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Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives

Year 2018, , 105 - 115, 28.12.2018
https://doi.org/10.32571/ijct.446539

Abstract

A new series of 5-Chloroisatin derivatives were
synthesied and characterises with different characterization methods such as 1H-NMR
and13C-NMR spectroscopy, and then tested for their myorelaxant
activity.
Computational investigations of the
compounds 1a-3a, 2b and 4b on the muscle-relaxing effects
performance
were performed
by using the DFT method with B3LYP functional
. The
result of descriptors calculation revealed that the theoretical approach
was in
good agreement
with the reported experimental data.

References

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  • 2. Pandeya, S. N.; Sriram, D.; Nath, G.; De Clercq, E. Pharm. Acta Helv 1999, 74 (11).
  • 3. Sarangapani, M.; Reddy, V. M.. Indian J. Pharm. Sci. 1996, 58 (4), 147.
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  • 15. Frisch, M.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, Ga. Inc., Wallingford, CT, 2009, 200.
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  • 25. Kikuchi, O. Mol. Inform. 1987, 6 (4), 179–184.
  • 26. Khaled, K. F. Appl. Surf. Sci. 2010, 256 (22), 6753–6763.
  • 27. Tribak, Z.; Rodi, Y. K.; Haoudi, A.; Skalli, M. K.; Mazzah, A.; Ouzidan, Y.; Senhaji, O.; Essassi, E. M.; J. Mar. Chim. Heterocycl. 2017, 16, 110–118.
  • 28. Tribak, Z.; R. Ghibate.; Skalli, M. K.; Senhaji, O.;Rodi, Y. K. Inter. J. Sci. Tech. Eng. 2016, 3 (06), 257–262.
  • 29. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Chem. 2017, 5 (2), 91–95.
  • 30. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Chem. 2017, 4 (5), 2–7.
  • 31. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Sci. Res. 2017, 6 (7), 1069–1074.
  • 32. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H. IUCrData 2016, 1 (6), x160913.
  • 33. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H.. IUCrData 2016, 1 (6), x160854.
  • 34. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H. IUCrData 2016, 1 (6), x160862.
  • 35. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H.. IUCrData 2016, 1 (6), x160971.
  • 36. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Eng. Manag. Sci. 2017. 3(8) 837-841
  • 37. Tribak, Z.; Amin, O. El; Skalli, M. K.; Senhaji, O.; Rodi, Y. K.; Iraqui, M. H. Int. J. Eng. Res. Appl. 2017, 7 (6), 21–24.
  • 38. Tribak, Z.; Amin, O. El; Skalli, M. K.; Senhaji, O.; Rodi, Y. K.; Iraqui, M. H. Int. J. Eng. Res. Appl. 2017, 7 (6), 66–70.
Year 2018, , 105 - 115, 28.12.2018
https://doi.org/10.32571/ijct.446539

