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1

Choy, Tak-Kee, Chih-Yang Wang, Nam Nhut Phan, Hoang Dang Khoa Ta, Gangga Anuraga, Yen-Hsi Liu, Yung-Fu Wu, Kuen-Haur Lee, Jian-Ying Chuang, and Tzu-Jen Kao. "Identification of Dipeptidyl Peptidase (DPP) Family Genes in Clinical Breast Cancer Patients via an Integrated Bioinformatics Approach." Diagnostics 11, no. 7 (July 2, 2021): 1204. http://dx.doi.org/10.3390/diagnostics11071204.

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Breast cancer is a heterogeneous disease involving complex interactions of biological processes; thus, it is important to develop therapeutic biomarkers for treatment. Members of the dipeptidyl peptidase (DPP) family are metalloproteases that specifically cleave dipeptides. This family comprises seven members, including DPP3, DPP4, DPP6, DPP7, DPP8, DPP9, and DPP10; however, information on the involvement of DPPs in breast cancer is lacking in the literature. As such, we aimed to study their roles in this cancerous disease using publicly available databases such as cBioportal, Oncomine, and Ka
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Funston, Alison M., Carleen Cullinane, Kenneth P. Ghiggino, W. David McFadyen, Stanley S. Stylli, and Peter A. Tregloan. "Dipyridophenazine Complexes of Cobalt(III): DNA Photocleavage and Photobiology." Australian Journal of Chemistry 58, no. 3 (2005): 206. http://dx.doi.org/10.1071/ch04206.

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The UV-visible spectroscopy and photochemistry of [Co(en)2(DPPZ)](ClO4)3 (DPPZ = dipyrido[3,2-a:2´,3´-c]-phenazine) in the presence of plasmid DNA and the nucleoside 2´-deoxygaunosine have been investigated. Evidence for the intercalation of the complex with DNA and photoinduced DNA strand breakage is found. The structurally related complexes [Co(en)2(DPPN)]Cl3 and [Co(en)2(DPPA)]Cl2, where DPPN = benzo[i]dipyrido[3,2-a:2´,3´-c]phenazine and DPPA = dipyrido[3,2-a:2´,3´-c] phenazine-11-carboxylic acid, have also been synthesized and characterized. In vitro cytotoxicity studies and photocytotoxi
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QI, Shu Y., Pierre J. RIVIERE, Jerzy TROJNAR, Jean-Louis JUNIEN, and Karen O. AKINSANYA. "Cloning and characterization of dipeptidyl peptidase 10, a new member of an emerging subgroup of serine proteases." Biochemical Journal 373, no. 1 (July 1, 2003): 179–89. http://dx.doi.org/10.1042/bj20021914.

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Two dipeptidyl peptidase IV (DPPIV, DPP4)-related proteins, DPP8 and DPP9, have been identified recently [Abbott, Yu, Woollatt, Sutherland, McCaughan, and Gorrell (2000) Eur. J. Biochem. 267, 6140–6150; Olsen and Wagtmann (2002) Gene 299, 185–193; Qi, Akinsanya, Riviere, and Junien (2002) Patent application WO0231134]. In the present study, we describe the cloning of DPP10, a novel 796-amino-acid protein, with significant sequence identity to DPP4 (32%) and DPP6 (51%) respectively. We propose that DPP10 is a new member of the S9B serine proteases subfamily. The DPP10 gene is located on the lon
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4

Al-Samrai, Osama'a A. Y., Ahmed S. M. Al-Janabi2, and Eman A. Othman1. "Mixed Ligand Complexes of Hg-tetrazole-thiolate with phosphine, Synthesis and spectroscopic studies." Tikrit Journal of Pure Science 24, no. 5 (September 13, 2019): 10. http://dx.doi.org/10.25130/j.v24i5.860.

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Seven new complexes [Hg(k1-ptt)2](1), [Hg(k1-ptt)2(dppm)](2), [Hg(k1-ptt)2(dppe)](3), [Hg(k1-ptt)2(dppp)](4), [Hg(k1-ptt)2(dppb)](5), [Hg(k1-ptt)2(dppf)] (6), and [Hg(k1-ptt)2(PPh3)2] (7) have been synthesized and characterized. The reaction of two moles equivalent of 1-Phenyl-1H-tetrazole-5-thiol (Hptt) with one mole equivalent of Hg(oAc)2.xH2O in ethanol solution afford [Hg(k1-ptt)2] (1). Treatment of (1) with one mole equivalent of diphos (diphos : dppm, dppe, dppp, dppb, dppf) or two moles equivalent of PPh3 afforded a complexes of the types [Hg(k1-ptt)2(diphos)] (2-6) or [Hg(k1-ptt)2(PPh3
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5

Wilson, Claire H., Hui Emma Zhang, Mark D. Gorrell, and Catherine A. Abbott. "Dipeptidyl peptidase 9 substrates and their discovery: current progress and the application of mass spectrometry-based approaches." Biological Chemistry 397, no. 9 (September 1, 2016): 837–56. http://dx.doi.org/10.1515/hsz-2016-0174.

