Relevant bibliographies by topics / Phenoxazine derivatives

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Phenoxazine derivatives'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Phenoxazine derivatives.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Phenoxazine derivatives"

1

Journal, Baghdad Science. "Synthesis of New N-Substituted Phenoxazine Derivatives." Baghdad Science Journal 13, no. 2 (2016): 360–65. http://dx.doi.org/10.21123/bsj.13.2.360-365.

Full text
Abstract:
This work comprises the synthesis of new phenoxazine derivatives containing N-substituted phenoxazine starting from phenoxazine (1). Synthesis of ethyl acetate phenoxazine (2) through the reaction of phenoxazine with ethylchloroacetate, which reacted with hydrazine hydrate to give 10-aceto hydrazide phenoxazine (3), then reacted with formic acid to give 10-[N-formyl acetohydrazide] phenoxazine (4). Reaction of compound (4) with phosphorous pentaoxide or phosphorus pentasulphide to gave 10-[N-methylene-1,3,4-oxadiazole] phenoxazine (5) and 10-[N-methylene-1,3,4-thiadiazole] phenoxazine (6).
APA, Harvard, Vancouver, ISO, and other styles
2

Hu, Bin, Haizeng Song, Xinlei Zhang, Yuan He, Jingshun Ren, and Jingbin Huang. "Effects of Phenoxazine Chromophore on Optical, Electrochemical and Electrochromic Behaviors of Carbazole–Thiophene Derivatives." Polymers 16, no. 24 (2024): 3546. https://doi.org/10.3390/polym16243546.

Full text
Abstract:
Phenoxazine, as an organic-small-molecule chromophore, has attracted much attention for its potential electrochromic applications recently. To develop appealing materials, phenoxazine chromophores were introduced at the N-position of carbazole–thiophene pigment, yielding two novel monomers (DTCP and DDCP), whose chemical structures were characterized by NMR, HRMS and FTIR. The results of the optical property study indicate that little influence could be observed in the presence of the phenoxazine chromophore. Corresponding polymer films on the surface of an ITO/glass electrode were obtained th
APA, Harvard, Vancouver, ISO, and other styles
3

Iqbal, Nadeem, and Yoshio Ueno. "Synthesis of crowned phenoxazine derivatives." Monatshefte f�r Chemie Chemical Monthly 123, no. 6-7 (1992): 655–58. http://dx.doi.org/10.1007/bf00816860.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Kulszewicz-Bajer, Irena, Malgorzata Zagorska, Marzena Banasiewicz, et al. "Effect of the substituent position on the electrochemical, optical and structural properties of donor–acceptor type acridone derivatives." Physical Chemistry Chemical Physics 22, no. 16 (2020): 8522–34. http://dx.doi.org/10.1039/d0cp00521e.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Ferreira, João Carlos Canossa, Carla Lopes, Ana Preto, Maria Sameiro Torres Gonçalves, and Maria João Sousa. "Novel Nile Blue Analogue Stains Yeast Vacuolar Membrane, Endoplasmic Reticulum, and Lipid Droplets, Inducing Cell Death through Vacuole Membrane Permeabilization." Journal of Fungi 7, no. 11 (2021): 971. http://dx.doi.org/10.3390/jof7110971.

Full text
Abstract:
Phenoxazine derivatives such as Nile Blue analogues are assumed to be increasingly relevant in cell biology due to their fluorescence staining capabilities and antifungal and anticancer activities. However, the mechanisms underlying their effects remain poorly elucidated. Using S. cerevisiae as a eukaryotic model, we found that BaP1, a novel 5- and 9-N-substituted benzo[a]phenoxazine synthesized in our laboratory, when used in low concentrations, accumulates and stains the vacuolar membrane and the endoplasmic reticulum. In contrast, at higher concentrations, BaP1 stains lipid droplets and ind
APA, Harvard, Vancouver, ISO, and other styles
6

Ezeokonkwo, Mercy Amarachukwu, Kingsley Chizoba Iloka, Uchechukwu Chris Okoro, et al. "Synthesis and Antimicrobial Activity of New Derivatives of Angular Polycyclic Phenoxazine Ring System." Oriental Journal Of Chemistry 35, no. 4 (2019): 1320–26. http://dx.doi.org/10.13005/ojc/350410.

