153
Views
2
CrossRef citations to date
0
Altmetric
Research Articles

Synthesis of Some Novel Indoline-2,3-Dione Derivatives and the Influence of Gamma Irradiation on Their Biological Activities

, , &
Pages 6846-6860 | Received 23 Aug 2021, Accepted 29 Sep 2021, Published online: 23 Oct 2021

References

  • Humayun Pervez, Zahid Hussain Chohan, Muhammad Ramzan, Faiz-Ul-Hassan Nasim, and Khalid Mohammed Khan, “Synthesis and Biological Evaluation of Some New N(4)-Substituted Isatin-3-Thiosemicarbazones,” Journal of Enzyme Inhibition and Medicinal Chemistry 24, no. 2 (2009): 437–46.
  • H. Pervez, M. S. Iqbal, M. Y. Tahir, F. U. H. Nasim, M. I. Choudhary, and K. M. Khan, “In Vitro Cytotoxic, Antibacterial, Antifungal and Urease Inhibitory Activities of Some N4- Substituted Isatin-3-Thiosemicarbazones,”Journal of Enzyme Inhibition and Medicinal Chemistry 23, no. 6 (2008): 848–54.
  • S. Y. Abbas, A. A. Farag, Y. A. Ammar, A. A. Atrees, A. F. Mohamed, and A. A. El-Henawy, “Synthesis, Characterization, and Antiviral Activity of Novel Fluorinated Isatin Erivatives,” Monatshefte Für Chemie - Chemical Monthly 144, no. 11 (2013): 1725–33.
  • M. Verma, S. N. Pandeya, K. N. Singh, and J. P. Stables, “Anticonvulsant Activity of Schiff Bases of Isatin Derivatives,” Acta Pharmaceutica (Zagreb, Croatia) 54, no. 1 (2004): 49–56.
  • M. A. Ganim, M. C. Baloglu, A. Aygun, Y. C. Altunoglu, H. S. Sayiner, F. Kandemirli, and F. Sen, “Analysis of DNA Protection, Interaction and Antimicrobial Activity of Isatin Derivatives,” International Journal of Biological Macromolecules 122 (2019): 1271–8.
  • D. R. Brki, A. R. Bozi, A. D. Marinkovi, M. K. Milci, N. Z. Prlainovi, F. H. Assaleh, I. N. Cvijeti, J. B. Nikoli, and S. Z. Drmani, “Detailed Solvent, Structural, Quantum Chemical Study and Antimicrobial Activity of Isatin Schiff Base,” Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 196 (2018): 16–30.
  • S. Madhira, K. Mandava, S. Manda, R. Sai Prasanna, and T. Vijayalaxmi, “Synthesis and Evaluation of Some Novel N, NDialkylaminoalkoxy-2-Oxo-Indole-3-Ylidene Benzohydrazides as Anticonvulsant Agents,” IOSR Journal of Pharmacy and Biological Sciences 12, no. 02 (2017): 84–93.
  • S. Saranya, J. Haribabu, V. Namboothiri, V. Palakkeezhillam, P. Jerome, K. Gomathi, K. K. Rao, R. Karvembu, and D. Gayathri, “Molecular Structures, Hirshfeld Analysis and Biological Investigations of Isatin Based Thiosemicarbazones,” Journal of Molecular Structure 1198 (2019): 126904.
  • D. Havrylyuk, N. Kovach, B. Zimenkovsky, O. Vasylenko, and R. Lesyk, “Synthesis and Anticancer Activity of Isatin-Based Pyrazolines and Thiazolidines Conjugates,” Archiv der Pharmazie 344, no. 8 (2011): 514–22.
  • O. A. Abdou and A. M. A. Mamdouh, "Synthesis of Some New Thiazoles and Pyrazolo[1,5-a]pyrimidines Containing an Antipyrine Moiety," Synthetic Communication., 40 (2010): 1539–1550.
  • A. O. Abdelhamid, V. B. Baghos, and M. M. A. Halim, “Synthesis of Heterocyclic Containing Benzoxazole Moiety,” Phosphorus, Sulphur, and Silicon 183, no. 6 (2008): 1313–22.
  • N. M. Rateb and O. Abdou, “Synthesis of 2,3-Dihydro-1,3,4-Thiadiazole, Thiazole, and Triazolo[4,3-a]Pyrimidine Derivatives from Ethyl Benzoylacetate,” Heteroatom Chemistry 15, no. 2 (2004): 107–13.
  • A. D. Russell, “Bacterial Spores and Chemical Sporicidal Agents,” Clinical Microbiology Reviews 3, no. 2 (1990): 99–119.