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Abstract The enzyme members of the dipeptidyl peptidase 4 (DPP4) gene family have the very unusual capacity to cleave the post-proline bond to release dipeptides from the N-terminus of peptide/protein substrates. DPP4 and related enzymes are current and potential therapeutic targets in the treatment of type II diabetes, inflammatory conditions and cancer. Despite this, the precise biological function of individual dipeptidyl peptidases (DPPs), other than DPP4, and knowledge of their in vivo substrates remains largely unknown. For many years, identification of physiological DPP substrates has b
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6

Liang, Xi-Ling, and Li-Feng Tan. "Nucleic Acid (Calf Thymus-DNA, Yeast tRNA) Binding and Cytotoxic Properties of a Dinuclear (Ru,Co) Metal Polypyridyl Complex." Australian Journal of Chemistry 63, no. 10 (2010): 1453. http://dx.doi.org/10.1071/ch10178.

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Based on [L2Ru{DPPZ(11–11′)DPPZ}RuL2]4+ (where L = 1,10-phenanthroline or 2,2′-bipyridyl, DPPZ(11–11′)DPPZ = 11,11′-bi(dipyrido-[3,2-a:2′,3′-c]-phenazinyl)), a heterodinuclear (Ru,Co) metal polypyridyl complex [(phen)2Ru{DPPZ(11–11′)DPPZ}Co(phen)2]5+ (phen = 1,10-phenanthroline) has been designed and synthesized. A comparative study on the interaction of the complex with calf thymus DNA and yeast tRNA was investigated by UV-visible spectroscopy, fluorescence spectroscopy and viscosity measurements, as well as equilibrium dialysis and circular dichroism. The antitumour activities of the complex
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7

Di Pietro, Maria Letizia, Giuseppina La Ganga, Francesco Nastasi, and Fausto Puntoriero. "Ru(II)-Dppz Derivatives and Their Interactions with DNA: Thirty Years and Counting." Applied Sciences 11, no. 7 (March 29, 2021): 3038. http://dx.doi.org/10.3390/app11073038.

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Transition metal complexes with dppz-type ligands (dppz = dipyrido[3,2-a:2′,3′-c]phenazine) are extensively studied and attract a considerable amount of attention, becoming, from the very beginning and increasingly over time, a powerful tool for investigating the structure of the DNA helix. In particular, [Ru(bpy)2(dppz)]2+ and [Ru(phen)2(dppz)]2+ and their derivatives were extensively investigated as DNA light-switches. The purpose of this mini-review, which is not and could not be exhaustive, was to first introduce DNA and its importance at a biological level and research in the field of sma
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8

Shahabadi, Nahid, and Maryam Mahdavi. "DNA Interaction Studies of a Cobalt(II) Mixed-Ligand Complex Containing Two Intercalating Ligands: 4,7-Dimethyl-1, 10-Phenanthroline and Dipyrido[3,2-a:2′,3′-c]phenazine." ISRN Inorganic Chemistry 2013 (December 30, 2013): 1–7. http://dx.doi.org/10.1155/2013/604218.

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A new cobalt(II) complex [Co(dppz)2(4,7-dmp)]2+ (4,7-dmp = 4,7-dimethyl-1,10-phenanthrolline) and dppz = dipyrido[3,2-a:2′-3′-c]phenazine has been synthesized and characterized by elemental analysis (CHN), FT-IR, and UV-visible (UV-Vis) spectroscopic techniques. The DNA-binding property of the complex has been investigated employing absorption spectroscopy, fluorescence spectroscopy, circular dichroism, and viscosity measurements. The experimental results show that the complex can bind to DNA in an intercalation mode. In comparison with previous study, the DNA-binding affinity of [Co(dppz)2(4,
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9

He, Xiaojun, Lianhe Jin, and Lifeng Tan. "DNA-binding, topoisomerases I and II inhibition and in vitro cytotoxicity of ruthenium(II) polypyridyl complexes: [Ru(dppz)2L]2+ (L=dppz-11-CO2Me and dppz)." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 135 (January 2015): 101–9. http://dx.doi.org/10.1016/j.saa.2014.06.147.

