Dergiler / Turkish Journal of Chemistry / 2004 / Cilt: 28 - Sayı: 4

Synthesis and antinociceptive activity of 2-[(2-oxobenzothiazolin_3-yl)methlyl]-5-aminoalkyl/aryl-1,3,4,-thiadiazole

Sayfa
461–468
Yayın Tarihi
2022-11-05
DOI
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Among these compounds, 2-[(2-oxobenzothiazolin-3-yl)methyl]-5-aminomethyl-1,3,4-thiadiazole (5a) was found to be significantly more active than the others and the standards in all the tests.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Ten 2-[(2-oxobenzothiazolin-3-yl)methyl]-5-aminoalkyl/aryl-1,3,4-thiadiazole derivatives were synthesized.
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Temel Bulgular & Veri:The chemical structures of these compounds were elucidated by their FT-IR and $^1H-NMR$ spectral data, as well as their elemental analyses.
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Sonuç & Katkı:Among these compounds, 2-[(2-oxobenzothiazolin-3-yl)methyl]-5-aminomethyl-1,3,4-thiadiazole (5a) was found to be significantly more active than the others and the standards in all the tests.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Ten 2-[(2-oxobenzothiazolin-3-yl)methyl]-5-aminoalkyl/aryl-1,3,4-thiadiazole derivatives were synthesized. The chemical structures of these compounds were elucidated by their FT-IR and $^1H-NMR$ spectral data, as well as their elemental analyses. The compounds were tested for antinociceptive activity. Among these compounds, 2-[(2-oxobenzothiazolin-3-yl)methyl]-5-aminomethyl-1,3,4-thiadiazole (5a) was found to be significantly more active than the others and the standards in all the tests.

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Bu Makaleye Atıf Yap

ÖNKOL, T., ŞAHİN, M. F., ÇAKIR, B., EROL, K., YILDIRIM, E. (2022). Synthesis and antinociceptive activity of 2-[(2-oxobenzothiazolin_3-yl)methlyl]-5-aminoalkyl/aryl-1,3,4,-thiadiazole. Turkish Journal of Chemistry, Cilt: 28 - Sayı: 4, 461–468. https://ajindex.com/articles/602242

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Kaynakça (22)

  1. R. Şimşek, Y. Altaş, C. Şafak, U. Abbasoglu and B. Ozcelik, Farmaco, 50, 893-894 (1995)
  2. K. Tsurumi, V. Hiramatsu, M. Nozaki, F.J. Hayashi and H. Fujimura, Arzneim.-Forch/Drug Res., 22, 724-731 (1972)
  3. J. Vanderberk, L.E.J. Kennis, M.J.M.C. Van der A and A.H.M.T. Albert US 672919 (1976) [Chem. Abst.,88, 50920n, (1978)] 4.H. Uçar, S. Cacciaguerra, S. Spampinato, K.V. Derpoorten, M. Isa, M. Kanyonyo and J.H. Poupaert, Eur. J.Pharm., 335, 267-273 (1997)
  4. H. Uçar, K. Derpoorten, S. Cacciaguerra, S. Spampinato, J.P. Stables, P. Depovere, M. Isa, B. Masereel, J.Delarge and J. P. Poupaert, J. Med. Chem., 41, 1138-1143 (1998)
  5. B. Çakır, S.D. Dogruer, S. Unlu and M.F. Sahin, J. Fac. Pharm. Gazi, 14, 25-30 (1997)
  6. B. Çakır, S.D. Dogruer, E. Yeşilada and M.F. Şahin, J. Fac. Pharm. Gazi, 14, 92-98 (1997)
  7. B. Çakır, S.D. Dogruer, S. Ünlü, E. Yeşilada and M.F. Şahin, J. Fac. Pharm. Gazi, 14, 103-109 (1997)
  8. S. Rollas, S. Karakuş, B.B. Durgun, M. Kiraz and H. Erdeniz, Farmaco, 51 (12), 811-814 (1996)
  9. A. Varvaresou, A. Tsantili-Kakoulidou, T. Siatra-Papastaikoudi and E. Tiligada, Arzneim.-Forsch./Drug Res., 50, 48-54 (2000)
  10. N. Terzioğlu, N. Karalı, A. Gürsoy, G.Ötük, M. Kiraz and Z. Erturan, Acta Pharmaceutica Turcica, 40,77-82 (1998)
  11. H. Chen, Z. Li and Y. Han, J. Agric. Food Chem., 48, 5312-5315 (2000)
  12. Y. Nomoto, H. Takaı, T. Hırata, M. Teranıshı, T. Ohno and K. Kubo, Chem. Pharm. Bull., 39, 86-90 (1991)
  13. A. Foroumadi, M. Mirzaei and A. Shafiee, Pharmazie, 56, 610-612 (2001)
  14. M.G. Mamolo, V. Falagiani, D. Zampieri, L. Vio and E. Banfi, Farmaco, 56, 587-592 (2001)
  15. F. Clerici, D. Pocar, M. Guido, A. Loche, V. Perlini and M. Brufani, J. Med. Chem., 44, 931-936 (2001)
  16. A. Varvaresou, T. Siatra-Papastaikoudi, A. Tsotinis, A. Tsantili-Kakoulidou and A. Vamvakides, Farmaco,53, 320-326 (1998)
  17. S. Schenone, O. Bruno, A. Ranise, F. Bondavalli, W. Filippelli, G. Falcone, B. Piucci and S. Sorrentino,Farmaco; 53, 586-589 (1998)
  18. S. Schenone, O. Bruno, A. Ranise, F. Bondavalli, W. Filippelli, G. Falcone, L. Giordano and M.R. Vitelli,Bioorg. Med. Chem., 9, 2149-2153 (2001)
  19. A.A. Fargnaly, A.A. Bekhit and J.Y. Park, Arch. Pharm. Pharm. Med. Chem., 333, 53-57 (2000)
  20. E. Palaska, G. Sahin, P. Kelicen, N.T. Durlu and G. Altınok, Farmaco, 57, 101-107 (2002)
  21. T.H. Fife, J.E.C. Hutchins and M.S. Wang, J. Am. Chem. Soc., 97, 5878-5882 (1975)
  22. J.J. D'Amico and F.G. Bollinger, J. Heterocyclic Chem., 25, 1183-