Synthesis of hydrazide-hydrazone derivatives and their evaluation of antidepressant, sedative and analgesic agents
dc.Affiliation | October University for modern sciences and Arts (MSA) | |
dc.contributor.author | Mohareb R.M. | |
dc.contributor.author | El-Sharkawy K.A. | |
dc.contributor.author | Hussein M.M. | |
dc.contributor.author | El-Sehrawi H.M. | |
dc.contributor.other | Faculty of Pharmacy | |
dc.contributor.other | Organic Chemistry Department | |
dc.contributor.other | October University for Modern Sciences and Arts (MSA) | |
dc.contributor.other | El-Wahat Road | |
dc.contributor.other | 6 October City | |
dc.contributor.other | Egypt; Department of Chemistry | |
dc.contributor.other | Faculty of Science | |
dc.contributor.other | Cairo University | |
dc.contributor.other | Giza | |
dc.contributor.other | A. R | |
dc.contributor.other | Egypt; Faculty of Pharmacy (Girls) | |
dc.contributor.other | Pharmaceutical Chemistry Department | |
dc.contributor.other | Al-Azhar University | |
dc.contributor.other | Nasr City | |
dc.contributor.other | Cairo | |
dc.contributor.other | A. R | |
dc.contributor.other | Egypt | |
dc.date.accessioned | 2020-01-25T19:58:33Z | |
dc.date.available | 2020-01-25T19:58:33Z | |
dc.date.issued | 2010 | |
dc.description | Scopus | |
dc.description.abstract | The reaction of cyanoacetylhydrazine (1) with ?-bromo(4-methoxyacetophenone) (2) gave the hydrazide-hydrazone derivative 3. Compound 3 reacted with either potassium cyanide or potassium thiocyanide to give the cyanide or thiocyanide derivatives 4a or 4b respectively. The reaction of compound 3 with either hydrazine hydrate or phenylhydrazine gave the hydrazine derivatives 6a or 6b respectively. The latter compounds underwent a series of heterocyclization when react with different reagents to give 1,3,4-triazine and pyridine derivatives. The antidepressant, sedative and analgesic activities of the newly synthesized products were evaluated. | en_US |
dc.identifier.doi | https://doi.org/ | |
dc.identifier.issn | 9751459 | |
dc.identifier.other | https://doi.org/ | |
dc.identifier.uri | https://t.ly/w1mAx | |
dc.language.iso | English | en_US |
dc.relation.ispartofseries | Journal of Pharmaceutical Sciences and Research | |
dc.relation.ispartofseries | 2 | |
dc.subject | 1,3,4-triazine | en_US |
dc.subject | Antidepressant | en_US |
dc.subject | Hydrazide-hydrazone | en_US |
dc.subject | Pyridine | en_US |
dc.subject | Sedative | en_US |
dc.subject | 3 cyano 4,6 dimethyl 2 oxo 1 imino (4 methoxy omega hydrazinoacetophenonylidieno)pyridine | en_US |
dc.subject | 3 cyano 6 hydroxy 4 methyl 2 oxo 1 imino(4 methoxy omega hydrazinoacetophenoylidieno)pyridine | en_US |
dc.subject | 4 amino 5 h 6 (4 methoxyphenyl) 3 (alpha phenylhydrazoacetonitrilo) 1,2,4 triazine | en_US |
dc.subject | 4 amino 5 h 6 (4 methoxyphenyl) 3 [alpha (3 cyano 2 hydrazo 4,5,6,7 tetrahydrobenzo[b]thiophene)acetonitrilo] 1,2,4 triazine | en_US |
dc.subject | 4 methoxy omega bromoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | 4 methoxy omega cyanoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | 4 methoxy omega hydrazinoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | 4 methoxy omega phenylhydrazinoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | 4 methoxy omega thiocyanoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | 4 phenylamino 5 h 6 (4 methoxyphenyl) 3 (alpha phenylhydrazoacetonitrilo) 1,2,4 triazine | en_US |
dc.subject | 4 phenylamino 6 (4 methoxyphenyl) 3 [alpha (3 cyano 2 hydrazo 4,5,6,7 tetrahydrobenzo[b]thiopene)acetonitrilo] 1,2,4 triazine | en_US |
dc.subject | alpha benzal 4 methoxy omega hydrazinoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | alpha benzal 4 methoxy omega phenylhydrazinoacetophenone cyanoacetylhydrazone | en_US |
dc.subject | ethyl 4 amino 5 h 6 (4 methoxyphenyl) 3 [alpha (2 hydrazo 4,5,6,7 tetrahydrobenzo[b]thiophene 3 carboxylate)acetonitrilo] 1,2,4 triazine | en_US |