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10

Rochford, Garret, Zara Molphy, Kevin Kavanagh, Malachy McCann, Michael Devereux, Andrew Kellett, and Orla Howe. "Cu(ii) phenanthroline–phenazine complexes dysregulate mitochondrial function and stimulate apoptosis." Metallomics 12, no. 1 (2020): 65–78. http://dx.doi.org/10.1039/c9mt00187e.

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Herein we report the central role of the mitochondria in the cytotoxicity of four developmental cytotoxic copper(ii) complexes [Cu(phen)<sub>2</sub>]<sup>2+</sup>, [Cu(DPQ)(Phen)]<sup>2+</sup>, [Cu(DPPZ)(Phen)]<sup>2+</sup> and [Cu(DPPN)(Phen)]<sup>2+</sup> superior to cisplatin and independent of resistance in a range of cells.
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11

Smith, Jr., Dale C., Jérémie Cadoret, Laleh Jafarpour, Edwin D. Stevens, and Steven P. Nolan. "Synthetic and solution calorimetric investigations of chelating phosphine ligands in Ru(allyl)2(PP) complexes (PP = diphosphine)." Canadian Journal of Chemistry 79, no. 5-6 (May 1, 2001): 626–31. http://dx.doi.org/10.1139/v00-164.

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Reaction enthalpies of (COD)Ru(allyl)2 (COD = η4-1,5-cyclooctadiene; allyl = 2-methylpropenyl) with a series of bidentate phosphines (dppm, dppf, dppe, dppb, dppp, depe, dmpe) have been measured by anaerobic solution calorimetry. The relative stability of the resulting complexes is strongly influenced by the electronic donor properties of the bidentate phosphine ligand. Reactions involving ligands that are better σP) donors result in higher enthalpy values and, therefore, more thermodynamically stable complexes. Additionally, the synthesis and characterization of two new ruthenium allyl comple
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12

Mårtensson, Anna K. F., and Per Lincoln. "Binding of Ru(terpyridine)(pyridine)dipyridophenazine to DNA studied with polarized spectroscopy and calorimetry." Dalton Transactions 44, no. 8 (2015): 3604–13. http://dx.doi.org/10.1039/c4dt02642j.

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Achiral Ru(tpy)(py)dppz<sup>2+</sup> intercalated into DNA has similar intermolecular interactions as opposite enantiomers of its structural isomer, the “light-switch” complex Ru(bpy)<sub>2</sub>dppz<sup>2+</sup>.
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13

Savić, Aleksandar, Anna M. Kaczmarek, Rik Van Deun, and Kristof Van Hecke. "DNA Intercalating Near-Infrared Luminescent Lanthanide Complexes Containing Dipyrido[3,2-a:2′,3′-c]phenazine (dppz) Ligands: Synthesis, Crystal Structures, Stability, Luminescence Properties and CT-DNA Interaction." Molecules 25, no. 22 (November 13, 2020): 5309. http://dx.doi.org/10.3390/molecules25225309.

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In order to create near-infrared (NIR) luminescent lanthanide complexes suitable for DNA-interaction, novel lanthanide dppz complexes with general formula [Ln(NO3)3(dppz)2] (Ln = Nd3+, Er3+ and Yb3+; dppz = dipyrido[3,2-a:2′,3′-c]phenazine) were synthesized, characterized and their luminescence properties were investigated. In addition, analogous compounds with other lanthanide ions (Ln = Ce3+, Pr3+, Sm3+, Eu3+, Tb3+, Dy3+, Ho3+, Tm3+, Lu3+) were prepared. All complexes were characterized by IR spectroscopy and elemental analysis. Single-crystal X-ray diffraction analysis of the complexes (Ln
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14

Chao, Xi-Juan, Miao Tang, Rong Huang, Chun-Hua Huang, Jie Shao, Zhu-Ying Yan, and Ben-Zhan Zhu. "Targeted live-cell nuclear delivery of the DNA ‘light-switching’ Ru(II) complex via ion-pairing with chlorophenolate counter-anions: the critical role of binding stability and lipophilicity of the ion-pairing complexes." Nucleic Acids Research 47, no. 20 (October 4, 2019): 10520–28. http://dx.doi.org/10.1093/nar/gkz152.

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Abstract We have found recently that nuclear uptake of the cell-impermeable DNA light-switching Ru(II)-polypyridyl cationic complexes such as [Ru(bpy)2(dppz)]Cl2 was remarkably enhanced by pentachlorophenol (PCP), by forming ion-pairing complexes via a passive diffusion mechanism. However, it is not clear whether the enhanced nuclear uptake of [Ru(bpy)2(dppz)]2+ is only limited to PCP, or it is a general phenomenon for other highly chlorinated phenols (HCPs); and if so, what are the major physicochemical factors in determining nuclear uptake? Here, we found that the nuclear uptake of [Ru(bpy)2
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15

Higgs, P. L., A. W. McKinley, and E. M. Tuite. "[Ru(phen)2dppz]2+ luminescence reveals nanoscale variation of polarity in the cyclodextrin cavity." Chemical Communications 52, no. 9 (2016): 1883–86. http://dx.doi.org/10.1039/c5cc09755j.

