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1. Phenazines [by] G.A. Swan [and] D.G.I. Felton
by Swan, G. A. 1917- (George Albert) and Felton, Desmond Geoffrey Ivins
1957, The Chemistry of heterocyclic compounds, v. 11, xix, 693 p. illus.
Phenazines
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2. Full Text One-pot, sequential four-component synthesis of benzo[c]pyrano[3,2-a]phenazine, bis-benzo[c]pyrano[3,2-a]phenazine and oxospiro benzo[c]pyrano[3,2-a]phenazine derivatives using 1,4-diazabicyclo[2.2.2]octane (DABCO) as an efficient and reusable solid base catalyst
by Hasaninejad, Alireza and Firoozi, Somayeh
Molecular Diversity, ISSN 1381-1991, 8/2013, Volume 17, Issue 3, pp. 499 - 513
1,4-Diazabicyclo[2.2.2]octane (DABCO) has been used as an efficient and reusable solid base catalyst for the one-pot, two-step, four-component synthesis of... 
Biochemistry, general | Multi-component reactions | Oxospiro benzo[ $$c$$ c ]pyrano[3 $$, $$ , 2- a ]phenazines | Bis- benzo[ $$c$$ c ]pyrano[3 $$, $$ , 2- a ]phenazines | DABCO | Life Sciences | Polymer Sciences | MCRs | Pyrano[3 $$, $$ , 2- a ]phenazines | Pharmacy | Microwave irradiation | 1 $$, $$ , 4-Diazabicyclooctane | Organic Chemistry | Pyrano[3, 2-a]phenazines | Bis- benzo[c]pyrano[3, 2-a]phenazines | 1, 4-Diazabicyclo[2.2.2]octane | Oxospiro benzo[c]pyrano[3, 2-a]phenazines | CHEMISTRY, MEDICINAL | ACID | ANALOGS | ANTICANCER AGENTS | NATURAL-PRODUCTS | 1,4-Diazabicyclo[2.2.2]octane | CHEMISTRY, MULTIDISCIPLINARY | HIGHLY EFFICIENT | BETA-LAPACHONE | SOLVENT-FREE | Oxospiro benzo[c]pyrano[3,2-a]phenazines | CHEMISTRY, APPLIED | Pyrano[3,2-a]phenazines | Bis- benzo[c]pyrano[3,2-a]phenazines | Phenazines - metabolism | Phenazines - chemistry | Drug Design | Molecular Structure | Piperazines - chemistry | Catalysis | Phenazines - chemical synthesis | Heterocyclic compounds
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3. Phenazines
by Swan, G. A and Felton, D. G. I
1957, Volume 11., xix, 693
Phenazines
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4. Full Text Recent developments in the isolation, biological function, biosynthesis, and synthesis of phenazine natural products
by Guttenberger, Nikolaus and Blankenfeldt, Wulf and Breinbauer, Rolf
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 11/2017, Volume 25, Issue 22, pp. 6149 - 6166
Phenazines are natural products which are produced by bacteria or by archaeal species. The tricyclic ring system enables redox processes, which producing... 
Biofilm | Natural product | Phenazine | Biosynthesis | Antibiotics | Anticancer | AIRWAY EPITHELIAL-CELLS | CHEMISTRY, MEDICINAL | ONE-POT SYNTHESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | PSEUDOMONAS-AERUGINOSA PYOCYANIN | CHEMISTRY, ORGANIC | 4-COMPONENT DOMINO PROTOCOL | TETRAMETHYLPIPERIDINE-SUBSTITUTED PHENAZINES | STREPTOMYCES SP | MULTIDRUG-RESISTANT TUBERCULOSIS | KITASATOSPORA SP MBT66 | N BOND FORMATION | PHENAZINE-1-CARBOXYLIC ACID | Biofilms - drug effects | Cell Survival - drug effects | Bacteria - metabolism | Bacteria - chemistry | Phenazines - pharmacology | Antineoplastic Agents - chemical synthesis | Humans | Archaea - chemistry | Biological Products - pharmacology | Pseudomonas aeruginosa - physiology | Antineoplastic Agents - chemistry | Biological Products - isolation & purification | Antineoplastic Agents - metabolism | Archaea - metabolism | Biological Products - chemistry | Animals | Phenazines - metabolism | Phenazines - chemistry | Biological Products - metabolism | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Anthranilate Synthase - metabolism | Phenazines - isolation & purification | Proteins | Chemical synthesis
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5. Full Text Phenazine containing indeno-furan based colorimetric and "on-off" fluorescent sensor for the detection of Cu 2+ and Pb 2
by Aggarwal, Komal and Khurana, Jitender M
Journal of Luminescence, ISSN 0022-2313, 07/2015, Volume 167, pp. 146 - 155
A new fluorescent sensor 10a,15a-dihydroxy-10aH-benzo[a]indeno[2′,1′:4,5]furo[2,3-c]phenazin-15(15aH)-one (1) based on the combination of phenazine and... 
