthenium (II) complexes incorporating 2-pyridyl-2-pyrimidine-4-carboxylic acid | |
Chen et al. | Lysosome-targeted iridium (III) compounds with pyridine-triphenylamine Schiff base ligands: syntheses, antitumor applications and mechanisms | |
Lo et al. | Iridium (III) complexes as therapeutic and bioimaging reagents for cellular applications | |
Gimeno et al. | Conjugates of ferrocene with biological compounds. Coordination to gold complexes and antitumoral properties | |
Yu et al. | Supramolecular enhancement of aggregation-induced emission and its application in cancer cell imaging | |
Cafeo et al. | Drug delivery with a calixpyrrole–trans-Pt (II) complex | |
Galassi et al. | Synthesis and characterization of azolate gold (I) phosphane complexes as thioredoxin reductase inhibiting antitumor agents | |
Mendiguchia et al. | Zn (II) and Cu (II) complexes containing bioactive O, O-chelated ligands: homoleptic and heteroleptic metal-based biomolecules | |
Gavara et al. | Study of the effect of the chromophore and nuclearity on the aggregation and potential biological activity of gold (I) alkynyl complexes | |
Joksović et al. | Synthesis, characterization and antitumor activity of novel N-substituted α-amino acids containing ferrocenyl pyrazole-moiety | |
Yilmaz et al. | Synthesis, structures and biomolecular interactions of new silver (I) 5, 5-diethylbarbiturate complexes of monophosphines targeting Gram-positive bacteria and breast cancer cells | |
Czerwińska et al. | Cytotoxic gold (III) complexes incorporating a 2, 2′: 6′, 2′′-terpyridine ligand framework–the impact of the substituent in the 4′-position of a terpy ring | |
Sarkar et al. | Remarkable visible light-triggered cytotoxicity of mitochondria targeting mixed-ligand cobalt (III) complexes of curcumin and phenanthroline bases binding to human serum albumin | |
Gupta et al. | Anticancer activity of large metalla-assemblies built from half-sandwich complexes | |
Zahirović et al. | Type of complex–BSA binding forces affected by different coordination modes of alliin in novel water-soluble ruthenium complexes | |
Kozieł et al. | Anticancer potency of novel organometallic Ir (III) complexes with phosphine derivatives of fluoroquinolones encapsulated in polymeric micelles | |
Mondal et al. | Hypoxia efficient and glutathione-resistant cytoselective ruthenium (II)-p-cymene-arylimidazophenanthroline complexes: biomolecular interaction and live cell imaging | |
Icsel et al. | Structures and anticancer activity of chlorido platinum (II) saccharinate complexes with mono-and dialkylphenylphosphines | |
Subran et al. | Amberlite IR-120 (H)-mediated “on water” synthesis of novel anticancer ruthenium (II)–p-cymene 2-pyridinylbenzothiazole (BTZ), 2-pyridinylbenzoxazole (BOZ) & 2-pyridinylbenzimidazole (BIZ) scaffolds |