BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

672 related articles for article (PubMed ID: 17266307)

  • 1. Modeling the 2-His-1-carboxylate facial triad: iron-catecholato complexes as structural and functional models of the extradiol cleaving dioxygenases.
    Bruijnincx PC; Lutz M; Spek AL; Hagen WR; Weckhuysen BM; van Koten G; Gebbink RJ
    J Am Chem Soc; 2007 Feb; 129(8):2275-86. PubMed ID: 17266307
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Iron(III) complexes of tripodal monophenolate ligands as models for non-heme catechol dioxygenase enzymes: correlation of dioxygenase activity with ligand stereoelectronic properties.
    Mayilmurugan R; Visvaganesan K; Suresh E; Palaniandavar M
    Inorg Chem; 2009 Sep; 48(18):8771-83. PubMed ID: 19694480
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Iron(III) complexes of tridentate 3N ligands as functional models for catechol dioxygenases: the role of ligand N-alkyl substitution and solvent on reaction rate and product selectivity.
    Visvaganesan K; Mayilmurugan R; Suresh E; Palaniandavar M
    Inorg Chem; 2007 Nov; 46(24):10294-306. PubMed ID: 17958355
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel iron(III) complexes of sterically hindered 4N ligands: regioselectivity in biomimetic extradiol cleavage of catechols.
    Mayilmurugan R; Stoeckli-Evans H; Palaniandavar M
    Inorg Chem; 2008 Aug; 47(15):6645-58. PubMed ID: 18597419
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A functional model of extradiol-cleaving catechol dioxygenases: mimicking the 2-his-1-carboxylate facial triad.
    Paria S; Halder P; Paine TK
    Inorg Chem; 2010 May; 49(10):4518-23. PubMed ID: 20392074
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis, structure, spectra and reactivity of iron(III) complexes of facially coordinating and sterically hindering 3N ligands as models for catechol dioxygenases.
    Sundaravel K; Dhanalakshmi T; Suresh E; Palaniandavar M
    Dalton Trans; 2008 Dec; (48):7012-25. PubMed ID: 19050788
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Iron(III)-catecholato complexes as structural and functional models of the intradiol-cleaving catechol dioxygenases.
    Bruijnincx PC; Lutz M; Spek AL; Hagen WR; van Koten G; Gebbink RJ
    Inorg Chem; 2007 Oct; 46(20):8391-402. PubMed ID: 17722878
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional models for catechol dioxygenases: iron(III) complexes of cis-facially coordinating linear 3N ligands.
    Velusamy M; Mayilmurugan R; Palaniandavar M
    J Inorg Biochem; 2005 May; 99(5):1032-42. PubMed ID: 15833326
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Iron(III) complexes of sterically hindered tetradentate monophenolate ligands as functional models for catechol 1,2-dioxygenases: the role of ligand stereoelectronic properties.
    Velusamy M; Mayilmurugan R; Palaniandavar M
    Inorg Chem; 2004 Oct; 43(20):6284-93. PubMed ID: 15446874
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synthesis, structure, spectra and reactivity of iron(III) complexes of imidazole and pyrazole containing ligands as functional models for catechol dioxygenases.
    Dhanalakshmi T; Suresh E; Palaniandavar M
    Dalton Trans; 2009 Oct; (39):8317-28. PubMed ID: 19789784
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel iron(III) complexes of tripodal and linear tetradentate bis(phenolate) ligands: close relevance to intradiol-cleaving catechol dioxygenases.
    Velusamy M; Palaniandavar M; Gopalan RS; Kulkarni GU
    Inorg Chem; 2003 Dec; 42(25):8283-93. PubMed ID: 14658880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Iron(III) complexes of N2O and N3O donor ligands as functional models for catechol dioxygenase enzymes: ether oxygen coordination tunes the regioselectivity and reactivity.
    Sundaravel K; Suresh E; Saminathan K; Palaniandavar M
    Dalton Trans; 2011 Aug; 40(32):8092-107. PubMed ID: 21766098
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel square pyramidal iron(III) complexes of linear tetradentate bis(phenolate) ligands as structural and reactive models for intradiol-cleaving 3,4-PCD enzymes: Quinone formation vs. intradiol cleavage.
    Mayilmurugan R; Sankaralingam M; Suresh E; Palaniandavar M
    Dalton Trans; 2010 Oct; 39(40):9611-25. PubMed ID: 20835480
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Iron(III) complexes of certain meridionally coordinating tridentate ligands as models for non-heme iron enzymes: the role of carboxylate coordination.
    Dhanalakshmi T; Bhuvaneshwari M; Palaniandavar M
    J Inorg Biochem; 2006 Sep; 100(9):1527-34. PubMed ID: 16814389
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 4-nitrocatechol as a probe of a Mn(II)-dependent extradiol-cleaving catechol dioxygenase (MndD): comparison with relevant Fe(II) and Mn(II) model complexes.
    Reynolds MF; Costas M; Ito M; Jo DH; Tipton AA; Whiting AK; Que L
    J Biol Inorg Chem; 2003 Feb; 8(3):263-72. PubMed ID: 12589562
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Quantum chemical studies of dioxygen activation by mononuclear non-heme iron enzymes with the 2-His-1-carboxylate facial triad.
    Bassan A; Borowski T; Siegbahn PE
    Dalton Trans; 2004 Oct; (20):3153-62. PubMed ID: 15483690
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Studies of iron(II) and iron(III) complexes with fac-N2O, cis-N2O2 and N2O3 donor ligands: models for the 2-His 1-carboxylate motif of non-heme iron monooxygenases.
    Cappillino PJ; Miecznikowski JR; Tyler LA; Tarves PC; McNally JS; Lo W; Kasibhatla BS; Krzyaniak MD; McCracken J; Wang F; Armstrong WH; Caradonna JP
    Dalton Trans; 2012 May; 41(18):5662-77. PubMed ID: 22434362
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tetranuclear iron(III) complexes of an octadentate pyridine-carboxylate ligand and their catalytic activity in alkane oxidation by hydrogen peroxide.
    Gutkina EA; Trukhan VM; Pierpont CG; Mkoyan S; Strelets VV; Nordlander E; Shteinman AA
    Dalton Trans; 2006 Jan; (3):492-501. PubMed ID: 16395449
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A phenolate-induced trans influence: crystallographic evidence for unusual asymmetric coordination of an alpha-diimine in ternary complexes of iron(III) possessing biologically relevant hetero-donor N-centered tripodal ligands.
    Shongwe MS; Kaschula CH; Adsetts MS; Ainscough EW; Brodie AM; Morris MJ
    Inorg Chem; 2005 May; 44(9):3070-9. PubMed ID: 15847411
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oxygen activation by nonheme iron(II) complexes: alpha-keto carboxylate versus carboxylate.
    Mehn MP; Fujisawa K; Hegg EL; Que L
    J Am Chem Soc; 2003 Jul; 125(26):7828-42. PubMed ID: 12823001
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.