Phenazine | Absorbance | Fluorescence | Indenofuran
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6. Full Text Phenazine-1-carboxylic acid and soil moisture influence biofilm development and turnover of rhizobacterial biomass on wheat root surfaces: PCA and soil moisture impact biofilm development
by LeTourneau, Melissa K and Marshall, Matthew J and Cliff, John B and Bonsall, Robert F and Dohnalkova, Alice C and Mavrodi, Dmitri V and Devi, S. Indira and Mavrodi, Olga V and Harsh, James B and Weller, David M and Thomashow, Linda S and Pacific Northwest National Lab. (PNNL), Richland, WA (United States)
Environmental Microbiology, ISSN 1462-2912, 06/2018, Volume 20, Issue 6
Phenazine-1-carboxylic acid (PCA) is produced by rhizobacteria in dryland but not in irrigated wheat fields of the Pacific Northwest, USA. PCA promotes biofilm... 
Phenazine, biofilm, wheat
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7. Full Text Simple synthesis of endophenazine G and other phenazines and their evaluation as anti-methicillin-resistant Staphylococcus aureus agents
by Udumula, Venkatareddy and Endres, Jennifer L and Harper, Caleb N and Jaramillo, Lee and Zhong, Haizhen A and Bayles, Kenneth W and Conda-Sheridan, Martin
European Journal of Medicinal Chemistry, ISSN 0223-5234, 01/2017, Volume 125, pp. 710 - 721
Community-associated methicillin resistant (CA-MRSA) has become a severe health concern because of its treatment difficulties. Herein, we report the synthesis... 
Antibacterial Agents | Natural Product Synthesis | Bacterial Infections | MRSA | Methicillin-Resistant Staphylococcus Aureus | Drug-resistant Bacteria | Phenazines | MYCOBACTERIUM-TUBERCULOSIS | CELLS | CHEMISTRY, MEDICINAL | HALOGENATED PHENAZINES | BIOFILMS | SUBSTITUTED PHENAZINES | DISCOVERY | THERAPY | ANTIMICROBIAL ACTIVITY | Phthalazines - chemical synthesis | Phenazines - pharmacology | Methicillin-Resistant Staphylococcus aureus - drug effects | Phthalazines - chemistry | Anti-Bacterial Agents - chemical synthesis | Microbial Sensitivity Tests | Phthalazines - pharmacology | Phenazines - chemistry | Anti-Bacterial Agents - chemistry | Inhibitory Concentration 50 | Anti-Bacterial Agents - pharmacology | Molecular Structure | Phenazines - chemical synthesis | Quantitative Structure-Activity Relationship | Drug resistance in microorganisms | Analysis | Staphylococcus aureus | Staphylococcus aureus infections
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8. Full Text Total synthesis and antileukemic evaluations of the phenazine 5,10-dioxide natural products iodinin, myxin and their derivatives
by Viktorsson, Elvar Örn and Melling Grøthe, Bendik and Aesoy, Reidun and Sabir, Misbah and Snellingen, Simen and Prandina, Anthony and Høgmoen Åstrand, Ove Alexander and Bonge-Hansen, Tore and Døskeland, Stein Ove and Herfindal, Lars and Rongved, Pål
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 04/2017, Volume 25, Issue 7, pp. 2285 - 2293
A new efficient total synthesis of the phenazine 5,10-dioxide natural products iodinin and myxin and new compounds derived from them was achieved in few steps,... 
