Utilizing of 4-(benzothiazol-2-yl)phenylamine as a precursor of bioactive agents

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dc.contributor.author A.Shaaban, Mohamed
dc.contributor.author M.Al Badry, Ossama
dc.contributor.author M.Kamal, Aliaa
dc.contributor.author A.Abd El-Gawad, Mohamd
dc.date.accessioned 2019-10-21T07:19:31Z
dc.date.available 2019-10-21T07:19:31Z
dc.date.issued 2012
dc.identifier.citation [1] T.D.Bradshaw, M.F.G.Stevens, A.D.Westwell; Current Med.Chem., 8, 203-210 (2001). [2] A.Monks, E.Harris, C.Hose, J.Connelly, E.A.Sausville; Molecular Pharmacology, 63, 766- 772 (2003). [3] E.Brantley, V.Trapani, M.C.Alley, C.D.Hose, T.D.Bradshaw, M.F.G.Stevens, E.A.Sausville, S.F.Stinson; DrugMetabolismandDisposition, 32, 1392-1401 (2004). [4] A.Waliqvist, J.Connelly, E.A.Sausville,D.G.Covell, A.Monks; Molecular Pharmacology, 69, 737-748 (2006). [5] C.O.Leong, M.Suggitt, D.J.Swaine, M.C.Bibby, M.F.G.Stevens, T.D.Bradshaw; Molecular Cancer Therapeutics, 3, 1585-1592 (2004). [6] Y.W.Chen, J.E.Cleaver, F.Hanaoka, C.F.Chang; K.Chou; Molecular Cancer Research, 4, 257-265 (2006). [7] E.L.Luzina, A.V.Popov; Eur.J.Med.Chem., 44, 4944-4953 (2009). [8] B.Soni, M.S.Ranawat, R.Sharma, A.Bhandari, S.Sharma; Eur.J.Med.Chem., 45, 2938-2942 (2010). [9] S.Bondock,W.Fadaly,M.A.Metwally; Eur.J.Med. Chem., 45, 3692-3701 (2010). [10] S.Bondock,W.Fadaly,M.A.Metwally; Eur.J.Med. Chem., 44, 4813-4818 (2009). [11] A.E.Rashad, A.H.Shamroukh, M.I.Hegab, H.M.Awad; Acta Chim.Slov., 52, 429-434 (2005). [12] M.Cacic, M.Trkovnik, F.Cacic, E.H.Schon; Molecules, 11, 134-147 (2006). [13] N.Agarwal, P.Srivastava, S.K.Raghuwanshi, D.N.Upadhyay, S.Smha, P.K.Shukia, V.Ram; J.Bioorg.Med.Chem., 10, 869-874 (2002). [14] P.Sharma,A.Kumar,M.Sharma; Eur.J.Med.Chem., 41, 833-840 (2006). [15] P.Vicini, A.Geronikaki, K.Anastasia, M.Incerti, F.Zam; Bioorg.Med.Chem., 14, 3859-3864 (2006). [16] S.Bondock, W.Khalifa, A.A.Fadda; Eur.J.Med. Chem., 42, 948-954 (2007). [17] V.Patil, K.Tilekar, S.Mehendale-Munj, R.Mohan, C.S.Ramaa; Eur.J.Med.Chem., 45, 4539-4544 (2010). [18] D.Havrylyuk, L.Mosula, B.Zimenkovsky, O.Vasylenko,A.Gzella,R.Lesyk; Eur.J.Med.Chem., 45, 5012-5021 (2010). [19] T.Kline, K.C.Barry, S.R.Jackson, H.B.Felise, H.V.Nguyen, S.I.Miller; Bioorg.Med.Chem.Lett., 19, 1340-1343 (2009). [20] S.P.Mohammed; Bull.Fac.Pharm.Cairo Uinv., 37, 33-40 (1999). [21] S.E.Abbas, M.M.Hanna, A.H.Abou Sier, M.A.H.Ramadan; Egypt J.Pharm.Sci., 34, 195-205 (1993). [22] B.Kahveci, O.Bekircan, S.A.Karaoghlu; Indain J.Chem.B, 44b, 2614-2617 (2005). [23] O.Pintilie, L.Profire,V.Sunel,M.Popa,A.Pui;Molecules, 12, 103-113 (2007). [24] M.A.Shaaban, O.M.Al Badry, A.M.Kamal, M.A.W.Abd El-Gawad; J.Chem.Reseach, 4, 715- 718 (2008). [25] G.Bruno, L.Costantino, C.Curinga, R.Maccari, F.Monforte, F.Nicolo , R.Ottana , M.G.Vigoritac; Bioorg.Med.Chem., 10, 1077-1084 (2002). [26] R.Ottana , R.Maccari, M.L.Barreca, G.Bruno, A.Rotondo, A.Rossi, G.Chiricosta, R.Di Paola, L.Sautebin, S.Cuzzocrea, M.G.Vigorita; Bioorg. Med.Chem., 13, 4243-4252 (2005). [27] T.O.Richardson,V.P.Shambhag, K.Adair, S.Smith; J.Heterocyclic Chem., 35, 1301 (1998). en_US
dc.identifier.issn 0974 - 7516
dc.identifier.other https://doi.org/
dc.identifier.uri https://t.ly/WE9rm
dc.description.abstract Several heterocyclic compounds show either anticancer or antimicrobial activity, the intial goal of this study was directed towards combining some of those heterocyclic moieties- that have either activity- together to test whether the newly formed compounds will demonstrate both activity or one activity will predominate over the other or both activity will deminish. This was accomplished via Scheme 1 and Scheme 2 where diazotization of 4-(benzothiazol-2-yl)phenylamine 1 followed by reacting this functionalized hydrazone with a variety of binucleophiles to give the key intermediates that reacted with amino reagents viz. hydrazine, urea or thiourea to yield some of the goal compounds (Scheme 1). Reacting compound 1with carbonyl or isothiocyanate reagents followed by cyclization of the given key intermediates afforeded a set of novel target compounds (Scheme 2). These final compunds were tested for in vitro antimicrobial and anticancer activity. Two compounds showed both antimicrobial and anticancer activity while the other compounds were highly active either as antimicrobial only or as anticancer only. en_US
dc.description.sponsorship Organic CHEMISTRY en_US
dc.language.iso en en_US
dc.publisher Organic CHEMISTRY en_US
dc.relation.ispartofseries Organic CHEMISTRY;Volume 8 Issue 9
dc.subject benzothiazol en_US
dc.subject phenylamine en_US
dc.subject Pharmacophores en_US
dc.subject Anticancer en_US
dc.subject Antimicrobial en_US
dc.subject Improving chemotherapy regimen design en_US
dc.title Utilizing of 4-(benzothiazol-2-yl)phenylamine as a precursor of bioactive agents en_US
dc.type Article en_US
dc.identifier.doi https://doi.org/
dc.Affiliation October University for modern sciences and Arts (MSA)


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