Abstract

References

  • 1. Tribak, Z.; Skalli, M. K.; Haoudi, A.; Rodi, Y. K.; Senhaji, O.; Essassi, E. M. IMedPub Journals. 2018, 3, 1–4.
  • 2. Pandeya, S. N.; Sriram, D.; Nath, G.; De Clercq, E. Pharm. Acta Helv 1999, 74 (11).
  • 3. Sarangapani, M.; Reddy, V. M.. Indian J. Pharm. Sci. 1996, 58 (4), 147.
  • 4. Popp, F. D.; Parson, R.; Donigan, B. E. J. Heterocycl. Chem. 1980, 17 (6), 1329–1330.
  • 5. Pandeya, S. N.; Smitha, S.; Jyoti, M.; Sridhar, S. K. Acta Pharm 2005, 55 (1), 27–46.
  • 6. Singh, G. S.; Singh, T.; Lakhan, R. ChemInform 1998, 29 (17).
  • 7. Bhattacharya, S. K.; Chakrabarti, A. Indian J. Exp. Biol. 1998, 36 (1), 118–121.
  • 8. Tribak, Z.; Kharbach, Y.; Haoudi, A.; Skalli, M. K.; Rodi, Y. K.; El Azzouzi, M.; Aouniti, A.; Hammouti, B.; Senhaji, O. J. Mater. Environ. Sci. 2016, 7 (6), 2006–2020.
  • 9. Tribak, Z.; Kandri Rodi, Y.; Elmsellem, H.; Abdel-Rahman, I.; Haoudi, A.; Skalli, M. K.; Kadmi, Y.; Hammouti, B.; Ali Shariati, M.; Essassi, E. M. J. Mater. Environ. Sci 2017, 8 (3), 1116–1127.
  • 10. Tribak, Z.; Haoudi, A.; Skalli, M. K.; Rodi, K. Y.; El Azzouzi, M.; Aouniti, A.; Hammouti, B.; Senhaji, O. J. Mater. Environ. Sci. 2017, 8 (1), 299–309.
  • 11. Obot, I. B.; Obi-Egbedi, N. O.; Umoren, S. A. Int. J. Electrochem. Sci 2009, 4 (6), 863–877.
  • 12. Zhang, S. G.; Lei, W.; Xia, M. Z.; Wang, F. Y. J. Mol. Struct. THEOCHEM 2005, 732 (1–3), 173–182.
  • 13. Irfan, A.; Al-Sehemi, A. G.; Asiri, A. M.; Nadeem, M.; Alamry, K. A. Comput. Theor. Chem. 2011, 977 (1–3), 9–12.
  • 14. Irfan, A.; Hina, N.; Al-Sehemi, A. G.; Asiri, A. M. J. Mol. Model. 2012, 18 (9), 4199–4207.
  • 15. Frisch, M.; Trucks, G. W.; Schlegel, H. B.; Scuseria, G. E.; Robb, M. A.; Cheeseman, J. R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, Ga. Inc., Wallingford, CT, 2009, 200.
  • 16. Chattaraj, P. K.; Roy, D. R. Chem. Rev. 2007, 107 (9), PR46-PR74.
  • 17. Wang, H.; Wang, X.; Wang, H.; Wang, L.; Liu, A. J. Mol. Model. 2007, 13 (1), 147–153.
  • 18. Siaka, A. A.; Edd, N. O.; Idris, S. O.; Magaji, L. Res. J. Appl. Sci. 2011, 6 (7–12), 487–493.
  • 19. Eddy, N. O.; Stoyanov, S. R.; Ebenso, E. E. Int. J. Electrochem. Sci 2010, 5, 1127–1150.
  • 20. Tribak, Z.; Haoudi, A.; Rodi, Y. K.; Elmsellem, H.; Skalli, M. K. Mor. J. Chem. 2016, 4, 1157–1163.
  • 21. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K.; Haoudi, A.; Essassi, E. M. Am. Inter. J. Res. Formal. Appl. Nat. Sci. 2017.1, 41–50.
  • 22. Chda, A.; El Kabbaoui, M.; Chokri, A.; El Abida, K.; Tazi, A.; Cheikh, R. Ben. Eur. J. Med. Plants 2016, 11 (2), 1–13.
  • 23. Obi-Egbedi, N. O.; Obot, I. B.; El-Khaiary, M. I.; Umoren, S. A.; Ebenso, E. E.. Int. J. Electrochem. Sci 2011, 6, 5649–5675.
  • 24. Özcan, M.; Solmaz, R.; Kardaş, G.; Dehri, I. Colloids Surfaces A Physicochem. Eng. Asp. 2008, 325 (1–2), 57–63.
  • 25. Kikuchi, O. Mol. Inform. 1987, 6 (4), 179–184.
  • 26. Khaled, K. F. Appl. Surf. Sci. 2010, 256 (22), 6753–6763.
  • 27. Tribak, Z.; Rodi, Y. K.; Haoudi, A.; Skalli, M. K.; Mazzah, A.; Ouzidan, Y.; Senhaji, O.; Essassi, E. M.; J. Mar. Chim. Heterocycl. 2017, 16, 110–118.
  • 28. Tribak, Z.; R. Ghibate.; Skalli, M. K.; Senhaji, O.;Rodi, Y. K. Inter. J. Sci. Tech. Eng. 2016, 3 (06), 257–262.
  • 29. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Chem. 2017, 5 (2), 91–95.
  • 30. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Chem. 2017, 4 (5), 2–7.
  • 31. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Sci. Res. 2017, 6 (7), 1069–1074.
  • 32. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H. IUCrData 2016, 1 (6), x160913.
  • 33. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H.. IUCrData 2016, 1 (6), x160854.
  • 34. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H. IUCrData 2016, 1 (6), x160862.
  • 35. Tribak, Z.; Kandri Rodi, Y.; Haoudi, A.; Essassi, E. M.; Capet, F.; Zouihri, H.. IUCrData 2016, 1 (6), x160971.
  • 36. Tribak, Z.; Skalli, M. K.; Senhaji, O.; Rodi, Y. K. Inter. J. Adv. Eng. Manag. Sci. 2017. 3(8) 837-841
  • 37. Tribak, Z.; Amin, O. El; Skalli, M. K.; Senhaji, O.; Rodi, Y. K.; Iraqui, M. H. Int. J. Eng. Res. Appl. 2017, 7 (6), 21–24.
  • 38. Tribak, Z.; Amin, O. El; Skalli, M. K.; Senhaji, O.; Rodi, Y. K.; Iraqui, M. H. Int. J. Eng. Res. Appl. 2017, 7 (6), 66–70.
There are 38 citations in total.

Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Articles
Authors

Zineb Tribak 0000-0002-2169-9856

Alae Chda This is me

Mohammed Khalid Skalli This is me

Amal Haoudi This is me

Youssef Kandri Rodi This is me

Omar Senhaji This is me

El Mokhtar Essassi This is me

Rachid Ben Cheikh This is me

Kaouakib El Abida This is me

Publication Date December 28, 2018
Published in Issue Year 2018

Cite

APA Tribak, Z., Chda, A., Skalli, M. K., Haoudi, A., et al. (2018). Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives. International Journal of Chemistry and Technology, 2(2), 105-115. https://doi.org/10.32571/ijct.446539
AMA Tribak Z, Chda A, Skalli MK, Haoudi A, Rodi YK, Senhaji O, Essassi EM, Cheikh RB, El Abida K. Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives. Int. J. Chem. Technol. December 2018;2(2):105-115. doi:10.32571/ijct.446539
Chicago Tribak, Zineb, Alae Chda, Mohammed Khalid Skalli, Amal Haoudi, Youssef Kandri Rodi, Omar Senhaji, El Mokhtar Essassi, Rachid Ben Cheikh, and Kaouakib El Abida. “Theoretical Approach Using DFT and Muscle Relaxant Effects of 5-Chloroisatin Derivatives”. International Journal of Chemistry and Technology 2, no. 2 (December 2018): 105-15. https://doi.org/10.32571/ijct.446539.
EndNote Tribak Z, Chda A, Skalli MK, Haoudi A, Rodi YK, Senhaji O, Essassi EM, Cheikh RB, El Abida K (December 1, 2018) Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives. International Journal of Chemistry and Technology 2 2 105–115.
IEEE Z. Tribak, “Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives”, Int. J. Chem. Technol., vol. 2, no. 2, pp. 105–115, 2018, doi: 10.32571/ijct.446539.
ISNAD Tribak, Zineb et al. “Theoretical Approach Using DFT and Muscle Relaxant Effects of 5-Chloroisatin Derivatives”. International Journal of Chemistry and Technology 2/2 (December 2018), 105-115. https://doi.org/10.32571/ijct.446539.
JAMA Tribak Z, Chda A, Skalli MK, Haoudi A, Rodi YK, Senhaji O, Essassi EM, Cheikh RB, El Abida K. Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives. Int. J. Chem. Technol. 2018;2:105–115.
MLA Tribak, Zineb et al. “Theoretical Approach Using DFT and Muscle Relaxant Effects of 5-Chloroisatin Derivatives”. International Journal of Chemistry and Technology, vol. 2, no. 2, 2018, pp. 105-1, doi:10.32571/ijct.446539.
Vancouver Tribak Z, Chda A, Skalli MK, Haoudi A, Rodi YK, Senhaji O, Essassi EM, Cheikh RB, El Abida K. Theoretical approach using DFT and muscle relaxant effects of 5-Chloroisatin Derivatives. Int. J. Chem. Technol. 2018;2(2):105-1.