Phenazine 5,10-dioxides | Hypoxia selectivity | Acute myeloid leukemia | Phenazines | CHEMISTRY, MEDICINAL | BIOCHEMISTRY & MOLECULAR BIOLOGY | BONE-MARROW | CHEMISTRY, ORGANIC | TIRAPAZAMINE | ACUTE MYELOID-LEUKEMIA | CELL-LINES | HYPOXIA | DAUNORUBICIN | CANCER | CISPLATIN | BIOSYNTHESIS | RIBONUCLEIC-ACID SYNTHESIS | Biological Products - chemical synthesis | Phenazines - pharmacology | Phenazines - chemistry | Humans | Cell Line, Tumor | Biological Products - pharmacology | Structure-Activity Relationship | Phenazines - chemical synthesis | Synthesis | Organic compounds | Drugstores | Cell death | Pharmacy | Leukemia
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9. Full Text An optical and electrical study of full thermally activated delayed fluorescent white organic light-emitting diodes
by Pereira, Daniel De Sa and Dos Santos, Paloma L and Ward, Jonathan S and Data, Przemyslaw and Okazaki, Masato and Takeda, Youhei and Minakata, Satoshi and Bryce, Martin R and Monkman, Andrew P
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 6234 - 8
We report on the engineering of full thermally activated delayed fluorescence - based white organic light emitting diodes (W-OLEDs) composed of three emitters... 
Organic light emitting diodes | Phenazine
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10. Full Text Finely Tuned Temperature‐Controlled Cargo Release Using Paraffin‐Capped Mesoporous Silica Nanoparticles
by Aznar, Elena and Mondragón, Laura and Ros‐Lis, José V and Sancenón, Félix and Marcos, M. Dolores and Martínez‐Máñez, Ramón and Soto, Juan and Pérez‐Payá, Enrique and Amorós, Pedro
Angewandte Chemie International Edition, ISSN 1433-7851, 11/2011, Volume 50, Issue 47, pp. 11172 - 11175
Trapped: Mesoporous silica nanoparticles were loaded with a fluorescent guest and functionalized with octadecyltrimethoxysilane. The alkyl chains interact with... 
molecular gates | controlled release | nanoparticles | drug delivery | mesoporous materials | SYSTEM | SACCHARIDES | DESIGN | DRUG-DELIVERY | GUEST MOLECULES | SUPPORTS | DRIVEN | CHEMISTRY, MULTIDISCIPLINARY | RESPONSIVE CONTROLLED-RELEASE | TRANSPORT | SCAFFOLDINGS | Cell Survival - drug effects | Microscopy, Electron, Transmission | Temperature | Phenazines - pharmacology | Nanoparticles - chemistry | Humans | Silicon Dioxide - chemistry | Solubility | Models, Molecular | Paraffin - chemistry | Doxorubicin - chemistry | Antineoplastic Agents - chemistry | Drug Carriers - chemistry | Microscopy, Confocal | Phenazines - chemistry | X-Ray Diffraction | Surface Properties | Antineoplastic Agents - pharmacology | Molecular Structure | HeLa Cells | Porosity | Delayed-Action Preparations | Doxorubicin - pharmacology
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11. Full Text Phenazine containing indeno-furan based colorimetric and “on–off” fluorescent sensor for the detection of Cu2+ and Pb2
by Aggarwal, Komal and Khurana, Jitender M
Journal of Luminescence, ISSN 0022-2313, 11/2015, Volume 167, pp. 146 - 155
A new fluorescent sensor 10 ,15 -dihydroxy-10 -benzo[ ]indeno[2′,1′:4,5]furo[2,3- ]phenazin-15(15 )-one ( ) based on the combination of phenazine and... 