Full text
Abstract:
Synthesis of angular polycyclic phenoxazine derivatives incorporating different phenols is reported in 30-99% yields. O-arylation of 6-chlorodibenzo[a,j] phenoxazin-5-one with a variety of electron-deficient, electron-neutral and electron-rich phenols under the catalytic palladium (II) acetate/t-BuXphos system furnished the compounds of interest. The highest yields were obtained when the intermediate was coupled with electron-rich phenols. IR, 1H-NMR, 13C-NMR and Mass spectra data, confirmed the structures of all the synthesized compounds. Study on the in vitro biological evaluation of the com
APA, Harvard, Vancouver, ISO, and other styles
7

Zhang, Lu, Xin Huang, Shan Zhen, et al. "Pd-Catalyzed double N-arylation of primary amines to synthesize phenoxazines and phenothiazines." Organic & Biomolecular Chemistry 15, no. 30 (2017): 6306–9. http://dx.doi.org/10.1039/c7ob01540b.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Sridhar, M. A., M. Ramegowda, N. K. Lokanath, J. Shashidhara Prasad, G. B. Ere Gowda, and K. N. Thimmaiah. "Structural Studies of Some Phenoxazine Derivatives." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 326, no. 1 (1999): 189–214. http://dx.doi.org/10.1080/10587259908025415.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Pal, Sanjima, V. Badireenath Konkimalla, Laxmi Kathawate та ін. "Targeting a chemorefractory COLO205 (BRAF V600E) cell line using substituted benzo[α]phenoxazines". RSC Advances 5, № 100 (2015): 82549–63. http://dx.doi.org/10.1039/c5ra14949e.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Ibraheem, Israa, and Suad Al.Araji. "Synthesis of New N-Substituted Phenoxazine Derivatives." Baghdad Science Journal 13, no. 2 (2016): 360–65. http://dx.doi.org/10.21123/bsj.2016.13.2.2ncc.0360.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Phenoxazine derivatives"

1

Ramegowda, M. "Structural investigations of some phenoxazine derivatives." Thesis, 1997. http://hdl.handle.net/2009/1649.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Soriano, Juarez Eduardo Salvador. "Synthesis and Characterization of New Near-Infrared Chromophores: Cyanine and Phenoxazine Derivatives." 2015. http://scholarworks.gsu.edu/chemistry_theses/76.

Full text
Abstract:
This thesis reports the synthesis of new near infrared dyes in three chapters. The first two chapters outline the synthetic procedure for synthesizing mono- and pentamethine cyanine dyes. The initial chapter encompasses the synthesis of asymmetric monomethine dyes with red-shifted optical properties. The second chapter involves the synthesis and assessment of new symmetrical quinolin-4-yl and phenanthridin-6-yl pentamethine dyes as potential oxidative DNA cleavage agents. The last chapter of the thesis details the synthesis and evaluation of new phenoxizinum dyes as contrast agents for insulun
APA, Harvard, Vancouver, ISO, and other styles
3

Ferreira, João Carlos Canossa. "Characterization of vacuole permeabilization and HMGB1 nuclear release in the yeast cell death induced by a benzo[a]phenoxazine derivative." Master's thesis, 2017. http://hdl.handle.net/1822/45755.

Full text
Abstract:
Dissertação de mestrado em Genética Molecular<br>The number of antifungal agents approved for use in humans is still very limited and resistance to the existing ones is often found, thus revealing the need for the development of new antifungal drugs. Phenoxazine derivatives have assumed an increasing importance in life sciences since they present antiproliferative proprieties which potentiate their utilization as antitumor and antimicrobial agents. We have recently found that one new phenoxazine derivative (MSG-111-cd3), induces cell death in Saccharomyces cerevisiae and accumulates at th
APA, Harvard, Vancouver, ISO, and other styles

Books on the topic "Phenoxazine derivatives"

1

Веселков, Алексей Никонович, and Alexei N. Veselkov. Anti-cancer drug design: Biol. a. biophys. aspects of synthetic phenoxazone derivatives. SEVNTU press, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Phenoxazine derivatives"

1

Kitson, Trevor M., Kathryn E. Kitson, and Gordon J. King. "Covalent Modification of Sheep Liver Cytosolic Aldehyde Dehydrogenase by the Oxidative Addition of Coloured Phenoxazine, Phenothiazine and Phenazine Derivatives." In Advances in Experimental Medicine and Biology. Springer US, 1999. http://dx.doi.org/10.1007/978-1-4615-4735-8_11.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Yoshida, S., K. Kozawa, and T. Uchida. "Electrical properties of sublimed films of phenothiazine and phenoxazine derivatives." In Advanced Materials '93. Elsevier, 1994. http://dx.doi.org/10.1016/b978-1-4832-8380-7.50156-5.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Phenoxazine derivatives"