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Insertion of dppz with phosphorylated β-cyclodextrin results in multi-exponential [Ru(phen)<sub>2</sub>dppz]<sup>2+</sup> emission; binding is weaker than [Ru(phen)<sub>3</sub>]<sup>2+</sup>, but shows stereoselectivity.
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16

Wijaya, Karna, Daryono H. Tjahjono, Naoki Yoshioka, and Hidenari Inoue. "DNA-Binding Properties of Iron(II) Mixed-Ligand Complexes Containing 1,10-Phenanthroline and Dipyrido[3,2-a:2’,3’-c]phenazine." Zeitschrift für Naturforschung B 59, no. 3 (March 1, 2004): 310–18. http://dx.doi.org/10.1515/znb-2004-0313.

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An iron(II) mixed-ligand complex with 1,10-phenanthroline (phen) and dipyrido[3,2-a:2’,3’- c]phenazine (dppz), [Fe(phen)2(dppz)]2+, has been synthesized. The DNA-binding properties of the mixed-ligand complex have been studied in terms of equilibrium binding constant, thermodynamic parameter, thermal denaturation as well as Pfeiffer effect upon binding to DNA. The spectrophotometric titration of [Fe(phen)2(dppz)]2+ with calf thymus DNA (ct-DNA) has shown that the iron(II) mixed-ligand complex binds effectively to ct-DNA in an intercalation mode as indicated by remarkable hypochromicity (ca. 36
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Nagaraj, Karuppiah, Krishnan Senthil Murugan, Pilavadi Thangamuniyandi, and Subramanian Sakthinathan. "Nucleic acid binding study of surfactant copper(ii) complex containing dipyrido[3,2-a:2′-3′-c]phenazine ligand as an intercalator: in vitro antitumor activity of complex in human liver carcinoma (HepG2) cancer cells." RSC Adv. 4, no. 99 (2014): 56084–94. http://dx.doi.org/10.1039/c4ra08049a.

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A new surfactant copper(ii) complex, [Cu(dppz)<sub>2</sub>DA](ClO<sub>4</sub>)<sub>2</sub>, where dppz = dipyrido[3,2-a:2′-3′-c]phenazine and DA-dodecylamine, has been synthesized and characterized by physico-chemical and spectroscopic methods.
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Hall, James P., Hanna Beer, Katrin Buchner, David J. Cardin та Christine J. Cardin. "Preferred orientation in an angled intercalation site of a chloro-substituted Λ -[Ru(TAP) 2 (dppz)] 2+ complex bound to d(TCGGCGCCGA) 2". Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 371, № 1995 (28 липня 2013): 20120525. http://dx.doi.org/10.1098/rsta.2012.0525.

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The crystal structure of the ruthenium DNA ‘light-switch’ complex Λ -[Ru(TAP) 2 (11-Cl-dppz)] 2+ (TAP=tetraazaphenanthrene, dppz=dipyrido[3,2- a ′:2′,3′- c ]phenazine) bound to the oligonucleotide duplex d(TCGGCGCCGA) 2 is reported. The synthesis of the racemic ruthenium complex is described for the first time, and the racemate was used in this study. The crystal structure, at atomic resolution (1.0 Å), shows one ligand as a wedge in the minor groove, resulting in the 51 ° kinking of the double helix, as with the parent Λ -[Ru(TAP) 2 (dppz)] 2+ . Each complex binds to one duplex by intercalati
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19

Huang, Jiali Carrie, Abdullah Al Emran, Justine Moreno Endaya, Geoffrey W. McCaughan, Mark D. Gorrell, and Hui Emma Zhang. "DPP9: Comprehensive In Silico Analyses of Loss of Function Gene Variants and Associated Gene Expression Signatures in Human Hepatocellular Carcinoma." Cancers 13, no. 7 (April 1, 2021): 1637. http://dx.doi.org/10.3390/cancers13071637.