Phenazine | Absorbance | Fluorescence | Indenofuran
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12. Full Text A comparative investigation of dibenzo[a,c]phenazine and quinoxaline donor–acceptor conjugated polymers: Correlation of planar structure and intramolecular charge transfer properties
by Kim, Doo Hun and Han, Yong Woon and Moon, Doo Kyung
Polymer, ISSN 0032-3861, 10/2019, p. 121906
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13. Full Text Multicomponent Synthesis of Poly-Substituted Benzo[a]pyrano[2,3-c]phenazine Derivatives under Microwave Heating
by Wang, Shu-Liang and Wu, Fei-Yue and Cheng, Chuang and Zhang, Ge and Liu, Yin-Ping and Jiang, Bo and Shi, Feng and Tu, Shu-Jiang
ACS Combinatorial Science, ISSN 2156-8952, 03/2011, Volume 13, Issue 2, pp. 135 - 139
A new one-pot two-step tandem synthesis of highly functionalized benzo[a]pyrano[2,3-c]phenazine derivatives via microwave-assisted multicomponent reactions of... 
4-dione | Multicomponent reactions | Tandem synthesis | Microwave heating | 2-hydroxynaphthalene-1 | Benzo[a]pyrano[2,3-c] phenazine | multicomponent reactions | CHEMISTRY, MEDICINAL | ANALOGS | ANTICANCER AGENTS | NATURAL-PRODUCTS | PHENAZINES | DRUG DISCOVERY | benzo[a]pyrano[2,3-c]phenazine | CHEMISTRY, MULTIDISCIPLINARY | tandem synthesis | microwave heating | IRRADIATION | DIVERSITY-ORIENTED SYNTHESIS | 2-hydroxynaphthalene-1,4-dione | BIOLOGICAL-ACTIVITY | CHEMISTRY | INHIBITORS | CHEMISTRY, APPLIED | Combinatorial Chemistry Techniques - methods | Phenazines - chemistry | Heating | Pyrans - chemistry | Enzyme Inhibitors - chemistry | Crystallography, X-Ray | Molecular Structure | Phenazines - chemical synthesis | Enzyme Inhibitors - chemical synthesis | Microwaves
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14. Full Text Genome-based discovery of a novel membrane-bound 1,6-dihydroxyphenazine prenyltransferase from a marine actinomycete
by Zeyhle, Philipp and Bauer, Judith S and Kalinowski, Jörn and Shin-ya, Kazuo and Gross, Harald and Heide, Lutz
PLoS ONE, ISSN 1932-6203, 06/2014, Volume 9, Issue 6, p. e99122
Recently, novel prenylated derivatives of 1,6-dihydroxyphenazine have been isolated from the marine sponge-associated Streptomyces sp. SpC080624SC-11. Genome... 
SYNTHASE | BIOSYNTHETIC GENE-CLUSTER | NATURAL-PRODUCTS | PSEUDOMONAS | PRENYLATION | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI | PHENAZINE BIOSYNTHESIS | MEVALONATE PATHWAY | HETEROLOGOUS EXPRESSION | ISOPRENOID PRODUCTION | Prenylation | Genome, Bacterial | Multigene Family | Recombinant Proteins - chemistry | Substrate Specificity | Recombinant Proteins - genetics | Chromatography, High Pressure Liquid | Recombinant Proteins - biosynthesis | Sequence Analysis, DNA | Phenazines - metabolism | Dimethylallyltranstransferase - genetics | Phenazines - chemistry | Mass Spectrometry | Actinobacteria - genetics | Cloning, Molecular | Escherichia coli - metabolism | Dimethylallyltranstransferase - metabolism | Phenazines - analysis | Kinetics | Dimethylallyltranstransferase - chemistry | Physiological aspects | Enzymes | Genomes | Escherichia coli | Genomics | Plant metabolites | Cytochrome | Similarity | Prenyltransferases | Laboratories | Genes | Cloning | Biosynthesis | Gene expression | Substrates | Gene sequencing | Proteins | Phenazine | Microorganisms | Secondary metabolites | Ubiquinone | Metabolites | E coli | Clusters
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15. Full Text 3-Chloro-4-hydroxyphenylacetic acid co-crystals with nicotinamide, isonicotinamide, phenazine and 4,4′-bipyridine: An investigation of synthon motifs
by Ngoma Tchibouanga, Remi Rolland and Jacobs, Ayesha
Journal of Molecular Structure, ISSN 0022-2860, 03/2020, Volume 1204, p. 127195
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16. Full Text Phenazines and cancer
by Cimmino, A and Evidente, A and Mathieu, V and Andolfi, A and Lefranc, F and Kornienko, A and Kiss, R
Natural Product Reports, ISSN 0265-0568, 4/2012, Volume 29, Issue 4, pp. 487 - 51
Covering: 2000 to 2011 Phenazines are a large group of natural and synthesised nitrogen-containing heterocycles, including more than 100 different compounds of... 