dc.subject | ethyl 4 phenylamino 6 (4 methoxyphenyl) 3 [alpha (2 hydrazo 4,5,6,7 tetrahydrobenzo[b]thiopen 3 carboxylate)acetonitrilo] 1,2,4 triazine | en_US |
dc.subject | hydrazine derivative | en_US |
dc.subject | hydrazone derivative | en_US |
dc.subject | imipramine | en_US |
dc.subject | indometacin | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | analgesic activity | en_US |
dc.subject | animal experiment | en_US |
dc.subject | antidepressant activity | en_US |
dc.subject | article | en_US |
dc.subject | controlled study | en_US |
dc.subject | cyclization | en_US |
dc.subject | drug determination | en_US |
dc.subject | drug mechanism | en_US |
dc.subject | drug megadose | en_US |
dc.subject | drug potency | en_US |
dc.subject | drug screening | en_US |
dc.subject | drug structure | en_US |
dc.subject | drug synthesis | en_US |
dc.subject | experimental mouse | en_US |
dc.subject | female | en_US |
dc.subject | forced swimming test | en_US |
dc.subject | low drug dose | en_US |
dc.subject | male | en_US |
dc.subject | motor activity | en_US |
dc.subject | mouse | en_US |
dc.subject | nonhuman | en_US |
dc.subject | sedation | en_US |
dc.title | Synthesis of hydrazide-hydrazone derivatives and their evaluation of antidepressant, sedative and analgesic agents | en_US |
dc.type | Article | en_US |
dcterms.isReferencedBy | Singh, H., Kapoor, V.K., Paul, D., (1979) Progress In Medicinal Chemistry, 16, pp. 35-149. , DOI:10.1016/S0079-6468(08)70187-5; Mohammed, A.E., Mamdouh, S., Taha, A.M., Sharshira, E.M., (1991) Advances In Heterocyclic Chemistry, 52, pp. 1-153. , DOI:10.1016/S0065-2725(08)60963-0; El-Ashry, E.H., Ibrahim, E.I., (2003) Advances In Heterocyclic Chemistry, 84, pp. 71-190; Almeida, P.E., Ramos, D.F., Bonacorso, H.G., Iglesia, A.I., Oliveira, M.R., Coelho, T., Navarini, J., Martins, M.A., (2008) J. of Antimicrobial Agents, 32, pp. 139-144; Contelles, J.M., Mayoral, E.P., Ballesteros, P., (2008) Comprehensive Heterocyclic Chemistry, III, pp. 100-306. , 008044992-0.01005-1, Chapter 10.05; Kumar, P., Narasimhan, B., Sharma, D., Vikramjeet Judge, V., Narang, R., (2009) Eur.J. of Med. Chem., 44, pp. 1853-1863. , DOI:10.1016/j.ejmech.2008.10.034; Sherman, A.R., (2008) Comprehensive Heterocyclic Chemistry, III, pp. 263-338. , Chapter 10.06; Saeed, A., Amara Mumtaz, A., (2008) Chinese Chemical Letters, 19, pp. 1305-1308. , DOI:10.1016/j.cclet.2008.07.017; Trofimov, B.A., Mal'kina, A.G., Borisova, A.P., Nosyreva, V.V., Shemyakina, O.A., Olga, N.K., Shilov, G.V., Dyachenko, O.A., (2008) Tetrahedron Lett., 49, pp. 3104-3107. , DOI:10.1016/j.tetlet.2008.03.046; Xia, Y., Fan, C.D., Zhao, B.X., Zhao, J., Shin, D.S., Jun-Ying Miao, J.Y., (2008) Eur. J. OfMed. Chem., 43, pp. 2347-2353. , DOI:10.1016/j.ejmech.2008.01.021; Zheng, L.W., Wu, L.L., Zhao, B.X., Dong, W.L., Miao, J.Y., (2009) Bioorg. & Med.Chem., 17, pp. 1957-1962. , DOI:10.1016/j.bmc.2009.01.037; Sriram, D., Yogeeswari, P., Devakaram, R.V., (2006) Bioorg. & Med. Chem., 14, pp. 3113-3118. , DOI:10.1016/j.bmc.2005.12.042; Abou-Melha, K., (2008) S. Mol. and Biomol.Spectr., 70, pp. 162-170. , DOI:10.1016/j.saa.2007.07.023; El-Tabl, A.S., El-Saied, F.A., Plass, W., Al-Hakim, A.N., (2008) Mol. and Biomol. Spectr., 71, pp. 90-99. , DOI:10.1016/j.saa.2007.11.011; Joshi, S.D., Vagdevi, H.M., Vaidya, V.P., Gadaginamath, G.S., (2008) Eur. J. of Med. Chem., 43, pp. 1090-1996. , DOI:10.1016/j.ejmech.2007.11.016; K���kg�zel, G., Kocatepe, A., Clercq, E.D., ?ahin, F., Medine, G., (2006) Eur. J. of Med.Chem., 41, pp. 353-359. , DOI:10.1016/j.ejmech.2005.11.005; Petra, K.P., Klime�, Z.M., (2008) J. of Pharm.and Biomed. Anal., 47, pp. 360-370. , DOI:10.1016/j.jpba.2008.01.011; Mohareb, R.M., Ho, J.Z., Alfarouk, F.O., (2007) J of The Chin. Chem. Soc., 54, pp. 1053-1066 | |
dcterms.source | Scopus |