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Dipeptidyl peptidase (DPP) 9, DPP8, DPP4 and fibroblast activation protein (FAP) are the four enzymatically active members of the S9b protease family. Associations of DPP9 with human liver cancer, exonic single nucleotide polymorphisms (SNPs) in DPP9 and loss of function (LoF) variants have not been explored. Human genomic databases, including The Cancer Genome Atlas (TCGA), were interrogated to identify DPP9 LoF variants and associated cancers. Survival and gene signature analyses were performed on hepatocellular carcinoma (HCC) data. We found that DPP9 and DPP8 are intolerant to LoF variants
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Ross, Breyan, Stephan Krapp, Martin Augustin, Reiner Kierfersauer, Marcelino Arciniega, Ruth Geiss-Friedlander, and Robert Huber. "Structures and mechanism of dipeptidyl peptidases 8 and 9, important players in cellular homeostasis and cancer." Proceedings of the National Academy of Sciences 115, no. 7 (January 30, 2018): E1437—E1445. http://dx.doi.org/10.1073/pnas.1717565115.

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Dipeptidyl peptidases 8 and 9 are intracellular N-terminal dipeptidyl peptidases (preferentially postproline) associated with pathophysiological roles in immune response and cancer biology. While the DPP family member DPP4 is extensively characterized in molecular terms as a validated therapeutic target of type II diabetes, experimental 3D structures and ligand-/substrate-binding modes of DPP8 and DPP9 have not been reported. In this study we describe crystal and molecular structures of human DPP8 (2.5 Å) and DPP9 (3.0 Å) unliganded and complexed with a noncanonical substrate and a small molec
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Phillips, Tim, Ihtshamul Haq, Anthony J. H. M. Meijer, Harry Adams, Ian Soutar, Linda Swanson, Matthew J. Sykes, and Jim A. Thomas. "DNA Binding of an Organic dppz-Based Intercalator†." Biochemistry 43, no. 43 (November 2004): 13657–65. http://dx.doi.org/10.1021/bi049146r.

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Shi, Shuo, Jin-Hong Xu, Xing Gao, Hai-Liang Huang, and Tian-Ming Yao. "Binding Behaviors for Different Types of DNA G-Quadruplexes: Enantiomers of [Ru(bpy)2(L)]2+(L=dppz, dppz-idzo)." Chemistry - A European Journal 21, no. 32 (June 26, 2015): 11435–45. http://dx.doi.org/10.1002/chem.201501093.

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van der Salm, Holly, Christopher B. Larsen, James R. W. McLay, Michael G. Fraser, Nigel T. Lucas, and Keith C. Gordon. "Stretching the phenazine MO in dppz: the effect of phenyl and phenyl–ethynyl groups on the photophysics of Re(i) dppz complexes." Dalton Trans. 43, no. 47 (2014): 17775–85. http://dx.doi.org/10.1039/c4dt01415d.

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Bouzada, David, Iria Salvadó, Ghofrane Barka, Gustavo Rama, José Martínez-Costas, Romina Lorca, Álvaro Somoza, Manuel Melle-Franco, M. Eugenio Vázquez, and Miguel Vázquez López. "Selective G-quadruplex binding by oligoarginine-Ru(dppz) metallopeptides." Chemical Communications 54, no. 6 (2018): 658–61. http://dx.doi.org/10.1039/c7cc08286j.

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We demonstrate that both the R<sub>8</sub> functionalization and its interplay with the ancillary ligand have and an important role in the G-quadruplex recognition process by Ru(dppz) metallopeptides.
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Moncada, Alejandra Saavedra, Eduart Gutiérrez-Pineda, Iván Maisuls, Gustavo T. Ruiz, Alexander G. Lappin, Guillermo J. Ferraudi, and Ezequiel Wolcan. "Photochemical properties of a Re(I) polymer containing dppz in its structure. An interplay between dark and bright states of dppz." Journal of Photochemistry and Photobiology A: Chemistry 353 (February 2018): 86–100. http://dx.doi.org/10.1016/j.jphotochem.2017.11.007.

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Klein, Axel, Natascha Hurkes, André Kaiser та Wolfram Wielandt. "π-Stacking Modulates the Luminescence of [(dppz)Ni(Mes)Br] (dppz = dipyrido[3,2-a:2′,3′-c]phenazine, Mes = 2,4,6-trimethylphenyl)". Zeitschrift für anorganische und allgemeine Chemie 633, № 10 (серпень 2007): 1659–65. http://dx.doi.org/10.1002/zaac.200700082.

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Li, Guanying, Lingli Sun, Liangnian Ji, and Hui Chao. "Ruthenium(ii) complexes with dppz: from molecular photoswitch to biological applications." Dalton Transactions 45, no. 34 (2016): 13261–76. http://dx.doi.org/10.1039/c6dt01624c.