CHEMISTRY, MEDICINAL | POTENTIAL ANTITUMOR AGENTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CYTOTOXICITY EVALUATION | CHEMISTRY, ORGANIC | TOPOISOMERASE-I | PD 116,152 | IN-VITRO | STREPTOMYCES-ANTIBIOTICUS | BIOSYNTHESIS | XR5944 | PHASE-I | SYNTHETIC ANALOGS | Phenazines - pharmacology | Phenazines - chemistry | Antineoplastic Agents - isolation & purification | Antineoplastic Agents - chemical synthesis | Humans | Antineoplastic Agents - pharmacology | Molecular Structure | Phenazines - chemical synthesis | Antineoplastic Agents - chemistry | Phenazines - isolation & purification
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17. Full Text Structural modifications on the phenazine N, N′-dioxide-scaffold looking for new selective hypoxic cytotoxins
by Lavaggi, María Laura and Nieves, Marcos and Cabrera, Mauricio and Olea-Azar, Claudio and López de Ceráin, Adela and Monge, Antonio and Cerecetto, Hugo and González, Mercedes
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2010, Volume 45, Issue 11, pp. 5362 - 5369
We have identified phenazine 5,10-dioxides as prodrugs for antitumour therapy that undergo hypoxic-selective bioreduction to form cytotoxic species. Here, we... 
Phenazine N, N′-dioxides | Bioreductive agents | Cancer | Phenazine N,N′-dioxides | CHEMISTRY, MEDICINAL | Phenazine N,N '-dioxides | NEUTRAL RED | DRUGS | AGENTS | BINDING | N-OXIDE DERIVATIVES | CALF THYMUS DNA | Cell Line | Cricetinae | Animals | Cytotoxins - pharmacology | Phenazines - pharmacology | Spectrometry, Mass, Electrospray Ionization | Magnetic Resonance Spectroscopy | Phenazines - chemistry | Cytotoxins - chemistry | Electrochemistry | Hypoxia | Molecular Structure | Fluorescence | Cell research | Index Medicus
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18. Full Text Front Cover: Synthesis of π‐Functional Molecules through Oxidation of Aromatic Amines (Chem. Asian J. 15/2019)
by Hiroto, Satoru
Chemistry – An Asian Journal, ISSN 1861-4728, 08/2019, Volume 14, Issue 15, pp. 2512 - 2512
Oxidation of aromatic amines has been a powerful tool for connecting π‐conjugated molecules. Originating from aniline oxidation, a variety of reactions and... 
oxidation | azobenzene | phenazine | aniline | π-conjugated molecules
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19. Full Text Improved antileishmanial activity of dppz through complexation with antimony(III) and bismuth(III): Investigation of the role of the metal
by Lizarazo-Jaimes, Edgar H and Monte-Neto, Rubens L and Reis, Priscila G and Fernandes, Nelson G and Speziali, Nivaldo L and Melo, Maria N and Frézard, Frédéric and Demicheli, Cynthia
Molecules, ISSN 1420-3049, 11/2012, Volume 17, Issue 11, pp. 12622 - 12635
Two novel trivalent antimony(III) and bismuth(III) complexes with the nitrogen-donor heterocyclic ligand dipyrido[3,2-a:2',3'-c]phenazine (dppz) were... 
Bismuth | Dipyrido [3,2-a:2′,3′-c] phenazine | Antimony | Drug resistance | Leishmania | Crystal structure | antimony | BIOCHEMISTRY & MOLECULAR BIOLOGY |