  • R. V. Chambhare, B. G. Khadse, A. S. Bobde, and R. H. Bhekar, “Synthesis and Preliminary Evaluation of Some N-[5-(2-Furanyl)-2-Methyl-4-Oxo-4H-Thieno[2,3-d]Pyrimidin-3-yl]-Carboxamide and 3-Substituted-5-(2-Furanyl)-2-Methyl-3H-Thieno[2,3-d]Pyrimidin-4-Ones as Antimicrobial Agents,” European Journal of Medicinal Chemistry 38, no. 1 (2003): 89–100.
  • M. Wahab Khan, M. Jahangir Alam, M. A. Rashid, and R. Chowdhury, “A New Structural Alternative in Benzo[b]Furans for Antimicrobial Activity,” Bioorganic & Medicinal Chemistry 13, no. 16 (2005): 4796–805.
  • C. Praveen, A. Ayyanar, and P. T. Perumal, “Practical Synthesis, Anticonvulsant, and Antimicrobial Activity of N-Allyl and N-Propargyl di(Indolyl)Indolin-2-Ones,” Bioorganic & Medicinal Chemistry Letters 21, no. 13 (2011): 4072–7.
  • S. N. Pandeya, D. Sriram, G. Nath, and E. Declercq, “Synthesis, Antibacterial, Antifungal and anti-HIV Activities of Schiff and Mannich Bases Derived from Isatin Derivatives and N-[4-(4'-Chlorophenyl)Thiazol-2-yl] Thiosemicarbazide,” European Journal of Pharmaceutical Sciences 9, no. 1 (1999): 25–31.
  • F. A. Khan and A. Maalik, “Advances in Pharmacology of Isatin and Its Derivatives,” Tropical Journal of Pharmaceutical Research 14, no. 10 (2015): 1937–42.
  • A. Amal Raj, R. Raghunathan, M. R. Sridevikumari, and N. Raman, “Synthesis, Antimicrobial and Antifungal Activity of a New Class of Spiro Pyrrolidines,” Bioorganic & Medicinal Chemistry. no. 11 (2003): 407–19.
  • S. V. Tiwari, N. S. Sharif, R. I. Gajare, J. A. S. Vazque, J. N. Sangshetti, M. D. Damale, GAnna. Pratima, and A. P. G. Nikalje, “New 2-Oxoindolin Phosphonates as Novel Agents to Treat Cancer: A Green Synthesis and Molecular Modeling,” Molecules 23, no. 8 (2018): 1981.
  • E. Mansour, A. Aboelnaga, E. M. Nassar, and S. I. Elewa, “A New Series of Thiazolyl Pyrazoline Derivatives Linked to Benzo[1,3]Dioxole Moiety: Synthesis and Evaluation of Antimicrobial and Anti-Proliferative Activities,” Synthetic Communications 50, no. 3 (2020): 368–79.
  • Z. E. El-Bazza, S. Y. El-Tablawy, A. S. E. Mohamed, and H. A. Nasser, “Selection of Gamma Irradiation Dose from Sterilizing Eye Makeup Preparations,” Egyptian Journal of Microbiology 45 (2010): 131–46. ‏
  • D. Todorović, I. Petrović, M. Todorović, G. Cuttone, and A. Ristić-Fira, “Early Effects of Gamma Rays and Protons on Human Melanoma Cell Viability and Morphology,” Journal of Microscopy 232, no. 3 (2008): 517–21.‏
  • Debabrota Ghosal, Marina V. Omelchenko, Elena K. Gaidamakova, Vera Y. Matrosova, Alexander Vasilenko, Amudhan Venkateswaran, Min Zhai, Heather M. Kostandarithes, Hassan Brim, Kira S. Makarova, et al. “How Radiation Kills Cells: Survival of Deinococcus Radiodurans and Shewanella Oneidensis under Oxidative Stress,” FEMS Microbiology Reviews 29, no. 2 (2005): 361–75. ‏
  • Sandra P. Santos, Edward P. Mitchell, Henri G. Franquelim, Miguel A. R. B. Castanho, Isabel A. Abreu, and Célia V. Romão, “Dps from Deinococcus Radiodurans: Oligomeric Forms of Dps1 with Distinct Cellular Functions and Dps2 Involved in Metal Storage,” The FEBS Journal 282, no. 22 (2015): 4307–27. ‏
  • B. Boyan, J. Hooper, and J. Parisot, “Principles of Assessing Bacterial Susceptibility to Antibiotics Using the Agar Diffusion Method,” The Journal of Antimicrobial Chemotherapy 61, no. 6 (2008): 1295–301.
  • E. A. Christensen, and H. Kristensen, “Radiation-Resistance of Microorganisms from Air in Clean Premises,” APMIS 89 (1981): 293–301.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.