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The present article describes the recent advances in biological applications of the Ru-dppz systems in DNA binding, cellular imaging, anticancer drugs, phototherapy, protein aggregation detecting and chemosensors.
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van der Salm, Holly, Christopher B. Larsen, James R. W. McLay, Gregory S. Huff, and Keith C. Gordon. "Effects of protonation on the optical and photophysical properties of ReCl(CO)3(dppz–TAA) and [Ru(bpy)2(dppz–TAA)]2+." Inorganica Chimica Acta 428 (March 2015): 1–7. http://dx.doi.org/10.1016/j.ica.2015.01.006.

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Santos, Teresa M., João Madureira, Brian J. Goodfellow, Michael G. B. Drew, Júlio Pedrosa de Jesus, and Vitor Félix. "Interaction of Ruthenium(II)-dipyridophenazine Complexes with CT-DNA: Effects of the Polythioether Ancillary Ligands." Metal-Based Drugs 8, no. 3 (January 1, 2001): 125–36. http://dx.doi.org/10.1155/mbd.2001.125.

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The complexes [Ru([9]aneS3)(dppz)Cl]Cl 1 and [Ru([12]aneS4)(dppz)]Cl2,2 ([9]aneS3 = 1,4,7- trithiaciclononane and [12]aneS4 = 1,4,7,10-tetrathiaciclododecane) were synthesised and fully characterised . These complexes belong to a small family of dipyridophenazine complexes with non-polypyridyl ancillary ligands . Interaction studies of these complexes with CT-DNA (UV/Vis titrations, steady-state emission and thermal denaturation) revealed their high affinity for DNA . Intercalation constants determined by UV/Vis titrations are of the same order of magnitude (106) as other dppz metallointercala
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Coates, Colin G., John J. McGarvey, Steven E. J. Bell, Luc Jacquet, John M. Kelly, Tia Keyes, and Johannes G. Vos. "Transient Resonance Raman Studies of Ru(II) Complexes in DNA and in Homogeneous Media." Laser Chemistry 19, no. 1-4 (January 1, 1999): 237–43. http://dx.doi.org/10.1155/1999/74587.

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Transient resonance Raman (TR2) spectroscopy has been used to investigate the metalligand charge-transfer (MLCT) excited states of Ru(II) polypyridyl complexes inDNAand in homogeneous solution. In DNA, complexes of the type [Ru(L)2(L′)]2+ were studied, where L=2, 2’-bipyridyl (bpy), 1,4, 5, 8-tetraazaphenanthrene (tap), and L′ dipyrido [3,2:a-2′ ,3′:c]-phenazine (dppz) or 1,4,5,8,9,12-hexaazatriphenylene (HAT). For [Ru(bpy)2(HAT)]2+, the enhancement pattern of vibrational modes in the TR2 spectra attributable to reduced HAT⋅− in the triplet MLCT state suggest perturbations to the intraligand t
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31

Alsaedi, Sammar, Bandar A. Babgi, Magda H. Abdellattif, Muhammad N. Arshad, Abdul-Hamid M. Emwas, Mariusz Jaremko, Mark G. Humphrey, Abdullah M. Asiri, and Mostafa A. Hussien. "DNA-Binding and Cytotoxicity of Copper(I) Complexes Containing Functionalized Dipyridylphenazine Ligands." Pharmaceutics 13, no. 5 (May 20, 2021): 764. http://dx.doi.org/10.3390/pharmaceutics13050764.

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A set of copper(I) coordination compounds with general formula [CuBr(PPh3)(dppz-R)] (dppz-R = dipyrido[3,2-a:2’,3’-c]phenazine (Cu-1), 11-nitrodipyrido[3,2-a:2’,3’-c]phenazine (Cu-2), 11-cyanodipyrido[3,2-a:2’,3’-c]phenazine (Cu-3), dipyrido[3,2-a:2’,3’-c]phenazine-11-phenone (Cu-4), 11,12-dimethyldipyrido[3,2-a:2’,3’-c]phenazine (Cu-5)) have been prepared and characterized by elemental analysis, 1H-NMR and 31P-NMR spectroscopies as well as mass spectrometry. The structure of Cu-1 was confirmed by X-ray crystallography. The effect of incorporating different functional groups on the dppz ligand
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Coogan, M. P., and J. A. Platts. "Blue rhenium tricarbonyl DPPZ complexes – low energy charge-transfer absorption at tissue-penetrating wavelengths." Chemical Communications 52, no. 84 (2016): 12498–501. http://dx.doi.org/10.1039/c6cc07125b.

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Chen, Xiangke, Zishuai Huang, Wei Hua, Hardy Castada, and Heather C. Allen. "Reorganization and Caging of DPPC, DPPE, DPPG, and DPPS Monolayers Caused by Dimethylsulfoxide Observed Using Brewster Angle Microscopy." Langmuir 26, no. 24 (December 21, 2010): 18902–8. http://dx.doi.org/10.1021/la102842a.