1

Sokolskaya, S. Y., B. P. Myasnikov, E. A. Guseva, P. N. Kamzeeva, P. V. Sergiev, and A. V. Aralov. "MODIFIED (2’-DEOXY)ADENOSINES AND PHENOXAZINE AS AUTOPHAGY INDUCERS." In XI МЕЖДУНАРОДНАЯ КОНФЕРЕНЦИЯ МОЛОДЫХ УЧЕНЫХ: БИОИНФОРМАТИКОВ, БИОТЕХНОЛОГОВ, БИОФИЗИКОВ, ВИРУСОЛОГОВ, МОЛЕКУЛЯРНЫХ БИОЛОГОВ И СПЕЦИАЛИСТОВ ФУНДАМЕНТАЛЬНОЙ МЕДИЦИНЫ. IPC NSU, 2024. https://doi.org/10.25205/978-5-4437-1691-6-274.

Full text
Abstract:
Autophagy inducers are regarded as a promising class of molecules with potential for use in the treatment of cancer and neurodegenerative diseases. A total of six novel autophagy activators have been identified, belonging to two distinct chemical classes: 2’-deoxyadenosine derivatives and phenoxazine analogues. These compounds activate autophagy by the AMPK-dependent pathway, and exhibit greater activity than the known autophagy modulator AICAr.
APA, Harvard, Vancouver, ISO, and other styles
2

Agabekov, Vladimir E., and Olga E. Ignasheva. "Optical and masking properties of vacuum photoresists based on benzo[a]phenoxazine derivatives." In Optical Information Science and Technology, edited by Andrei L. Mikaelian. SPIE, 1998. http://dx.doi.org/10.1117/12.301422.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Agabekov, Vladimir E., Olga E. Ignasheva, and Vladimir N. Belyatsky. "Vacuum-vapor-deposited films based on benzo(a)phenoxazine derivatives under surface plasma fluorination." In Microlithography '97, edited by Regine G. Tarascon-Auriol. SPIE, 1997. http://dx.doi.org/10.1117/12.275875.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Stüber, W., D. Schiwek, U. Becker, and N. Heimburger. "NEW CHROMOGENIC SUBSTRATES FOR THE DETERMINATION OF COAGULATION AND FIBRINOLYSIS ENZYMES." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644323.

Full text
Abstract:
A new type of chromogenic substraces based on derivatives of phenoxazine is presented. Particularly interesting is the blue dye 7-amino-3-diethylamino-8-methylphenoxazine (ADMP) with a molar extinktion coefficient of about 80,000 at 624 nm. Peptides were linked to the aminogroup of the dye and red coloured substrates were obtained with a λmax value of about 540 nm. On account of the distinct difference of the λmax values and the negligable influence of the absorption peaks of the acylated and the free dye this chromophore is suitable for the synchesis of substrates. Besides the spectral proper
APA, Harvard, Vancouver, ISO, and other styles
5

Ferreira, João Carlos, Maria Sameiro Gonçalves, Ana Preto, and Maria Sousa. "The potential of novel benzo[&lt;em&gt;a&lt;/em&gt;]phenoxazine derivatives for colorectal cancer treatment." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11522.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Agabekov, Vladimir E., Yurii I. Gudimenko, and Olga E. Ignasheva. "Vacuum-vapor-deposited thin films of benzo[a]phenoxazone-5 derivatives as photoresist layers: properties versus deposition parameters." In International Conference on Microelectronics, edited by Andrzej Sowinski, Jan Grzybowski, Witold T. Kucharski, and Ryszard S. Romaniuk. SPIE, 1992. http://dx.doi.org/10.1117/12.131006.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Gonçalves, M. Sameiro, Maria Inês Leitão, B. Rama Raju, and Maria João Sousa. "Antiproliferative Activity of 2,3,6,7-Tetrahydro-1H-Benzo[a]Quinolizino[1,9-hi]Phenoxazin-14(5H)-Iminium Chloride Derivatives." In The 18th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b027.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Phenoxazine derivatives' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography