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- In vitro anti-trypanosomal activity of 3-(aryl)-6-piperazin1,2,4-triazolo[3,4-a]phthalazines-loaded ultrathin polymeric particles: effect of polymer type and particle size. Karina González, Ender Medina, Elena Aguilera, Gema González, Marcos A. Sabino, Angel H. Romero
, RSC Pharm.
, 2024
, 1
, 108
- Centroid⋯centroid and hydrogen bond interactions as robust supramolecular units for crystal engineering: X-ray crystallographic, computational and urease inhibitory investigations of 1,2,4-triazolo[3,4-a]phthalazines. Sumera Zaib, Aliya Ibrar, Marriyam Ramay, Shabab Zahra, Tuncer Hökelek, Jim Simpson, Christopher John McAdam, Nasser S. Awwad, Hala A. Ibrahium, Antonio Frontera, Imtiaz Khan
, CrystEngComm
, 2022
, 24
, 5324
- Synthesis and biological evaluation of 1,2,4-triazoloazines as potent anticancer agents. Polina O. Serebrennikova, Julia A. Paznikova, Eva A. Kirnos, Irina A. Utepova, Elizaveta D. Kazakova, Vladimir F. Lazarev, Liubov S. Kuznetcova, Boris A. Margulis, Irina V. Guzhova, Oleg N. Chupakhin, Alexey P. Sarapultsev
, New J. Chem.
, 2023
, 47
, 18325
- Optimization of phthalazin-based aryl/heteroarylhydrazones to design new promising antileishmanicidal agents: synthesis and biological evaluation of 3-aryl-6-piperazin-1,2,4-triazolo[3,4-a]phthalazines. Angel H. Romero, Noris Rodríguez, Oscar G. Ramírez
, New J. Chem.
, 2020
, 44
, 13807
- Solid-state studies of phthalazinylhydrazones and triazolophthalazines: the role of the nitro group. Agata Trzesowska-Kruszynska
, CrystEngComm
, 2015
, 17
, 7702
- Small hybrid heteroaromatics: resourceful biological tools in cancer research. Vikrant Abbot, Poonam Sharma, Saurabh Dhiman, Malleshappa N. Noolvi, Harun M. Patel, Varun Bhardwaj
, RSC Adv.
, 2017
, 7
, 28313
- Triazines and related products. Part XVI. Synthesis of triazolotriazines by cyclisation of 3-hydrazino-1,2,4-triazines and 3-hydrazino-1,2,4-triazoles. Elizabeth Jane Gray, Malcolm F. G. Stevens
, J. Chem. Soc., Perkin Trans. 1
, 1976
, 1492
- Synthesis and structure of some azolo[a]pyrimidines, 2,6,7,8-tetrahydro-1H-cyclopenta[e]azolo[a]pyrimidines, 6,7-dihydro-5H-cyclopenta[f]azolo[a]pyrimidines, 7,8-dihydro-6H-cyclopenta[f]-s-triazolo[4,3-b]pyridazine, 5,6,7,8-tetrahydro-azolo[b]quinazolines, 6,7,8,9-tetrahydroazolo[a]quinazolines, and 7,8,9,10-tetrahydro-s-triazolo[3,4-a]phthalazine. Joginder S. Bajwa, Peter J. Sykes
, J. Chem. Soc., Perkin Trans. 1
, 1979
, 3085
- N–N bond fission and ring opening in s-triazolo[3,4-a]phthalazines. K. T. Potts, C. A. Lovelette
, Chem. Commun. (London)
, 1968
, 845
- Development of a facile and sensitive fluorimetric derivatization reagent for detecting formaldehyde. Chao Liu, An-Wei Cheng, Xue-Kui Xia, Yu-Fa Liu, Sheng-Wen He, Xu Guo, Jin-Yue Sun
, Anal. Methods
, 2016
, 8
, 2764