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Kawano, Hiroyuki, Rie Tanaka, Tomoko Fujikawa, Katsuma Hiraki, and Masayoshi Onishi. "Novel Dihydridoruthenium(II) Complexes with Chelating Diphosphine Ligands, RuH2(CO)(diphosphine)(PPh3) (diphosphine = dppe, dppp, dppb, and dppf)." Chemistry Letters 28, no. 5 (May 1999): 401–2. http://dx.doi.org/10.1246/cl.1999.401.

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Roy, Nilmadhab, Utsav Sen, Shreya Ray Chaudhuri, Venkatesan Muthukumar, Prithvi Moharana, Priyankar Paira, Bipasha Bose, Ashna Gauthaman, and Anbalagan Moorthy. "Mitochondria specific highly cytoselective iridium(iii)–Cp* dipyridophenazine (dppz) complexes as cancer cell imaging agents." Dalton Transactions 50, no. 6 (2021): 2268–83. http://dx.doi.org/10.1039/d0dt03586f.

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Liu, Xue-Wen, Jun Li, Hong Li, Kang-Cheng Zheng, Hui Chao, and Liang-Nian Ji. "Synthesis, characterization, DNA-binding and photocleavage of complexes [Ru(phen)2(6-OH-dppz)]2+ and [Ru(phen)2(6-NO2-dppz)]2+." Journal of Inorganic Biochemistry 99, no. 12 (December 2005): 2372–80. http://dx.doi.org/10.1016/j.jinorgbio.2005.09.004.

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McQuaid, Kane, James P. Hall, Lena Baumgaertner, David J. Cardin та Christine J. Cardin. "Three thymine/adenine binding modes of the ruthenium complex Λ-[Ru(TAP)2(dppz)]2+ to the G-quadruplex forming sequence d(TAGGGTT) shown by X-ray crystallography". Chemical Communications 55, № 62 (2019): 9116–19. http://dx.doi.org/10.1039/c9cc04316k.

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Liu, Clive, Patricia Marshall, Ian Schreibman, Ann Vu, Weiming Gai, and Michael Whitlow. "Interaction Between Terminal Complement Proteins C5b-7 and Anionic Phospholipids." Blood 93, no. 7 (April 1, 1999): 2297–301. http://dx.doi.org/10.1182/blood.v93.7.2297.407k19_2297_2301.

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We have recently shown that C5b-6 binds to the erythrocyte membrane via an ionic interaction with sialic acid before the addition of C7 and subsequent membrane insertion. In this study we assessed the role of anionic lipids in the binding of the terminal complement proteins to the membrane and the efficiency of subsequent hemolysis. Human erythrocytes were modified by insertion of dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phosphatidylserine (DPPS), dipalmitoyl phosphatidylethanolamine (DPPE), or dipalmitoyl phosphatidic acid (DPPA). Lipid incorporation and the hemolytic assays were d
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39

Kuhnt, Christian, Michael Karnahl, Stefanie Tschierlei, Kristin Griebenow, Michael Schmitt, Bernhard Schäfer, Sven Krieck, et al. "Substitution-controlled ultrafast excited-state processes in Ru–dppz-derivatives." Phys. Chem. Chem. Phys. 12, no. 6 (2010): 1357–68. http://dx.doi.org/10.1039/b915770k.

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Bates, W. Doug, Pingyun Chen, Dana M. Dattelbaum, Wayne E. Jones, and Thomas J. Meyer. "Excited State Competition infac-[ReI(dppz)(CO)3(py-PTZ)]+." Journal of Physical Chemistry A 103, no. 27 (July 1999): 5227–31. http://dx.doi.org/10.1021/jp990543z.

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Holmlin, R. Erik, and Jacqueline K. Barton. "Os(phen)2(dppz)2+: A Red-Emitting DNA Probe." Inorganic Chemistry 34, no. 1 (January 1995): 7–8. http://dx.doi.org/10.1021/ic00105a004.

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Yu, Hui-juan, Jiang-ping Liu, Zhi-feng Hao, Jun He, Ming Sun, Sheng Hu, Lin Yu, and Hui Chao. "Synthesis, characterization and biological evaluation of ruthenium(II) complexes [Ru(dtzp)(dppz)Cl] + and [Ru(dtzp)(dppz)CH 3 CN] 2+ for photodynamic therapy." Dyes and Pigments 136 (January 2017): 416–26. http://dx.doi.org/10.1016/j.dyepig.2016.08.059.

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Gao, Xing, Shuo Shi, Jun-Liang Yao, Juan Zhao, and Tian-Ming Yao. "Impacts of terminal modification of [Ru(phen)2dppz]2+on the luminescence properties: a theoretical study." Dalton Transactions 44, no. 44 (2015): 19264–74. http://dx.doi.org/10.1039/c5dt03373j.

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Hayashi, Yuichiro, Ami Morimoto, Takeshi Maeda, Toshiaki Enoki, Yousuke Ooyama, Yasunori Matsui, Hiroshi Ikeda та Shigeyuki Yagi. "Synthesis of novel π-extended D–A–D-type dipyrido[3,2-a:2′,3′-c]phenazine derivatives and their photosensitized singlet oxygen generation". New Journal of Chemistry 45, № 4 (2021): 2264–75. http://dx.doi.org/10.1039/d0nj05526c.

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Chengke, Wu, An Xiaoyu, Yue yuanyuan Yue yuanyuan, Feng Suling, and Niu Xiaoqing. "Effect of polypyridine copper complex [Cu(dppz)(l-Ser)]NO3·H2O on the stabilization of triplex DNA based on gold-nanoparticles." Analytical Methods 7, no. 8 (2015): 3425–30. http://dx.doi.org/10.1039/c5ay00139k.

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Schoch, Thomas K., John L. Hubbard, Christopher R. Zoch, Geun-Bae Yi та Morten Sørlie. "Synthesis and Structure of the Ruthenium(II) Complexes [(η-C5Me5)Ru(NO)(bipy)]2+and [(η-C5Me5)Ru(NO)(dppz)]2+. DNA Cleavage by an Organometallic dppz Complex (bipy = 2,2‘-Bipyridine; dppz = Dipyrido[3,2-a:2‘,3‘-c]phenazine)". Inorganic Chemistry 35, № 15 (січень 1996): 4383–90. http://dx.doi.org/10.1021/ic950743z.

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Devereux, Stephen J., Páraic M. Keane, Suni Vasudevan, Igor V. Sazanovich, Michael Towrie, Qian Cao, Xue-Zhong Sun, et al. "Study of picosecond processes of an intercalated dipyridophenazine Cr(iii) complex bound to defined sequence DNAs using transient absorption and time-resolved infrared methods." Dalton Trans. 43, no. 47 (2014): 17606–9. http://dx.doi.org/10.1039/c4dt01989j.

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Sun, Weize, Rena Boerhan, Na Tian, Yang Feng, Jian Lu, Xuesong Wang, and Qianxiong Zhou. "Fluorination in enhancing photoactivated antibacterial activity of Ru(ii) complexes with photo-labile ligands." RSC Advances 10, no. 42 (2020): 25364–69. http://dx.doi.org/10.1039/d0ra01806f.

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Fluorination in the dppz ligand efficiently enhanced the photoactivated antibacterial activity of Ru(ii) complexes with photo-labile ligands against antibiotic-resistant bacteria both under normoxic and hypoxic conditions.
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49

Liu, Clive, Patricia Marshall, Ian Schreibman, Ann Vu, Weiming Gai, and Michael Whitlow. "Interaction Between Terminal Complement Proteins C5b-7 and Anionic Phospholipids." Blood 93, no. 7 (April 1, 1999): 2297–301. http://dx.doi.org/10.1182/blood.v93.7.2297.

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Abstract We have recently shown that C5b-6 binds to the erythrocyte membrane via an ionic interaction with sialic acid before the addition of C7 and subsequent membrane insertion. In this study we assessed the role of anionic lipids in the binding of the terminal complement proteins to the membrane and the efficiency of subsequent hemolysis. Human erythrocytes were modified by insertion of dipalmitoyl phosphatidylcholine (DPPC), dipalmitoyl phosphatidylserine (DPPS), dipalmitoyl phosphatidylethanolamine (DPPE), or dipalmitoyl phosphatidic acid (DPPA). Lipid incorporation and the hemolytic assa
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50

Liu, Guocheng, Shuang Liang, Qiaomin Li, Jiao Guo, Na Xu, Xiuli Wang, Yan Li, and Baokuan Chen. "Metal/N-donor-induced versatile structures and properties of seven 0D → 3D complexes based on dpq/dppz and O-bridged tricarboxylate: fluorescence and electrochemical behaviors." CrystEngComm 22, no. 7 (2020): 1209–19. http://dx.doi.org/10.1039/c9ce01878f.

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Seven 0D → 3D coordination polymers based on dpq/dppz and O-bridged tricarboxylates have been hydrothermally synthesized and structurally directed by metal ions, which show different electrochemical and fluorescence behaviors.
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